Name

CMAP Signatures of Differentially Expressed Genes for Small Molecules Dataset

From Connectivity Map

mRNA expression profiles for cell lines following chemical perturbation

GEO Signatures of Differentially Expressed Genes for Small Molecules Dataset

From Gene Expression Omnibus

mRNA expression profiles for cell lines or tissues following small molecule perturbation

LINCS L1000 CMAP Signatures of Differentially Expressed Genes for Small Molecules Dataset (Archived)

From LINCS L1000 Connectivity Map

mRNA expression profiles for cell lines following small molecule perturbation

MS Gene

multiple sclerosis

SHANK3 Gene

SH3 and multiple ankyrin repeat domains 3

This gene is a member of the Shank gene family. Shank proteins are multidomain scaffold proteins of the postsynaptic density that connect neurotransmitter receptors, ion channels, and other membrane proteins to the actin cytoskeleton and G-protein-coupled signaling pathways. Shank proteins also play a role in synapse formation and dendritic spine maturation. Mutations in this gene are a cause of autism spectrum disorder (ASD), which is characterized by impairments in social interaction and communication, and restricted behavioral patterns and interests. Mutations in this gene also cause schizophrenia type 15, and are a major causative factor in the neurological symptoms of 22q13.3 deletion syndrome, which is also known as Phelan-McDermid syndrome. Additional isoforms have been described for this gene but they have not yet been experimentally verified. [provided by RefSeq, Mar 2012]

SHANK2 Gene

SH3 and multiple ankyrin repeat domains 2

This gene encodes a protein that is a member of the Shank family of synaptic proteins that may function as molecular scaffolds in the postsynaptic density of excitatory synapses. Shank proteins contain multiple domains for protein-protein interaction, including ankyrin repeats, and an SH3 domain. This particular family member contains a PDZ domain, a consensus sequence for cortactin SH3 domain-binding peptides and a sterile alpha motif. The alternative splicing demonstrated in Shank genes has been suggested as a mechanism for regulating the molecular structure of Shank and the spectrum of Shank-interacting proteins in the postsynaptic densities of the adult and developing brain. Alterations in the encoded protein may be associated with susceptibility to autism spectrum disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]

SHANK1 Gene

SH3 and multiple ankyrin repeat domains 1

This gene encodes a member of the SHANK (SH3 domain and ankyrin repeat containing) family of proteins. Members of this family act as scaffold proteins that are required for the development and function of neuronal synapses. Deletions in this gene may be associated with autism spectrum disorder in males. [provided by RefSeq, Apr 2016]

EXT3 Gene

exostoses (multiple) 3

MMDFS Gene

Multiple mitochondrial dysfunctions syndrome

MEN1 Gene

multiple endocrine neoplasia I

This gene encodes menin, a tumor suppressor associated with a syndrome known as multiple endocrine neoplasia type 1. Menin is a scaffold protein that functions in histone modification and epigenetic gene regulation. It is thought to regulate several pathways and processes by altering chromatin structure through the modification of histones. [provided by RefSeq, May 2019]

MCTP1 Gene

multiple C2 domains, transmembrane 1

Enables calcium ion binding activity. Predicted to be involved in several processes, including modulation of chemical synaptic transmission; negative regulation of endocytosis; and negative regulation of response to oxidative stress. Located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

MCTP2 Gene

multiple C2 domains, transmembrane 2

Enables calcium ion binding activity. Predicted to be involved in regulation of neurotransmitter secretion. Located in cytosol; membrane; and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025]

MMEDF Gene

Macrocephaly with multiple epiphyseal dysplasia and distinctive facies

MEGF8 Gene

multiple EGF-like-domains 8

The protein encoded by this gene is a single-pass type I membrane protein of unknown function that contains several EGF-like domains, Kelch repeats, and PSI domains. Defects in this gene are a cause of Carpenter syndrome 2. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012]

CNC2 Gene

Carney complex type 2, multiple neoplasia and lentiginosis

RBPMS2 Gene

RNA binding protein with multiple splicing 2

The protein encoded by this gene is a member of the RNA recognition motif (RRM)-containing protein family and is involved in the development and dedifferentiation of digestive smooth muscle cells. The encoded protein functions as a homodimer and indirectly inhibits the bone morphogenetic protein pathway. [provided by RefSeq, Aug 2016]

MCFD2P1 Gene

multiple coagulation factor deficiency 2 pseudogene 1

MINPP1 Gene

multiple inositol-polyphosphate phosphatase 1

This gene encodes multiple inositol polyphosphate phosphatase; an enzyme that removes 3-phosphate from inositol phosphate substrates. It is the only enzyme known to hydrolzye inositol pentakisphosphate and inositol hexakisphosphate. This enzyme also converts 2,3 bisphosphoglycerate (2,3-BPG) to 2-phosphoglycerate; an activity formerly thought to be exclusive to 2,3-BPG synthase/2-phosphatase (BPGM) in the Rapoport-Luebering shunt of the glycolytic pathway.[provided by RefSeq, Sep 2009]

RBPMSLP Gene

RNA binding protein with multiple splicing-like pseudogene

MS4 Gene

Multiple sclerosis, susceptiblity to, 4

MS3 Gene

Multiple sclerosis, susceptibility to, 3

MS2 Gene

Multiple sclerosis, susceptibility to, 2

CSMD2 Gene

CUB and Sushi multiple domains 2

The protein encoded by this gene is thought to be involved in the control of complement cascade of the immune system. Defects in this gene have been associated with schizophrenia. This gene may act as a tumor suppressor for colorectal cancer. [provided by RefSeq, Jan 2020]

CSMD3 Gene

CUB and Sushi multiple domains 3

Predicted to be involved in regulation of dendrite development. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025]

CSMD1 Gene

CUB and Sushi multiple domains 1

Predicted to act upstream of or within several processes, including learning or memory; mammary gland branching involved in pregnancy; and reproductive structure development. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

LOC105373985 Gene

multiple epidermal growth factor-like domains protein 6

MFT2 Gene

Trichoepithelioma, multiple familial, 2

EGFL7 Gene

EGF-like-domain, multiple 7

This gene encodes a secreted endothelial cell protein that contains two epidermal growth factor-like domains. The encoded protein may play a role in regulating vasculogenesis. This protein may be involved in the growth and proliferation of tumor cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]

EGFL6 Gene

EGF-like-domain, multiple 6

This gene encodes a member of the epidermal growth factor (EGF) repeat superfamily. Members of this superfamily are characterized by the presence of EGF-like repeats and are often involved in the regulation of cell cycle, proliferation, and developmental processes. The gene product contains a signal peptide, suggesting that it is secreted; an EGF repeat region consisting of 4 complete EGF-like repeats and 1 partial EGF-like repeat, 3 of which have a calcium-binding consensus sequence; an arg-gly-asp integrin association motif; and a MAM domain, which is believed to have an adhesive function. This gene is expressed early during development, and its expression has been detected in lung and meningioma tumors. [provided by RefSeq, Jul 2008]

EGFL8 Gene

EGF-like-domain, multiple 8

Predicted to enable signaling receptor binding activity. Predicted to be involved in vasculogenesis. Predicted to be active in cell surface and extracellular region. [provided by Alliance of Genome Resources, Mar 2025]

MEGF9 Gene

multiple EGF-like-domains 9

Predicted to enable small GTPase binding activity. Predicted to be involved in regulation of actin filament polymerization. Predicted to be located in basement membrane and membrane. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025]

MEGF6 Gene

multiple EGF-like-domains 6

Predicted to enable calcium ion binding activity and scavenger receptor activity. Predicted to be involved in vesicle-mediated transport. Predicted to be located in extracellular region. [provided by Alliance of Genome Resources, Mar 2025]

CHDT3 Gene

Congenital heart defects, multiple types, 3

EXTL2P1 Gene

exostoses (multiple)-like 2 pseudogene 1

ODPF Gene

Osseous dysplasia, digital, with facial pigmentary defects and multiple frenula

MPDZ Gene

multiple PDZ domain protein

The protein encoded by this gene has multiple PDZ domains, which are hallmarks of protein-protein interactions. The encoded protein is known to interact with the HTR2C receptor and may cause it to clump at the cell surface. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015]

RBPMS Gene

RNA binding protein with multiple splicing

This gene encodes a member of the RNA recognition motif family of RNA-binding proteins. The RNA recognition motif is between 80-100 amino acids in length and family members contain one to four copies of the motif. The RNA recognition motif consists of two short stretches of conserved sequence, as well as a few highly conserved hydrophobic residues. The encoded protein has a single, putative RNA recognition motif in its N-terminus. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2013]

MCFD2 Gene

multiple coagulation factor deficiency 2

This gene encodes a soluble luminal protein with two calmodulin-like EF-hand motifs at its C-terminus. This protein forms a complex with LMAN1 (lectin mannose binding protein 1; also known as ERGIC-53) that facilitates the transport of coagulation factors V (FV) and VIII (FVIII) from the endoplasmic reticulum to the Golgi apparatus via an endoplasmic reticulum Golgi intermediate compartment (ERGIC). Mutations in this gene cause combined deficiency of FV and FVIII (F5F8D); a rare autosomal recessive bleeding disorder characterized by mild to moderate bleeding and coordinate reduction in plasma FV and FVIII levels. This protein has also been shown to maintain stem cell potential in adult central nervous system and is a marker for testicular germ cell tumors. The 3' UTR of this gene contains a transposon-like human repeat element named 'THE 1'. A processed RNA pseudogene of this gene is on chromosome 6p22.1. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Apr 2016]

MEGF10 Gene

multiple EGF-like-domains 10

This gene encodes a member of the multiple epidermal growth factor-like domains protein family. The encoded protein plays a role in cell adhesion, motility and proliferation, and is a critical mediator of apoptotic cell phagocytosis as well as amyloid-beta peptide uptake in the brain. Expression of this gene may be associated with schizophrenia, and mutations in this gene are a cause of early-onset myopathy, areflexia, respiratory distress, and dysphagia (EMARDD) as well as congenital myopathy with minicores. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Apr 2012]

MEGF11 Gene

multiple EGF-like-domains 11

Predicted to be involved in homotypic cell-cell adhesion and retina layer formation. Predicted to be located in basolateral plasma membrane. [provided by Alliance of Genome Resources, Mar 2025]

RNU5B-1 Gene

RNA, U5B small nuclear 1

Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U5 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

SNRPCP6 Gene

small nuclear ribonucleoprotein polypeptide C pseudogene 6

LOC101928952 Gene

serine palmitoyltransferase small subunit A pseudogene

RNU6-67P Gene

RNA, U6 small nuclear 67, pseudogene

RNU7-36P Gene

RNA, U7 small nuclear 36 pseudogene

SNORA81 Gene

small nucleolar RNA, H/ACA box 81

Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA81, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]

SNORA84 Gene

small nucleolar RNA, H/ACA box 84

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SGSM3 Gene

small G protein signaling modulator 3

Enables GTPase activator activity and small GTPase binding activity. Involved in several processes, including Rap protein signal transduction; positive regulation of GTPase activity; and regulation of Rab protein signal transduction. Located in cytosol. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-14 Gene

small nucleolar RNA, C/D box 115-14

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-16 Gene

small nucleolar RNA, C/D box 115-16

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-17 Gene

small nucleolar RNA, C/D box 115-17

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-10 Gene

small nucleolar RNA, C/D box 115-10

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU1-16P Gene

RNA, U1 small nuclear 16, pseudogene

KRR1 Gene

KRR1, small subunit (SSU) processome component, homolog (yeast)

Enables RNA binding activity. Involved in ribosomal small subunit biogenesis. Located in chromosome; intercellular bridge; and nuclear lumen. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-53P Gene

RNA, U7 small nuclear 53 pseudogene

RNU5A-5P Gene

RNA, U5A small nuclear 5, pseudogene

SNORD48 Gene

small nucleolar RNA, C/D box 48

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD90 Gene

small nucleolar RNA, C/D box 90

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD41 Gene

small nucleolar RNA, C/D box 41

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD47 Gene

small nucleolar RNA, C/D box 47

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD44 Gene

small nucleolar RNA, C/D box 44

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD93 Gene

small nucleolar RNA, C/D box 93

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD4B Gene

small nucleolar RNA, C/D box 4B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD4A Gene

small nucleolar RNA, C/D box 4A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

LOC100133102 Gene

ras-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2) pseudogene

LOC100422227 Gene

small ubiquitin-like modifier 1 pseudogene

U2AF1L4 Gene

U2 small nuclear RNA auxiliary factor 1-like 4

Predicted to enable pre-mRNA 3'-splice site binding activity. Predicted to be involved in mRNA splicing, via spliceosome. Predicted to be located in nucleoplasm. Predicted to be part of U2AF complex and spliceosomal complex. [provided by Alliance of Genome Resources, Mar 2025]

RNU2-6P Gene

RNA, U2 small nuclear 6, pseudogene

SNORD91B Gene

small nucleolar RNA, C/D box 91B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD91A Gene

small nucleolar RNA, C/D box 91A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

LOC402230 Gene

small nuclear ribonucleoprotein 27kDa (U4/U6.U5) pseudogene

SNORD115-6 Gene

small nucleolar RNA, C/D box 115-6

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-7 Gene

small nucleolar RNA, C/D box 115-7

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-4 Gene

small nucleolar RNA, C/D box 115-4

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-1 Gene

small nucleolar RNA, C/D box 115-1

This gene encodes a small nucleolar RNA (snoRNA) that is found clustered with dozens of other similar snoRNAs on chromosome 15. These genes are found mostly within introns of the IC-SNURF-SNRPN transcript, which is paternally imprinted and from the Prader-Willi/Angelman syndrome (PWS) region. This gene has been designated as copy 1 of the cluster and may be involved in the regulation of RNA editing and/or alternative splicing of the serotonin receptor 2C (HTR2C) transcript. This gene is not thought to play a major role in PWS. [provided by RefSeq, Jul 2008]

LOC100131425 Gene

LSM5 homolog, U6 small nuclear RNA associated (S. cerevisiae) pseudogene

LOC100820733 Gene

LSM2 homolog, U6 small nuclear RNA associated (S. cerevisiae) pseudogene

RNU7-1 Gene

RNA, U7 small nuclear 1

Implicated in Aicardi-Goutieres syndrome. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-46P Gene

RNA, U6 small nuclear 46, pseudogene

SERF2 Gene

small EDRK-rich factor 2

Involved in protein destabilization. Predicted to be located in cytosol and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD45A Gene

small nucleolar RNA, C/D box 45A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

LOC101929101 Gene

carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene

SNORD111B Gene

small nucleolar RNA, C/D box 111B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

LOC100631265 Gene

M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene

LOC100631267 Gene

M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene

LOC100631266 Gene

M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene

LOC100631268 Gene

M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene

RNU5E-6P Gene

RNA, U5E small nuclear 6, pseudogene

RNU7-24P Gene

RNA, U7 small nuclear 24 pseudogene

SNRPD3 Gene

small nuclear ribonucleoprotein D3 polypeptide 18kDa

This gene encodes a core component of the spliceosome, which is a nuclear ribonucleoprotein complex that functions in pre-mRNA splicing. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]

SNRPD2 Gene

small nuclear ribonucleoprotein D2 polypeptide 16.5kDa

The protein encoded by this gene belongs to the small nuclear ribonucleoprotein core protein family. It is required for pre-mRNA splicing and small nuclear ribonucleoprotein biogenesis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2009]

SNRPD1 Gene

small nuclear ribonucleoprotein D1 polypeptide 16kDa

This gene encodes a small nuclear ribonucleoprotein that belongs to the SNRNP core protein family. The protein may act as a charged protein scaffold to promote SNRNP assembly or strengthen SNRNP-SNRNP interactions through nonspecific electrostatic contacts with RNA. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2014]

MPHOSPH10 Gene

M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein)

This gene encodes a protein that is phosphorylated during mitosis. The protein localizes to the nucleolus during interphase and to the chromosomes during M phase. The protein associates with the U3 small nucleolar ribonucleoprotein 60-80S complexes and may be involved in pre-rRNA processing. [provided by RefSeq, Dec 2010]

LOC100131877 Gene

small EDRK-rich factor 2 pseudogene

RNU1-28P Gene

RNA, U1 small nuclear 28, pseudogene

RNU1-13P Gene

RNA, U1 small nuclear 13, pseudogene

RNU7-5P Gene

RNA, U7 small nuclear 5 pseudogene

SPRR4 Gene

small proline-rich protein 4

Predicted to be involved in keratinization. Predicted to be located in cell cortex. [provided by Alliance of Genome Resources, Mar 2025]

SPRR3 Gene

small proline-rich protein 3

Predicted to enable structural molecule activity. Predicted to be involved in keratinocyte differentiation and wound healing. Located in Golgi apparatus and perinuclear region of cytoplasm. [provided by Alliance of Genome Resources, Mar 2025]

RNU6ATAC5P Gene

RNA, U6atac small nuclear 5, pseudogene

LSM8 Gene

LSM8 homolog, U6 small nuclear RNA associated (S. cerevisiae)

This gene encodes a member of the like-Sm family of proteins. The encoded protein consists of a closed barrel shape, made up of five anti-parallel beta strands and an alpha helix. This protein partners with six paralogs to form a heteroheptameric ring which transiently binds U6 small nuclear RNAs and is involved in the general maturation of RNA in the nucleus. [provided by RefSeq, Jan 2010]

LSM4 Gene

LSM4 homolog, U6 small nuclear RNA associated (S. cerevisiae)

This gene encodes a member of the LSm family of RNA-binding proteins. LSm proteins form stable heteromers that bind specifically to the 3'-terminal oligo(U) tract of U6 snRNA and may play a role in pre-mRNA splicing by mediating U4/U6 snRNP formation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]

LSM5 Gene

LSM5 homolog, U6 small nuclear RNA associated (S. cerevisiae)

Sm-like proteins were identified in a variety of organisms based on sequence homology with the Sm protein family (see SNRPD2; MIM 601061). Sm-like proteins contain the Sm sequence motif, which consists of 2 regions separated by a linker of variable length that folds as a loop. The Sm-like proteins are thought to form a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing.[supplied by OMIM, Apr 2004]

LSM6 Gene

LSM6 homolog, U6 small nuclear RNA associated (S. cerevisiae)

Sm-like proteins were identified in a variety of organisms based on sequence homology with the Sm protein family (see SNRPD2; MIM 601061). Sm-like proteins contain the Sm sequence motif, which consists of 2 regions separated by a linker of variable length that folds as a loop. The Sm-like proteins are thought to form a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing.[supplied by OMIM, Apr 2004]

SNRPGP9 Gene

small nuclear ribonucleoprotein polypeptide G pseudogene 9

SNRPGP7 Gene

small nuclear ribonucleoprotein polypeptide G pseudogene 7

SNRPGP6 Gene

small nuclear ribonucleoprotein polypeptide G pseudogene 6

SNRPGP5 Gene

small nuclear ribonucleoprotein polypeptide G pseudogene 5

SNRPGP4 Gene

small nuclear ribonucleoprotein polypeptide G pseudogene 4

SNRPGP1 Gene

small nuclear ribonucleoprotein polypeptide G pseudogene 1

LOC100129534 Gene

small nuclear ribonucleoprotein polypeptide N pseudogene

LOC101927923 Gene

small integral membrane protein 12-like

LOC100131747 Gene

small EDRK-rich factor 2 pseudogene

SNORD12C Gene

small nucleolar RNA, C/D box 12C

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD12B Gene

small nucleolar RNA, C/D box 12B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD123 Gene

small nucleolar RNA, C/D box 123

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD127 Gene

small nucleolar RNA, C/D box 127

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD124 Gene

small nucleolar RNA, C/D box 124

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-62P Gene

RNA, U7 small nuclear 62 pseudogene

RNU6-79P Gene

RNA, U6 small nuclear 79, pseudogene

RNU4-7P Gene

RNA, U4 small nuclear 7, pseudogene

RNU6-8 Gene

RNA, U6 small nuclear 8

Predicted to enable U4 snRNA binding activity. Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U6 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-9 Gene

RNA, U6 small nuclear 9

Predicted to enable U4 snRNA binding activity. Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U6 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-7 Gene

RNA, U6 small nuclear 7

Predicted to enable U4 snRNA binding activity. Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U6 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-1 Gene

RNA, U6 small nuclear 1

Predicted to enable U4 snRNA binding activity. Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U6 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-2 Gene

RNA, U6 small nuclear 2

Predicted to enable U4 snRNA binding activity. Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U6 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-69P Gene

RNA, U6 small nuclear 69, pseudogene

SNORA9 Gene

small nucleolar RNA, H/ACA box 9

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA8 Gene

small nucleolar RNA, H/ACA box 8

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA1 Gene

small nucleolar RNA, H/ACA box 1

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA4 Gene

small nucleolar RNA, H/ACA box 4

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA6 Gene

small nucleolar RNA, H/ACA box 6

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU1-20P Gene

RNA, U1 small nuclear 20, pseudogene

LOC100421121 Gene

small G protein signaling modulator 1 pseudogene

RRP9 Gene

ribosomal RNA processing 9, small subunit (SSU) processome component, homolog (yeast)

This gene encodes a member of the WD-repeat protein family. The encoded protein is a component of the nucleolar small nuclear ribonucleoprotein particle (snoRNP) and is essential for 18s rRNA processing during ribosome synthesis. It contains seven WD domains required for nucleolar localization and specific interaction with the U3 small nucleolar RNA (U3 snoRNA). [provided by RefSeq, Oct 2012]

SMIM13 Gene

small integral membrane protein 13

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM12 Gene

small integral membrane protein 12

Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025]

SMIM11 Gene

small integral membrane protein 11

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM10 Gene

small integral membrane protein 10

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM17 Gene

small integral membrane protein 17

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM15 Gene

small integral membrane protein 15

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM14 Gene

small integral membrane protein 14

Predicted to act upstream of or within blastocyst hatching. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Mar 2025]

SMIM19 Gene

small integral membrane protein 19

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM18 Gene

small integral membrane protein 18

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-47P Gene

RNA, U7 small nuclear 47 pseudogene

RNU7-86P Gene

RNA, U7 small nuclear 86 pseudogene

SNORD121B Gene

small nucleolar RNA, C/D box 121B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD121A Gene

small nucleolar RNA, C/D box 121A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-13P Gene

RNA, U7 small nuclear 13 pseudogene

RNU6-36P Gene

RNA, U6 small nuclear 36, pseudogene

RNU4ATAC2P Gene

RNA, U4atac small nuclear 2, pseudogene

RNU6-64P Gene

RNA, U6 small nuclear 64, pseudogene

SNRNP200 Gene

small nuclear ribonucleoprotein 200kDa (U5)

Pre-mRNA splicing is catalyzed by the spliceosome, a complex of specialized RNA and protein subunits that removes introns from a transcribed pre-mRNA segment. The spliceosome consists of small nuclear RNA proteins (snRNPs) U1, U2, U4, U5 and U6, together with approximately 80 conserved proteins. U5 snRNP contains nine specific proteins. This gene encodes one of the U5 snRNP-specific proteins. This protein belongs to the DEXH-box family of putative RNA helicases. It is a core component of U4/U6-U5 snRNPs and appears to catalyze an ATP-dependent unwinding of U4/U6 RNA duplices. Mutations in this gene cause autosomal-dominant retinitis pigmentosa. Alternatively spliced transcript variants encoding different isoforms have been found, but the full-length nature of these variants has not been determined. [provided by RefSeq, Mar 2010]

RNU5B-5P Gene

RNA, U5B small nuclear 5, pseudogene

RNU6-63P Gene

RNA, U6 small nuclear 63, pseudogene

SNORA74A Gene

small nucleolar RNA, H/ACA box 74A

Predicted to be involved in RNA processing. Part of box H/ACA RNP complex. [provided by Alliance of Genome Resources, Mar 2025]

SNORA74B Gene

small nucleolar RNA, H/ACA box 74B

Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA74B, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]

RNU7-54P Gene

RNA, U7 small nuclear 54 pseudogene

RNU5A-2P Gene

RNA, U5A small nuclear 2, pseudogene

SNORD115-43 Gene

small nucleolar RNA, C/D box 115-43

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-41 Gene

small nucleolar RNA, C/D box 115-41

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-47 Gene

small nucleolar RNA, C/D box 115-47

SNORD1A Gene

small nucleolar RNA, C/D box 1A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD1B Gene

small nucleolar RNA, C/D box 1B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD1C Gene

small nucleolar RNA, C/D box 1C

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD16 Gene

small nucleolar RNA, C/D box 16

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD10 Gene

small nucleolar RNA, C/D box 10

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD11 Gene

small nucleolar RNA, C/D box 11

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD19 Gene

small nucleolar RNA, C/D box 19

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-32P Gene

RNA, U7 small nuclear 32 pseudogene

SNORD43 Gene

small nucleolar RNA, C/D box 43

Intronic regions of ribosomal protein genes can harbor noncoding small nucleolar RNAs (snoRNAs), like SNORD43, which are generated during pre-mRNA processing. snoRNAs form part of the small nucleolar ribonucleoprotein particles (snoRNPs) involved in pre-rRNA processing and modification. snoRNAs of the box C/D class, like SNORD43, function in 2-prime-O-ribose methylation of rRNAs (Duga et al., 2000 [PubMed 10684968]).[supplied by OMIM, Mar 2008]

SNORD46 Gene

small nucleolar RNA, C/D box 46

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-6 Gene

small nucleolar RNA, C/D box 116-6

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNAR-F Gene

small ILF3/NF90-associated RNA F

SNAR-E Gene

small ILF3/NF90-associated RNA E

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SNAR-D Gene

small ILF3/NF90-associated RNA D

KCNN4 Gene

potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 4

The protein encoded by this gene is part of a potentially heterotetrameric voltage-independent potassium channel that is activated by intracellular calcium. Activation is followed by membrane hyperpolarization, which promotes calcium influx. The encoded protein may be part of the predominant calcium-activated potassium channel in T-lymphocytes. This gene is similar to other KCNN family potassium channel genes, but it differs enough to possibly be considered as part of a new subfamily. [provided by RefSeq, Jul 2008]

KCNN3 Gene

potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 3

Action potentials in vertebrate neurons are followed by an afterhyperpolarization (AHP) that may persist for several seconds and may have profound consequences for the firing pattern of the neuron. Each component of the AHP is kinetically distinct and is mediated by different calcium-activated potassium channels. This gene belongs to the KCNN family of potassium channels. It encodes an integral membrane protein that forms a voltage-independent calcium-activated channel, which is thought to regulate neuronal excitability by contributing to the slow component of synaptic AHP. This gene contains two CAG repeat regions in the coding sequence. It was thought that expansion of one or both of these repeats could lead to an increased susceptibility to schizophrenia or bipolar disorder, but studies indicate that this is probably not the case. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2011]

KCNN2 Gene

potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 2

Action potentials in vertebrate neurons are followed by an afterhyperpolarization (AHP) that may persist for several seconds and may have profound consequences for the firing pattern of the neuron. Each component of the AHP is kinetically distinct and is mediated by different calcium-activated potassium channels. The protein encoded by this gene is activated before membrane hyperpolarization and is thought to regulate neuronal excitability by contributing to the slow component of synaptic AHP. This gene is a member of the KCNN family of potassium channel genes. The encoded protein is an integral membrane protein that forms a voltage-independent calcium-activated channel with three other calmodulin-binding subunits. Alternate splicing of this gene results in multiple transcript variants. [provided by RefSeq, May 2013]

KCNN1 Gene

potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 1

Action potentials in vertebrate neurons are followed by an afterhyperpolarization (AHP) that may persist for several seconds and may have profound consequences for the firing pattern of the neuron. Each component of the AHP is kinetically distinct and is mediated by different calcium-activated potassium channels. The protein encoded by this gene is activated before membrane hyperpolarization and is thought to regulate neuronal excitability by contributing to the slow component of synaptic AHP. The encoded protein is an integral membrane protein that forms a voltage-independent calcium-activated channel with three other calmodulin-binding subunits. This gene is a member of the KCNN family of potassium channel genes. [provided by RefSeq, Jul 2008]

RNU7-33P Gene

RNA, U7 small nuclear 33 pseudogene

RNU5D-2P Gene

RNA, U5D small nuclear 2, pseudogene

SNORA33 Gene

small nucleolar RNA, H/ACA box 33

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA32 Gene

small nucleolar RNA, H/ACA box 32

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA31 Gene

small nucleolar RNA, H/ACA box 31

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. Implicated in brain disease. [provided by Alliance of Genome Resources, Mar 2025]

SNORA30 Gene

small nucleolar RNA, H/ACA box 30

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA35 Gene

small nucleolar RNA, H/ACA box 35

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA34 Gene

small nucleolar RNA, H/ACA box 34

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA38 Gene

small nucleolar RNA, H/ACA box 38

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-76P Gene

RNA, U6 small nuclear 76, pseudogene

RNU7-27P Gene

RNA, U7 small nuclear 27 pseudogene

SNRPCP9 Gene

small nuclear ribonucleoprotein polypeptide C pseudogene 9

SNRPCP8 Gene

small nuclear ribonucleoprotein polypeptide C pseudogene 8

SNRPCP3 Gene

small nuclear ribonucleoprotein polypeptide C pseudogene 3

SNRPCP2 Gene

small nuclear ribonucleoprotein polypeptide C pseudogene 2

SNRPCP7 Gene

small nuclear ribonucleoprotein polypeptide C pseudogene 7

SNRPCP4 Gene

small nuclear ribonucleoprotein polypeptide C pseudogene 4

SNAPC3 Gene

small nuclear RNA activating complex, polypeptide 3, 50kDa

Predicted to enable RNA polymerase III type 3 promoter sequence-specific DNA binding activity and bent DNA binding activity. Predicted to contribute to RNA polymerase II cis-regulatory region sequence-specific DNA binding activity and core promoter sequence-specific DNA binding activity. Predicted to be involved in snRNA transcription by RNA polymerase II and snRNA transcription by RNA polymerase III. Located in nuclear body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNAPC2 Gene

small nuclear RNA activating complex, polypeptide 2, 45kDa

This gene encodes a subunit of the snRNA-activating protein complex which is associated with the TATA box-binding protein. The encoded protein is necessary for RNA polymerase II and III dependent small-nuclear RNA gene transcription. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2009]

SNAPC1 Gene

small nuclear RNA activating complex, polypeptide 1, 43kDa

Predicted to enable sequence-specific DNA binding activity. Predicted to be involved in snRNA transcription by RNA polymerase II and snRNA transcription by RNA polymerase III. Located in nucleolus and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025]

SNAPC5 Gene

small nuclear RNA activating complex, polypeptide 5, 19kDa

This gene encodes a subunit of the small nuclear RNA (snRNA)-activating protein complex that plays a role in the transcription of snRNA genes. This complex binds to the promoters of snRNA genes transcribed by either RNA polymerase II or III and recruits other regulatory factors to activate snRNA gene transcription. The encoded protein may play a role in stabilizing this complex. A pseudogene of this gene has been identified on chromosome 6. [provided by RefSeq, Jul 2016]

SNAPC4 Gene

small nuclear RNA activating complex, polypeptide 4, 190kDa

This gene encodes the largest subunit of the small nuclear RNA-activating protein (SNAP) complex. The encoded protein contains a Myb DNA-binding domain, and is essential for RNA polymerase II and III polymerase transcription from small nuclear RNA promoters. A mutation in this gene is associated with ankylosing spondylitis. [provided by RefSeq, Jul 2016]

SNORD98 Gene

small nucleolar RNA, C/D box 98

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD99 Gene

small nucleolar RNA, C/D box 99

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD94 Gene

small nucleolar RNA, C/D box 94

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD95 Gene

small nucleolar RNA, C/D box 95

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD97 Gene

small nucleolar RNA, C/D box 97

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD92 Gene

small nucleolar RNA, C/D box 92

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-21P Gene

RNA, U6 small nuclear 21, pseudogene

UTP14A Gene

UTP14, U3 small nucleolar ribonucleoprotein, homolog A (yeast)

This gene encodes a member of the uridine triphosphate 14 family. As an essential component of a large ribonucleoprotein complex bound to the U3 small nucleolar RNA, the encoded protein is involved in ribosome biogenesis and 18S rRNA synthesis. An autosomal retrotransposed copy of this X-linked gene exists on chromosome 13. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009]

UTP14C Gene

UTP14, U3 small nucleolar ribonucleoprotein, homolog C (yeast)

Predicted to be involved in several processes, including meiotic cell cycle; rRNA processing; and spermatogenesis. Located in cytosol and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU2-3P Gene

RNA, U2 small nuclear 3, pseudogene

RNU7-75P Gene

RNA, U7 small nuclear 75 pseudogene

RNU7-4P Gene

RNA, U7 small nuclear 4 pseudogene

RN7SKP1 Gene

RNA, 7SK small nuclear pseudogene 1

LOC102724525 Gene

carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene

RNU5A-8P Gene

RNA, U5A small nuclear 8, pseudogene

RNU6-53P Gene

RNA, U6 small nuclear 53, pseudogene

RNU6-39P Gene

RNA, U6 small nuclear 39, pseudogene

RNU5F-6P Gene

RNA, U5F small nuclear 6, pseudogene

SNAR-A8 Gene

small ILF3/NF90-associated RNA A8

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

RNU4-4P Gene

RNA, U4 small nuclear 4, pseudogene

SNAR-G1 Gene

small ILF3/NF90-associated RNA G1

SNAR-G2 Gene

small ILF3/NF90-associated RNA G2

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-83P Gene

RNA, U6 small nuclear 83, pseudogene

RNU1-27P Gene

RNA, U1 small nuclear 27, pseudogene

RNU6-48P Gene

RNA, U6 small nuclear 48, pseudogene

RNU1-18P Gene

RNA, U1 small nuclear 18, pseudogene

SMIM23 Gene

small integral membrane protein 23

Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM20 Gene

small integral membrane protein 20

Involved in mitochondrial cytochrome c oxidase assembly. Located in mitochondrial inner membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM21 Gene

small integral membrane protein 21

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM24 Gene

small integral membrane protein 24

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

RNU2-1 Gene

RNA, U2 small nuclear 1

The spliceosome is a multicomponent ribonucleoprotein complex that catalyzes the removal of introns from nuclear mRNA precursors. The spliceosome is composed of four small ribonucleoprotein particles (the U1, U2, and U4/U6 snRNPs) and numerous additional proteins. The U2 small nuclear RNA (snRNA) is a RNA component of the U2 snRNP that interacts with the 3' region of the intron at the branch site. Several sites in the human genome express U2 snRNAs. This locus represents an array of U2 snRNA genes located at 17q21-22 that undergoes concerted evolution to homogenize repeat units within the array. Each repeat in this array is approximately 6.1 kb long and contains a single copy of the U2 snRNA. Arrays of six to more than 30 repeats have been reported. [provided by RefSeq, Mar 2009]

RNU7-42P Gene

RNA, U7 small nuclear 42 pseudogene

SNORD32A Gene

small nucleolar RNA, C/D box 32A

Predicted to be involved in RNA processing. Predicted to act upstream of or within glucose metabolic process; insulin secretion; and reactive oxygen species metabolic process. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD32B Gene

small nucleolar RNA, C/D box 32B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-85P Gene

RNA, U7 small nuclear 85 pseudogene

SCLC1 Gene

small cell cancer of the lung

SNORD17 Gene

small nucleolar RNA, C/D box 17

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNHG5 Gene

small nucleolar RNA host gene 5

This gene represent a snoRNA host gene and produces a long non-coding RNA. This RNA may regulate gene expression by acting as a sponge for microRNAs. This transcript may also stabilize mRNAs by blocking degradation by staufen double-stranded RNA binding protein 1. [provided by RefSeq, Dec 2017]

SNHG4 Gene

small nucleolar RNA host gene 4

SNHG7 Gene

small nucleolar RNA host gene 7

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNHG6 Gene

small nucleolar RNA host gene 6

SNHG1 Gene

small nucleolar RNA host gene 1

This locus represents a small nucleolar RNA host gene that produces multiple alternatively spliced long non-coding RNAs. This gene is upregulated in cancers and is thought to act as promoter of cell proliferation. This transcript negatively regulates tumor suppressor genes such as tumor protein p53. Expression of this locus may be a marker of tumor progression. [provided by RefSeq, Dec 2017]

SNHG8 Gene

small nucleolar RNA host gene 8

RNU7-28P Gene

RNA, U7 small nuclear 28 pseudogene

RNU7-65P Gene

RNA, U7 small nuclear 65 pseudogene

RNU7-38P Gene

RNA, U7 small nuclear 38 pseudogene

SNORD15B Gene

small nucleolar RNA, C/D box 15B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD15A Gene

small nucleolar RNA, C/D box 15A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD3B-1 Gene

small nucleolar RNA, C/D box 3B-1

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD3B-2 Gene

small nucleolar RNA, C/D box 3B-2

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

LOC100421673 Gene

small nuclear ribonucleoprotein polypeptide B pseudogene

LOC100421672 Gene

small nuclear ribonucleoprotein polypeptide B pseudogene

LOC101929749 Gene

carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene

TSKU Gene

tsukushi, small leucine rich proteoglycan

Predicted to enable transforming growth factor beta binding activity. Predicted to be involved in several processes, including cholesterol efflux; cholesterol homeostasis; and nervous system development. Predicted to act upstream of or within several processes, including ciliary body morphogenesis; negative regulation of Wnt signaling pathway; and telencephalon development. Predicted to be located in extracellular region. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Mar 2025]

LOC643802 Gene

u3 small nucleolar ribonucleoprotein protein MPP10-like

SNORD83A Gene

small nucleolar RNA, C/D box 83A

Intronic regions of ribosomal protein genes can harbor noncoding small nucleolar RNAs (snoRNAs), like SNORD83A, which are generated during pre-mRNA processing. snoRNAs form part of the small nucleolar ribonucleoprotein particles (snoRNPs) involved in pre-rRNA processing and modification. snoRNAs of the box C/D class, like SNORD83A, function in 2-prime-O-ribose methylation of rRNAs (Duga et al., 2000 [PubMed 10684968]).[supplied by OMIM, Mar 2008]

SNORD83B Gene

small nucleolar RNA, C/D box 83B

Intronic regions of ribosomal protein genes can harbor noncoding small nucleolar RNAs (snoRNAs), like SNORD83B, which are generated during pre-mRNA processing. snoRNAs form part of the small nucleolar ribonucleoprotein particles (snoRNPs) involved in pre-rRNA processing and modification. snoRNAs of the box C/D class, like SNORD83B, function in 2-prime-O-ribose methylation of rRNAs (Duga et al., 2000 [PubMed 10684968]).[supplied by OMIM, Mar 2008]

SNORA71C Gene

small nucleolar RNA, H/ACA box 71C

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA71B Gene

small nucleolar RNA, H/ACA box 71B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA71A Gene

small nucleolar RNA, H/ACA box 71A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA71E Gene

small nucleolar RNA, H/ACA box 71E

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-66P Gene

RNA, U6 small nuclear 66, pseudogene

SNORD85 Gene

small nucleolar RNA, C/D box 85

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

UTP3 Gene

UTP3, small subunit (SSU) processome component, homolog (S. cerevisiae)

Enables RNA binding activity. Involved in ribosomal small subunit biogenesis. Located in nucleolus. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-8P Gene

RNA, U7 small nuclear 8 pseudogene

SNORD114-31 Gene

small nucleolar RNA, C/D box 114-31

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-30 Gene

small nucleolar RNA, C/D box 114-30

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SMKR1 Gene

small lysine-rich protein 1

LOC100820734 Gene

LSM2 homolog, U6 small nuclear RNA associated (S. cerevisiae) pseudogene

RNU7-14P Gene

RNA, U7 small nuclear 14 pseudogene

LOC729200 Gene

small nuclear ribonucleoprotein polypeptide B pseudogene

RNVU1-17 Gene

RNA, variant U1 small nuclear 17

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNVU1-14 Gene

RNA, variant U1 small nuclear 14

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNVU1-15 Gene

RNA, variant U1 small nuclear 15

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNVU1-11 Gene

RNA, variant U1 small nuclear 11

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNVU1-18 Gene

RNA, variant U1 small nuclear 18

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNVU1-19 Gene

RNA, variant U1 small nuclear 19

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

SNORD12 Gene

small nucleolar RNA, C/D box 12

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-30P Gene

RNA, U7 small nuclear 30 pseudogene

SNORD13 Gene

small nucleolar RNA, C/D box 13

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SMIM11P1 Gene

small integral membrane protein 11 pseudogene 1

SNORA68 Gene

small nucleolar RNA, H/ACA box 68

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA64 Gene

small nucleolar RNA, H/ACA box 64

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA65 Gene

small nucleolar RNA, H/ACA box 65

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA66 Gene

small nucleolar RNA, H/ACA box 66

This gene encodes a non-coding RNA that functions in the biogenesis of other small nuclear RNAs. This RNA is found in the nucleolus, where it may be involved in the pseudouridylation of 18S ribosomal RNA. This RNA is found associated with the GAR1 protein. [provided by RefSeq, Apr 2009]

SNORA67 Gene

small nucleolar RNA, H/ACA box 67

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA60 Gene

small nucleolar RNA, H/ACA box 60

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA61 Gene

small nucleolar RNA, H/ACA box 61

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA62 Gene

small nucleolar RNA, H/ACA box 62

Predicted to be involved in RNA processing. Part of box H/ACA RNP complex. [provided by Alliance of Genome Resources, Mar 2025]

SNORA63 Gene

small nucleolar RNA, H/ACA box 63

Predicted to be involved in RNA processing. Part of box H/ACA RNP complex. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116@ Gene

small nucleolar RNA, C/D box 116 cluster

SNAPC5P1 Gene

small nuclear RNA activating complex, polypeptide 5, 19kDa pseudogene 1

SNRPGP13 Gene

small nuclear ribonucleoprotein polypeptide G pseudogene 13

SNRPGP12 Gene

small nuclear ribonucleoprotein polypeptide G pseudogene 12

SNRPGP11 Gene

small nuclear ribonucleoprotein polypeptide G pseudogene 11

SNRPGP14 Gene

small nuclear ribonucleoprotein polypeptide G pseudogene 14

SNORD116-25 Gene

small nucleolar RNA, C/D box 116-25

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-27 Gene

small nucleolar RNA, C/D box 116-27

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-21 Gene

small nucleolar RNA, C/D box 116-21

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU5E-8P Gene

RNA, U5E small nuclear 8, pseudogene

RNU7-51P Gene

RNA, U7 small nuclear 51 pseudogene

SNORD65 Gene

small nucleolar RNA, C/D box 65

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD64 Gene

small nucleolar RNA, C/D box 64

This gene encodes a C/D box-type small nucleolar RNA that is expressed predominantly in the brain. Expression of this RNA is not detectable in the brains of patients with Prader-Willi syndrome. [provided by RefSeq, Jun 2010]

SNORD67 Gene

small nucleolar RNA, C/D box 67

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD66 Gene

small nucleolar RNA, C/D box 66

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD61 Gene

small nucleolar RNA, C/D box 61

Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box C/D class snoRNAs are involved in site-specific 2-prime-O-ribose methylation of preribosomal RNA precursors. This snoRNA is located in an intron of the RNA binding motif protein, X-linked gene (RBMX). [provided by RefSeq, Sep 2009]

SNORD60 Gene

small nucleolar RNA, C/D box 60

Predicted to be involved in RNA processing. Predicted to act upstream of or within intracellular cholesterol transport. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD63 Gene

small nucleolar RNA, C/D box 63

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD69 Gene

small nucleolar RNA, C/D box 69

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD68 Gene

small nucleolar RNA, C/D box 68

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-15P Gene

RNA, U6 small nuclear 15, pseudogene

RNU2-4P Gene

RNA, U2 small nuclear 4, pseudogene

RNU1-15P Gene

RNA, U1 small nuclear 15, pseudogene

RNU5F-4P Gene

RNA, U5F small nuclear 4, pseudogene

RNU6ATAC3P Gene

RNA, U6atac small nuclear 3, pseudogene

SVIP Gene

small VCP/p97-interacting protein

Endoplasmic reticulum-associated degradation (ERAD) is the pathway by which misfolded proteins in the endoplasmic reticulum are targeted to the proteasome for degradation. Multiple specialized proteins interact with one another during ERAD to complete this process. The protein encoded by this gene is an inhibitor of ERAD, functioning to disrupt the interaction of these protein components. This downregulation of ERAD may be needed to protect the cell from overactive protein degradation. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]

SMIM22 Gene

small integral membrane protein 22

Involved in several processes, including lipid droplet formation; positive regulation of cell migration; and regulation of actin cytoskeleton organization. Predicted to be located in late endosome and membrane. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-72P Gene

RNA, U7 small nuclear 72 pseudogene

RNU6-56P Gene

RNA, U6 small nuclear 56, pseudogene

SNORD114-20 Gene

small nucleolar RNA, C/D box 114-20

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNRPGP8 Gene

small nuclear ribonucleoprotein polypeptide G pseudogene 8

SNORD115-21 Gene

small nucleolar RNA, C/D box 115-21

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-20 Gene

small nucleolar RNA, C/D box 115-20

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-23 Gene

small nucleolar RNA, C/D box 115-23

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-22 Gene

small nucleolar RNA, C/D box 115-22

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-25 Gene

small nucleolar RNA, C/D box 115-25

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-24 Gene

small nucleolar RNA, C/D box 115-24

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-27 Gene

small nucleolar RNA, C/D box 115-27

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-26 Gene

small nucleolar RNA, C/D box 115-26

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-29 Gene

small nucleolar RNA, C/D box 115-29

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-28 Gene

small nucleolar RNA, C/D box 115-28

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

LOC100131448 Gene

CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2 pseudogene

RNU3P2 Gene

RNA, U3 small nucleolar pseudogene 2

RNU3P3 Gene

RNA, U3 small nucleolar pseudogene 3

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU3P1 Gene

RNA, U3 small nucleolar pseudogene 1

RNU3P4 Gene

RNA, U3 small nucleolar pseudogene 4

SNHG15 Gene

small nucleolar RNA host gene 15

This gene represents a snoRNA host gene that produces a short-lived long non-coding RNA. This non-coding RNA is upregulated in tumor cells and may contribute to cell proliferation by acting as a sponge for microRNAs. [provided by RefSeq, Dec 2017]

SNHG14 Gene

small nucleolar RNA host gene 14

This gene is located within the Prader-Willi critical region and produces a long, spliced paternally-imprinted RNA that initiates within a common upstream promoter region shared by the SNRPN (small nuclear ribonucleoprotein polypeptide N) and SNURF genes. This transcript serves as a host RNA for the small nucleolar RNA, C/D box 115 and 116 clusters. This RNA extends in antisense into the region of the ubiquitin protein ligase E3A gene (UBE3A), and is thought to regulate imprinted expression of UBE3A in the brain. This transcript undergoes extensive alternative splicing, and may initiate and terminate at multiple locations within this genomic region. The full-length structure of all splice forms is not determined. [provided by RefSeq, Mar 2017]

SNHG17 Gene

small nucleolar RNA host gene 17

SNHG16 Gene

small nucleolar RNA host gene 16

SNHG11 Gene

small nucleolar RNA host gene 11

This gene is a member of the non-protein-coding multiple snoRNA host gene family. Two snoRNAs are derived from the introns of this host gene. Although many alternative splice variants have been observed, the gene is thought to have no protein-coding potential. [provided by RefSeq, Jul 2008]

SNHG12 Gene

small nucleolar RNA host gene 12

This gene produces a long RNA that is overexpressed in tumor cells. This RNA may promote tumorigenesis by acting as a sponge for microRNAs. [provided by RefSeq, Dec 2017]

SNHG19 Gene

small nucleolar RNA host gene 19

SNHG18 Gene

small nucleolar RNA host gene 18

SNORA80E Gene

small nucleolar RNA, H/ACA box 80E

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA80B Gene

small nucleolar RNA, H/ACA box 80B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA80A Gene

small nucleolar RNA, H/ACA box 80A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU4-9P Gene

RNA, U4 small nuclear 9, pseudogene

RNU6-71P Gene

RNA, U6 small nuclear 71, pseudogene

SNORA45A Gene

small nucleolar RNA, H/ACA box 45A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-22P Gene

RNA, U7 small nuclear 22 pseudogene

SNRPB2 Gene

small nuclear ribonucleoprotein polypeptide B

The protein encoded by this gene associates with stem loop IV of U2 small nuclear ribonucleoprotein (U2 snRNP) in the presence of snRNP-A'. The encoded protein may play a role in pre-mRNA splicing. Autoantibodies from patients with systemic lupus erythematosus frequently recognize epitopes on the encoded protein. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]

ASH2LP1 Gene

ash2 (absent, small, or homeotic)-like (Drosophila) pseudogene 1

RNU7-59P Gene

RNA, U7 small nuclear 59 pseudogene

SNORD88A Gene

small nucleolar RNA, C/D box 88A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD88B Gene

small nucleolar RNA, C/D box 88B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD88C Gene

small nucleolar RNA, C/D box 88C

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-26P Gene

RNA, U6 small nuclear 26, pseudogene

UTP11L Gene

UTP11-like, U3 small nucleolar ribonucleoprotein (yeast)

Enables RNA binding activity. Involved in nervous system development; positive regulation of apoptotic process; and ribosomal small subunit biogenesis. Located in cytoplasm; extracellular space; and nucleolus. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-10P Gene

RNA, U6 small nuclear 10, pseudogene

SNORD114-1 Gene

small nucleolar RNA, C/D box 114-1

Small nucleolar RNAs (snoRNAs), like SNORD114-1, guide the formation of 2-prime O-methylation of ribosomal RNA (rRNA) and U small nuclear RNAs (snRNAs) through a specific RNA duplex at each modification site. SNORD114-1 is 1 of 31 tandem SNORD114 genes on chromosome 14q32 (Cavaille et al., 2002 [PubMed 12045206]).[supplied by OMIM, Nov 2010]

SNORD114-6 Gene

small nucleolar RNA, C/D box 114-6

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-5 Gene

small nucleolar RNA, C/D box 114-5

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-4 Gene

small nucleolar RNA, C/D box 114-4

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

ASH1L Gene

ash1 (absent, small, or homeotic)-like (Drosophila)

This gene encodes a member of the trithorax group of transcriptional activators. The protein contains four AT hooks, a SET domain, a PHD-finger motif, and a bromodomain. It is localized to many small speckles in the nucleus, and also to cell-cell tight junctions. [provided by RefSeq, Jul 2008]

LOC100422490 Gene

UTP6, small subunit (SSU) processome component, homolog (yeast) pseudogene

LOC100422497 Gene

UTP18, small subunit (SSU) processome component, homolog (yeast) pseudogene

RNU7-41P Gene

RNA, U7 small nuclear 41 pseudogene

SCARNA27 Gene

small Cajal body-specific RNA 27

SCARNA22 Gene

small Cajal body-specific RNA 22

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA23 Gene

small Cajal body-specific RNA 23

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA20 Gene

small Cajal body-specific RNA 20

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA21 Gene

small Cajal body-specific RNA 21

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU6ATAC4P Gene

RNA, U6atac small nuclear 4, pseudogene

RNU1-3 Gene

RNA, U1 small nuclear 3

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNU1-2 Gene

RNA, U1 small nuclear 2

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-31P Gene

RNA, U6 small nuclear 31, pseudogene

SNORD115-5 Gene

small nucleolar RNA, C/D box 115-5

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-2 Gene

small nucleolar RNA, C/D box 115-2

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-3 Gene

small nucleolar RNA, C/D box 115-3

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-8 Gene

small nucleolar RNA, C/D box 115-8

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-9 Gene

small nucleolar RNA, C/D box 115-9

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD101 Gene

small nucleolar RNA, C/D box 101

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD100 Gene

small nucleolar RNA, C/D box 100

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD102 Gene

small nucleolar RNA, C/D box 102

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD105 Gene

small nucleolar RNA, C/D box 105

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD104 Gene

small nucleolar RNA, C/D box 104

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD107 Gene

small nucleolar RNA, C/D box 107

Small nucleolar RNAs (snoRNAs) are small non-coding RNAs involved in RNA processing. Box C/D class snoRNAs are involved in site-specific 2-prime-O-ribose methylation of preribosomal RNA precursors. This snoRNA is located in a cluster of genes including the SNURF-SNRPN gene, which serves as a host for multiple snoRNAs. [provided by RefSeq, Oct 2011]

SNORD108 Gene

small nucleolar RNA, C/D box 108

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-60P Gene

RNA, U7 small nuclear 60 pseudogene

LOC441722 Gene

U2 small nuclear RNA auxiliary factor 1-like 4 pseudogene

SNORD23 Gene

small nucleolar RNA, C/D box 23

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNAR-B2 Gene

small ILF3/NF90-associated RNA B2

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SNAR-B1 Gene

small ILF3/NF90-associated RNA B1

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

RNU5B-3P Gene

RNA, U5B small nuclear 3, pseudogene

LOC100631374 Gene

M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene

SNRNP40 Gene

small nuclear ribonucleoprotein 40kDa (U5)

This gene encodes a component of the U5 small nuclear ribonucleoprotein (snRNP) particle. The U5 snRNP is part of the spliceosome, a multiprotein complex that catalyzes the removal of introns from pre-messenger RNAs. [provided by RefSeq, Jul 2008]

SNRNP48 Gene

small nuclear ribonucleoprotein 48kDa (U11/U12)

Predicted to enable metal ion binding activity. Predicted to be involved in RNA splicing. Located in cytosol and nucleoplasm. Part of U12-type spliceosomal complex. [provided by Alliance of Genome Resources, Mar 2025]

CDC42SE2 Gene

CDC42 small effector 2

Enables signaling adaptor activity. Involved in regulation of signal transduction. Located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025]

CDC42SE1 Gene

CDC42 small effector 1

Predicted to enable GTPase inhibitor activity. Predicted to be involved in signal transduction. Located in cell junction. [provided by Alliance of Genome Resources, Mar 2025]

RNU1-22P Gene

RNA, U1 small nuclear 22, pseudogene

SCARNA5 Gene

small Cajal body-specific RNA 5

Predicted to be involved in RNA processing. Located in Cajal body. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA4 Gene

small Cajal body-specific RNA 4

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SMAGP Gene

small cell adhesion glycoprotein

Located in cell junction; nucleoplasm; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025]

RN7SKP8 Gene

RNA, 7SK small nuclear pseudogene 8

RN7SKP9 Gene

RNA, 7SK small nuclear pseudogene 9

RN7SKP6 Gene

RNA, 7SK small nuclear pseudogene 6

RN7SKP7 Gene

RNA, 7SK small nuclear pseudogene 7

RN7SKP4 Gene

RNA, 7SK small nuclear pseudogene 4

RN7SKP5 Gene

RNA, 7SK small nuclear pseudogene 5

RN7SKP2 Gene

RNA, 7SK small nuclear pseudogene 2

RN7SKP3 Gene

RNA, 7SK small nuclear pseudogene 3

SCARNA2 Gene

small Cajal body-specific RNA 2

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNHG3 Gene

small nucleolar RNA host gene 3

Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SMIM2 Gene

small integral membrane protein 2

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM1 Gene

small integral membrane protein 1 (Vel blood group)

This gene encodes a small, conserved protein that participates in red blood cell formation. The encoded protein is localized to the cell membrane and is the antigen for the Vel blood group. Alternative splicing results in different transcript variants that encode the same protein. [provided by RefSeq, Dec 2013]

SNHG9 Gene

small nucleolar RNA host gene 9

RNU7-80P Gene

RNA, U7 small nuclear 80 pseudogene

RNU7-11P Gene

RNA, U7 small nuclear 11 pseudogene

LOC643605 Gene

CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2 pseudogene

RNU7-35P Gene

RNA, U7 small nuclear 35 pseudogene

SNORD45C Gene

small nucleolar RNA, C/D box 45C

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD45B Gene

small nucleolar RNA, C/D box 45B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-68P Gene

RNA, U7 small nuclear 68 pseudogene

SNORD18A Gene

small nucleolar RNA, C/D box 18A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD18C Gene

small nucleolar RNA, C/D box 18C

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD18B Gene

small nucleolar RNA, C/D box 18B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA53 Gene

small nucleolar RNA, H/ACA box 53

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SMIM10L1 Gene

small integral membrane protein 10 like 1

Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025]

SNORA76C Gene

small nucleolar RNA, H/ACA box 76C

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA76A Gene

small nucleolar RNA, H/ACA box 76A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-52P Gene

RNA, U7 small nuclear 52 pseudogene

RNU5A-4P Gene

RNA, U5A small nuclear 4, pseudogene

SNORD3D Gene

small nucleolar RNA, C/D box 3D

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD3@ Gene

small nucleolar RNA, C/D box 3 cluster

SNORD3A Gene

small nucleolar RNA, C/D box 3A

U3 RNA, an abundant small nucleolar RNA (snoRNA), is thought to play a role in the processing of ribosomal RNA precursors (Bernstein et al., 1983 [PubMed 6186397]).[supplied by OMIM, Jun 2009]

SNORD37 Gene

small nucleolar RNA, C/D box 37

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD34 Gene

small nucleolar RNA, C/D box 34

Predicted to be involved in RNA processing. Predicted to act upstream of or within glucose metabolic process; insulin secretion; and reactive oxygen species metabolic process. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD33 Gene

small nucleolar RNA, C/D box 33

Predicted to be involved in RNA processing. Predicted to act upstream of or within glucose metabolic process; insulin secretion; and reactive oxygen species metabolic process. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD30 Gene

small nucleolar RNA, C/D box 30

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD31 Gene

small nucleolar RNA, C/D box 31

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-45P Gene

RNA, U6 small nuclear 45, pseudogene

RNU6-34P Gene

RNA, U6 small nuclear 34, pseudogene

LSM1P1 Gene

LSM1, U6 small nuclear RNA associated pseudogene 1

LOC102724677 Gene

carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene

RNU6-55P Gene

RNA, U6 small nuclear 55, pseudogene

SNORA19 Gene

small nucleolar RNA, H/ACA box 19

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA18 Gene

small nucleolar RNA, H/ACA box 18

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA15 Gene

small nucleolar RNA, H/ACA box 15

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA17 Gene

small nucleolar RNA, H/ACA box 17

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA12 Gene

small nucleolar RNA, H/ACA box 12

Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA12, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]

RNU5F-7P Gene

RNA, U5F small nuclear 7, pseudogene

Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-19P Gene

RNA, U7 small nuclear 19 pseudogene

RNU7-78P Gene

RNA, U7 small nuclear 78 pseudogene

RNU4ATAC Gene

RNA, U4atac small nuclear (U12-dependent splicing)

The small nuclear RNA (snRNA) encoded by this gene is part of the U12-dependent minor spliceosome complex. In addition to the encoded RNA, this ribonucleoprotein complex consists of U11, U12, U5, and U6atac snRNAs. The U12-dependent spliceosome acts on approximately 700 specific introns in the human genome. Defects in this gene are a cause of microcephalic osteodysplastic primordial dwarfism type 1 (MOPD). [provided by RefSeq, Jul 2011]

RNU7-25P Gene

RNA, U7 small nuclear 25 pseudogene

RNU7-81P Gene

RNA, U7 small nuclear 81 pseudogene

SNAR-C3 Gene

small ILF3/NF90-associated RNA C3

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-23P Gene

RNA, U6 small nuclear 23, pseudogene

RNU7-10P Gene

RNA, U7 small nuclear 10 pseudogene

CTDSP1 Gene

CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase 1

This gene encodes a member of the small C-terminal domain phosphatase (SCP) family of nuclear phosphatases. These proteins play a role in transcriptional regulation through specific dephosphorylation of phosphoserine 5 within tandem heptapeptide repeats of the C-terminal domain of RNA polymerase II. The encoded protein plays a role in neuronal gene silencing in non-neuronal cells, and may also inhibit osteoblast differentiation. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011]

CTDSP2 Gene

CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase 2

Enables RNA polymerase II CTD heptapeptide repeat phosphatase activity. Involved in protein dephosphorylation. Predicted to be located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025]

CTDSPL Gene

CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase-like

Predicted to enable RNA polymerase II CTD heptapeptide repeat phosphatase activity. Predicted to be involved in chromatin remodeling and regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of G1/S transition of mitotic cell cycle and negative regulation of protein phosphorylation. Located in extracellular exosome. Biomarker of lung non-small cell carcinoma. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-20P Gene

RNA, U7 small nuclear 20 pseudogene

SNORD116-10 Gene

small nucleolar RNA, C/D box 116-10

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-12 Gene

small nucleolar RNA, C/D box 116-12

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-6P Gene

RNA, U7 small nuclear 6 pseudogene

RNU7-77P Gene

RNA, U7 small nuclear 77 pseudogene

RN7SK Gene

RNA, 7SK small nuclear

Predicted to be involved in negative regulation of transcription elongation by RNA polymerase II. Part of 7SK snRNP. [provided by Alliance of Genome Resources, Mar 2025]

UTP18 Gene

UTP18 small subunit (SSU) processome component homolog (yeast)

Enables RNA binding activity. Involved in ribosomal small subunit biogenesis. Located in nuclear membrane; nucleolus; and nucleoplasm. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025]

SNORA36A Gene

small nucleolar RNA, H/ACA box 36A

Biosynthesis of stable cellular RNAs such as tRNAs, rRNAs, snRNAs, and snoRNAs is aided by covalent nucleotide modification after transcription. The modified nucleotides are involved in correct RNA folding, establishment of correct RNA-RNA and RNA-protein interactions, and in the correct function of mature RNAs. The RNA encoded by this gene is thought to mediate the pseudouridylation of residues U105 and U1244 of 18S rRNA. [provided by RefSeq, Feb 2009]

SNAR-A14 Gene

small ILF3/NF90-associated RNA A14

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SNAR-A11 Gene

small ILF3/NF90-associated RNA A11

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SNAR-A10 Gene

small ILF3/NF90-associated RNA A10

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD3C Gene

small nucleolar RNA, C/D box 3C

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD105B Gene

small nucleolar RNA, C/D box 105B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU5D-1 Gene

RNA, U5D small nuclear 1

Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U5 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNU4-6P Gene

RNA, U4 small nuclear 6, pseudogene

SNORA71D Gene

small nucleolar RNA, H/ACA box 71D

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

LOC100303749 Gene

LSM3 homolog, U6 small nuclear RNA associated (S. cerevisiae) pseudogene

SNAR-A3 Gene

small ILF3/NF90-associated RNA A3

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SNAR-A2 Gene

small ILF3/NF90-associated RNA A2

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SNAR-A7 Gene

small ILF3/NF90-associated RNA A7

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SNAR-A6 Gene

small ILF3/NF90-associated RNA A6

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SNAR-A5 Gene

small ILF3/NF90-associated RNA A5

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SNAR-A4 Gene

small ILF3/NF90-associated RNA A4

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA16A Gene

small nucleolar RNA, H/ACA box 16A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

CMSS1 Gene

cms1 ribosomal small subunit homolog (yeast)

Enables RNA binding activity. [provided by Alliance of Genome Resources, Mar 2025]

SNRNP70 Gene

small nuclear ribonucleoprotein 70kDa (U1)

Enables U1 snRNA binding activity. Involved in mRNA splicing, via spliceosome and regulation of RNA splicing. Located in nucleoplasm. Part of U1 snRNP and spliceosomal complex. Implicated in disease of mental health and systemic lupus erythematosus. Biomarker of Alzheimer's disease. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-49P Gene

RNA, U7 small nuclear 49 pseudogene

RNU5E-1 Gene

RNA, U5E small nuclear 1

Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U5 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

SNORD70 Gene

small nucleolar RNA, C/D box 70

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU1-21P Gene

RNA, U1 small nuclear 21, pseudogene

LOC100421863 Gene

ash2 (absent, small, or homeotic)-like (Drosophila) pseudogene

RNU7-44P Gene

RNA, U7 small nuclear 44 pseudogene

SNORD116-5 Gene

small nucleolar RNA, C/D box 116-5

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-7 Gene

small nucleolar RNA, C/D box 116-7

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-87P Gene

RNA, U7 small nuclear 87 pseudogene

RNU7-12P Gene

RNA, U7 small nuclear 12 pseudogene

RNU6ATAC Gene

RNA, U6atac small nuclear (U12-dependent splicing)

Predicted to enable U4atac snRNA binding activity and pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition and spliceosomal tri-snRNP complex assembly. Predicted to be part of U6atac snRNP. [provided by Alliance of Genome Resources, Mar 2025]

SNORD62B Gene

small nucleolar RNA, C/D box 62B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SMIM12P1 Gene

small integral membrane protein 12 pseudogene 1

SPTSSA Gene

serine palmitoyltransferase, small subunit A

Serine palmitoyltransferase (SPT; EC 2.3.1.50) catalyzes the first committed and rate-limiting step in sphingolipid biosynthesis. SSSPTA is a small SPT subunit that stimulates SPT activity and confers acyl-CoA preference to the SPT catalytic heterodimer of SPTLC1 (MIM 605712) and either SPTLC2 (MIM 605713) or SPTLC3 (MIM 611120) (Han et al., 2009 [PubMed 19416851]).[supplied by OMIM, Nov 2010]

SPTSSB Gene

serine palmitoyltransferase, small subunit B

Serine palmitoyltransferase (SPT; EC 2.3.1.50) catalyzes the first committed and rate-limiting step in sphingolipid biosynthesis. SSSPTB is a small SPT subunit that stimulates SPT activity and confers acyl-CoA preference to the SPT catalytic heterodimer of SPTLC1 (MIM 605712) and either SPTLC2 (MIM 605713) or SPTLC3 (MIM 611120) (Han et al., 2009 [PubMed 19416851]).[supplied by OMIM, Nov 2010]

SNORA11 Gene

small nucleolar RNA, H/ACA box 11

Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA11, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]

SNORA10 Gene

small nucleolar RNA, H/ACA box 10

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA13 Gene

small nucleolar RNA, H/ACA box 13

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

LOC102724822 Gene

carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene

UTP6 Gene

UTP6, small subunit (SSU) processome component, homolog (yeast)

Predicted to enable snoRNA binding activity. Involved in ribosomal small subunit biogenesis. Located in chromosome and nucleolus. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025]

SNORD126 Gene

small nucleolar RNA, C/D box 126

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD125 Gene

small nucleolar RNA, C/D box 125

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

LOC105377886 Gene

small EDRK-rich factor 2 pseudogene

RSG1 Gene

REM2 and RAB-like small GTPase 1

Predicted to enable GTP binding activity. Predicted to be involved in cilium assembly; protein localization; and regulation of vesicle-mediated transport. Predicted to act upstream of or within several processes, including axoneme assembly; endocardial cushion fusion; and regulation of smoothened signaling pathway. Located in centriole; ciliary basal body; and ciliary transition zone. [provided by Alliance of Genome Resources, Mar 2025]

RNU5B-6P Gene

RNA, U5B small nuclear 6, pseudogene

SNORA73A Gene

small nucleolar RNA, H/ACA box 73A

Predicted to be involved in RNA processing. Located in nucleus. Part of box H/ACA RNP complex. [provided by Alliance of Genome Resources, Mar 2025]

SNORA73B Gene

small nucleolar RNA, H/ACA box 73B

RNU7-57P Gene

RNA, U7 small nuclear 57 pseudogene

RNU6-52P Gene

RNA, U6 small nuclear 52, pseudogene

RAC2 Gene

ras-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2)

This gene encodes a member of the Ras superfamily of small guanosine triphosphate (GTP)-metabolizing proteins. The encoded protein localizes to the plasma membrane, where it regulates diverse processes, such as secretion, phagocytosis, and cell polarization. Activity of this protein is also involved in the generation of reactive oxygen species. Mutations in this gene are associated with neutrophil immunodeficiency syndrome. There is a pseudogene for this gene on chromosome 6. [provided by RefSeq, Jul 2013]

RAC3 Gene

ras-related C3 botulinum toxin substrate 3 (rho family, small GTP binding protein Rac3)

The protein encoded by this gene is a GTPase which belongs to the RAS superfamily of small GTP-binding proteins. Members of this superfamily appear to regulate a diverse array of cellular events, including the control of cell growth, cytoskeletal reorganization, and the activation of protein kinases. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2015]

RAC1 Gene

ras-related C3 botulinum toxin substrate 1 (rho family, small GTP binding protein Rac1)

The protein encoded by this gene is a GTPase which belongs to the RAS superfamily of small GTP-binding proteins. Members of this superfamily appear to regulate a diverse array of cellular events, including the control of cell growth, cytoskeletal reorganization, and the activation of protein kinases. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]

SNAR-A12 Gene

small ILF3/NF90-associated RNA A12

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-88P Gene

RNA, U7 small nuclear 88 pseudogene

RN7SKP10 Gene

RNA, 7SK small nuclear pseudogene 10

BA395L14.12 Gene

small nuclear ribonucleoprotein polypeptide A' pseudogene

RNU6-58P Gene

RNA, U6 small nuclear 58, pseudogene

RNU5E-9P Gene

RNA, U5E small nuclear 9, pseudogene

SNORD113-1 Gene

small nucleolar RNA, C/D box 113-1

Small nucleolar RNAs (snoRNAs), like SNORD113-1, guide the formation of 2-prime O-methylation of ribosomal RNA (rRNA) and U small nuclear RNAs (snRNAs) through a specific RNA duplex at each modification site. SNORD113-1 is 1 of 9 tandem SNORD113 genes on chromosome 14q32 (Cavaille et al., 2002 [PubMed 12045206]).[supplied by OMIM, Nov 2010]

SNORD113-3 Gene

small nucleolar RNA, C/D box 113-3

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-42 Gene

small nucleolar RNA, C/D box 115-42

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-40 Gene

small nucleolar RNA, C/D box 115-40

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-46 Gene

small nucleolar RNA, C/D box 115-46

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-45 Gene

small nucleolar RNA, C/D box 115-45

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-44 Gene

small nucleolar RNA, C/D box 115-44

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-48 Gene

small nucleolar RNA, C/D box 115-48

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD42B Gene

small nucleolar RNA, C/D box 42B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD42A Gene

small nucleolar RNA, C/D box 42A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA46 Gene

small nucleolar RNA, H/ACA box 46

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA47 Gene

small nucleolar RNA, H/ACA box 47

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA44 Gene

small nucleolar RNA, H/ACA box 44

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA43 Gene

small nucleolar RNA, H/ACA box 43

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA40 Gene

small nucleolar RNA, H/ACA box 40

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA41 Gene

small nucleolar RNA, H/ACA box 41

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA48 Gene

small nucleolar RNA, H/ACA box 48

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA49 Gene

small nucleolar RNA, H/ACA box 49

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114@ Gene

small nucleolar RNA, C/D box 114 cluster

RNU7-73P Gene

RNA, U7 small nuclear 73 pseudogene

RNU6V Gene

RNA, U6 small nuclear variant sequence with SNRPE pseudogene sequence

SNORD58A Gene

small nucleolar RNA, C/D box 58A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD58C Gene

small nucleolar RNA, C/D box 58C

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD58B Gene

small nucleolar RNA, C/D box 58B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD89 Gene

small nucleolar RNA, C/D box 89

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD87 Gene

small nucleolar RNA, C/D box 87

Small nucleolar RNAs (snoRNAs) of the C/D class, such as SNORD87, are involved in 2-prime-methylation of preribosomal RNA precursors (Gogolevskaya et al., 2002 [PubMed 12119114]).[supplied by OMIM, Aug 2008]

SNORD86 Gene

small nucleolar RNA, C/D box 86

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD84 Gene

small nucleolar RNA, C/D box 84

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD82 Gene

small nucleolar RNA, C/D box 82

The majority of small nucleolar RNAs (snoRNAs) function as guide RNAs in the nucleotide modification of preribosomal RNA (pre-rRNA). C/D box snoRNAs, like SNORD82, are involved in site-specific 2-prime-O-ribose methylation of pre-rRNA (Rebane and Metspalu, 1999 [PubMed 10524220]).[supplied by OMIM, Mar 2008]

SNORD81 Gene

small nucleolar RNA, C/D box 81

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD80 Gene

small nucleolar RNA, C/D box 80

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU5E-5P Gene

RNA, U5E small nuclear 5, pseudogene

SGTB Gene

small glutamine-rich tetratricopeptide repeat (TPR)-containing, beta

Predicted to enable molecular adaptor activity. Predicted to be involved in post-translational protein targeting to endoplasmic reticulum membrane. Predicted to be part of TRC complex. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SGTA Gene

small glutamine-rich tetratricopeptide repeat (TPR)-containing, alpha

This gene encodes a protein which is capable of interacting with the major nonstructural protein of parvovirus H-1 and 70-kDa heat shock cognate protein; however, its function is not known. Since this transcript is expressed ubiquitously in various tissues, this protein may serve a housekeeping function. [provided by RefSeq, Jul 2008]

SNRPGP10 Gene

small nuclear ribonucleoprotein polypeptide G pseudogene 10

SNRPGP15 Gene

small nuclear ribonucleoprotein polypeptide G pseudogene 15

Predicted to contribute to RNA binding activity. Predicted to be involved in mRNA splicing, via spliceosome. Predicted to be located in nucleus. Predicted to be part of SMN-Sm protein complex and nucleus. Predicted to be active in P granule. [provided by Alliance of Genome Resources, Mar 2025]

RNU1-17P Gene

RNA, U1 small nuclear 17, pseudogene

RNU2-2P Gene

RNA, U2 small nuclear 2, pseudogene

RNU5F-2P Gene

RNA, U5F small nuclear 2, pseudogene

RNU7-74P Gene

RNA, U7 small nuclear 74 pseudogene

RNU6-50P Gene

RNA, U6 small nuclear 50, pseudogene

SMIM3 Gene

small integral membrane protein 3

Enables identical protein binding activity. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM7 Gene

small integral membrane protein 7

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM6 Gene

small integral membrane protein 6

Predicted to act upstream of or within negative regulation of ATPase-coupled calcium transmembrane transporter activity. Predicted to be located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM5 Gene

small integral membrane protein 5

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM4 Gene

small integral membrane protein 4

Enables mitochondrial ribosome binding activity. Involved in mitochondrial cytochrome c oxidase assembly. Located in mitochondrion. Is active in mitochondrial inner membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM9 Gene

small integral membrane protein 9

Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM8 Gene

small integral membrane protein 8

Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-36 Gene

small nucleolar RNA, C/D box 115-36

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-37 Gene

small nucleolar RNA, C/D box 115-37

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-33 Gene

small nucleolar RNA, C/D box 115-33

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-30 Gene

small nucleolar RNA, C/D box 115-30

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-31 Gene

small nucleolar RNA, C/D box 115-31

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU5E-2P Gene

RNA, U5E small nuclear 2, pseudogene

SNORD50A Gene

small nucleolar RNA, C/D box 50A

SNORD50A belongs to the C/D box class of small nucleolar RNAs (snoRNAs), which are thought to function as guide RNAs in the site-specific ribose methylation of preribosomal RNA (Kiss-Laszlo et al., 1996 [PubMed 8674114]).[supplied by OMIM, Nov 2009]

SNORD50B Gene

small nucleolar RNA, C/D box 50B

SNORD50B is a C/D box-type small nucleolar RNA (snoRNA) that is predicted to function as a guide RNA in 2-prime O-methylation of 28S ribosomal RNA (Tanaka et al., 2000 [PubMed 10792466]).[supplied by OMIM, Feb 2010]

SNORA16B Gene

small nucleolar RNA, H/ACA box 16B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNRNP25 Gene

small nuclear ribonucleoprotein 25kDa (U11/U12)

Two types of spliceosomes catalyze splicing of pre-mRNAs. The major U2-type spliceosome is found in all eukaryotes and removes U2-type introns, which represent more than 99% of pre-mRNA introns. The minor U12-type spliceosome is found in some eukaryotes and removes U12-type introns, which are rare and have distinct splice consensus signals. The U12-type spliceosome consists of several small nuclear RNAs and associated proteins. This gene encodes a 25K protein that is a component of the U12-type spliceosome. [provided by RefSeq, Apr 2010]

SNRNP27 Gene

small nuclear ribonucleoprotein 27kDa (U4/U6.U5)

This gene encodes a serine/arginine-rich (SR) protein. SR proteins play important roles in pre-mRNA splicing by facilitating the recognition and selection of splice sites. The encoded protein associates with the 25S U4/U6.U5 tri-snRNP, a major component of the U2-type spiceosome. The expression of this gene may be altered in cells infected with the human T-cell lymphotropic virus type 1 (HTLV-1) retrovirus. A pseudogene of this gene is located on the long arm of chromosome 5. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Feb 2011]

RNU6-82P Gene

RNA, U6 small nuclear 82, pseudogene

RNU1-24P Gene

RNA, U1 small nuclear 24, pseudogene

RNU7-43P Gene

RNA, U7 small nuclear 43 pseudogene

SNORA11E Gene

small nucleolar RNA, H/ACA box 11E

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SPRR1A Gene

small proline-rich protein 1A

A structural constituent of skin epidermis. Involved in keratinocyte differentiation and peptide cross-linking. Located in cornified envelope. [provided by Alliance of Genome Resources, Mar 2025]

SPRR1B Gene

small proline-rich protein 1B

The protein encoded by this gene is an envelope protein of keratinocytes. The encoded protein is crosslinked to membrane proteins by transglutaminase, forming an insoluble layer under the plasma membrane. This protein is proline-rich and contains several tandem amino acid repeats. [provided by RefSeq, Nov 2015]

SERF1A Gene

small EDRK-rich factor 1A (telomeric)

This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The duplication region includes both a telomeric and a centromeric copy of this gene. Deletions of this gene, the telomeric copy, often accompany deletions of the neighboring SMN1 gene in spinal muscular atrophy (SMA) patients, and so it is thought that this gene may be a modifier of the SMA phenotype. The function of this protein is not known; however, it bears low-level homology with the RNA-binding domain of matrin-cyclophilin, a protein which colocalizes with small nuclear ribonucleoproteins (snRNPs) and the SMN1 gene product. Alternatively spliced transcripts have been documented but it is unclear whether alternative splicing occurs for both the centromeric and telomeric copies of the gene. [provided by RefSeq, Jul 2008]

SERF1B Gene

small EDRK-rich factor 1B (centromeric)

This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This gene is the centromeric copy which is identical to the telomeric copy. Alternatively spliced transcripts have been documented but it is unclear whether alternative splicing occurs for both the centromeric and telomeric copies of the gene. The gene encodes a protein of unknown function which bears low-level homology with the RNA-binding domain of matrin-cyclophilin, a protein which colocalizes with small nuclear ribonucleoproteins (snRNPs) and the SMN1 gene product. [provided by RefSeq, Jul 2008]

RNU7-66P Gene

RNA, U7 small nuclear 66 pseudogene

RNU6-19P Gene

RNA, U6 small nuclear 19, pseudogene

LOC100736412 Gene

ash2 (absent, small, or homeotic)-like (Drosophila) pseudogene

SNORA69 Gene

small nucleolar RNA, H/ACA box 69

This gene encodes a member of the family of box ACA small nucleolar RNAs, characterized by a consensus ACA motif positioned 3 nucleotides from the 3' end of the RNAs and a double-hairpin structure. The box ACA small nucleolar RNAs may play a role in rRNA maturation. This gene is co-transcribed with the ribosomal protein L39 gene. [provided by RefSeq, Oct 2009]

RNU4-3P Gene

RNA, U4 small nuclear 3, pseudogene

RNU6-16P Gene

RNA, U6 small nuclear 16, pseudogene

IMP3 Gene

IMP3, U3 small nucleolar ribonucleoprotein

This gene encodes the human homolog of the yeast Imp3 protein. The protein localizes to the nucleoli and interacts with the U3 snoRNP complex. The protein contains an S4 domain. [provided by RefSeq, Jul 2008]

IMP4 Gene

IMP4, U3 small nucleolar ribonucleoprotein

The protein encoded by this gene, along with IMP3 and MPP10, is part of the 60-80S U3 small nucleolar ribonucleoprotein (U3 snoRNP) complex. This complex is necessary for the early cleavage steps of pre-18S ribosomal RNA processing. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]

SNORA70B Gene

small nucleolar RNA, H/ACA box 70B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA70D Gene

small nucleolar RNA, H/ACA box 70D

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA70E Gene

small nucleolar RNA, H/ACA box 70E

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA70F Gene

small nucleolar RNA, H/ACA box 70F

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA70G Gene

small nucleolar RNA, H/ACA box 70G

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-9P Gene

RNA, U7 small nuclear 9 pseudogene

RNU7-82P Gene

RNA, U7 small nuclear 82 pseudogene

RNU7-17P Gene

RNA, U7 small nuclear 17 pseudogene

RNU105B Gene

RNA, U105B small nucleolar

Predicted to be involved in RNA processing. Predicted to act upstream of or within response to bacterium. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

LOC401703 Gene

U2 small nuclear RNA auxiliary factor 1-like 4 pseudogene

RNU6-6P Gene

RNA, U6 small nuclear 6, pseudogene

Predicted to be located in nuclear speck. [provided by Alliance of Genome Resources, Mar 2025]

SMIM10L2B Gene

small integral membrane protein 10 like 2B

RNVU1-20 Gene

RNA, variant U1 small nuclear 20

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

LOC100736411 Gene

ash2 (absent, small, or homeotic)-like (Drosophila) pseudogene

RNU4-1 Gene

RNA, U4 small nuclear 1

Predicted to enable U6 snRNA binding activity. Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4 snRNP and U4/U6 x U5 tri-snRNP complex. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-37P Gene

RNA, U7 small nuclear 37 pseudogene

SNORA7B Gene

small nucleolar RNA, H/ACA box 7B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA7A Gene

small nucleolar RNA, H/ACA box 7A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA79 Gene

small nucleolar RNA, H/ACA box 79

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA78 Gene

small nucleolar RNA, H/ACA box 78

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA77 Gene

small nucleolar RNA, H/ACA box 77

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA75 Gene

small nucleolar RNA, H/ACA box 75

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA72 Gene

small nucleolar RNA, H/ACA box 72

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA70 Gene

small nucleolar RNA, H/ACA box 70

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD49B Gene

small nucleolar RNA, C/D box 49B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

LOC100130001 Gene

small nuclear ribonucleoprotein polypeptide B pseudogene

SNORD116-30 Gene

small nucleolar RNA, C/D box 116-30

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-18P Gene

RNA, U7 small nuclear 18 pseudogene

RNU86 Gene

RNA, U86 small nucleolar

Intronic regions of ribosomal protein genes can harbor noncoding small nucleolar RNAs (snoRNAs), like U86, which are generated during pre-mRNA processing. snoRNAs form part of the small nucleolar ribonucleoprotein particles (snoRNPs) involved in pre-rRNA processing and modification. snoRNAs of the box C/D class, like U86, function in 2-prime-O-ribose methylation of rRNAs (Duga et al., 2000 [PubMed 10684968]).[supplied by OMIM, Mar 2008]

HSPB11 Gene

heat shock protein family B (small), member 11

Predicted to enable metal ion binding activity. Predicted to be involved in kidney development; smoothened signaling pathway; and spermatogenesis. Predicted to act upstream of or within several processes, including left/right axis specification; lung development; and skeletal system development. Part of intraciliary transport particle B. [provided by Alliance of Genome Resources, Mar 2025]

SNORD51 Gene

small nucleolar RNA, C/D box 51

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD52 Gene

small nucleolar RNA, C/D box 52

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD53 Gene

small nucleolar RNA, C/D box 53

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD54 Gene

small nucleolar RNA, C/D box 54

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD55 Gene

small nucleolar RNA, C/D box 55

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD57 Gene

small nucleolar RNA, C/D box 57

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-24 Gene

small nucleolar RNA, C/D box 116-24

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-26 Gene

small nucleolar RNA, C/D box 116-26

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-22 Gene

small nucleolar RNA, C/D box 116-22

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-23 Gene

small nucleolar RNA, C/D box 116-23

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

KRR1P1 Gene

KRR1, small subunit (SSU) processome component, homolog (yeast) pseudogene 1

RNU1-14P Gene

RNA, U1 small nuclear 14, pseudogene

SNORD116-28 Gene

small nucleolar RNA, C/D box 116-28

LOC150417 Gene

small nuclear ribonucleoprotein polypeptide A' pseudogene

RNU6ATAC2P Gene

RNA, U6atac small nuclear 2, pseudogene

RNU5F-5P Gene

RNA, U5F small nuclear 5, pseudogene

SNRPA1 Gene

small nuclear ribonucleoprotein polypeptide A'

Enables RNA binding activity. Involved in mRNA splicing, via spliceosome and spermatogenesis. Located in nuclear speck. Part of U2-type catalytic step 2 spliceosome and U2-type precatalytic spliceosome. Implicated in connective tissue disease. [provided by Alliance of Genome Resources, Mar 2025]

UTP15 Gene

UTP15, U3 small nucleolar ribonucleoprotein, homolog (S. cerevisiae)

Enables RNA binding activity. Involved in positive regulation of rRNA processing; positive regulation of transcription by RNA polymerase I; and ribosomal small subunit biogenesis. Located in endoplasmic reticulum and fibrillar center. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA9L Gene

small Cajal body-specific RNA 9-like

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-71P Gene

RNA, U7 small nuclear 71 pseudogene

SNORA36B Gene

small nucleolar RNA, H/ACA box 36B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA36C Gene

small nucleolar RNA, H/ACA box 36C

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNVU1-3 Gene

RNA, variant U1 small nuclear 3

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-68P Gene

RNA, U6 small nuclear 68, pseudogene

RNU6-57P Gene

RNA, U6 small nuclear 57, pseudogene

SNORD115-18 Gene

small nucleolar RNA, C/D box 115-18

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-19 Gene

small nucleolar RNA, C/D box 115-19

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-15 Gene

small nucleolar RNA, C/D box 115-15

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-11 Gene

small nucleolar RNA, C/D box 115-11

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-12 Gene

small nucleolar RNA, C/D box 115-12

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-13 Gene

small nucleolar RNA, C/D box 115-13

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-14 Gene

small nucleolar RNA, C/D box 114-14

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

CAPNS1 Gene

calpain, small subunit 1

This gene is a member of the calpain small subunit family. Calpains are calcium-dependent cysteine proteinases that are widely distributed in mammalian cells. Calpains operate as heterodimers, comprising a specific large catalytic subunit (calpain 1 subunit in Calpain I, and calpain 2 subunit in Calpain II), and a common small regulatory subunit encoded by this gene. This encoded protein is essential for the stability and function of both calpain heterodimers, whose proteolytic activities influence various cellular functions including apoptosis, proliferation, migration, adhesion, and autophagy. Calpains have been implicated in neurodegenerative processes, such as myotonic dystrophy. A pseudogene of this gene has been defined on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]

CAPNS2 Gene

calpain, small subunit 2

Enables calcium-dependent cysteine-type endopeptidase activity. Predicted to be located in cytosol and plasma membrane. Predicted to be part of calpain complex. [provided by Alliance of Genome Resources, Mar 2025]

SNORD73B Gene

small nucleolar RNA, C/D box U73B (pseudogene)

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD73A Gene

small nucleolar RNA, C/D box 73A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNAR-I Gene

small ILF3/NF90-associated RNA I

LSM7 Gene

LSM7 homolog, U6 small nuclear RNA associated (S. cerevisiae)

Sm-like proteins were identified in a variety of organisms based on sequence homology with the Sm protein family (see SNRPD2; MIM 601061). Sm-like proteins contain the Sm sequence motif, which consists of 2 regions separated by a linker of variable length that folds as a loop. The Sm-like proteins are thought to form a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing.[supplied by OMIM, Apr 2004]

LSM1 Gene

LSM1, U6 small nuclear RNA associated

This gene encodes a member of the LSm family of RNA-binding proteins. LSm proteins form stable heteromers that bind specifically to the 3'-terminal oligo(U) tract of U6 snRNA and may play a role in pre-mRNA splicing by mediating U4/U6 snRNP formation. Increased expression of this gene may play a role in cellular transformation and the progression of several malignancies including lung cancer, mesothelioma and breast cancer. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the short arm of chromosome 9. [provided by RefSeq, Nov 2011]

LSM2 Gene

LSM2 homolog, U6 small nuclear RNA associated (S. cerevisiae)

This gene encodes a member of the LSm family of RNA-binding proteins. LSm proteins form stable heteromers that bind specifically to the 3'-terminal oligo(U) tract of U6 snRNA and may play a role in pre-mRNA splicing by mediating U4/U6 snRNP formation. Pseudogenes of this gene are located on the short arm of chromosomes 6 and 19. [provided by RefSeq, Nov 2011]

RNU6-72P Gene

RNA, U6 small nuclear 72, pseudogene

RNU5E-7P Gene

RNA, U5E small nuclear 7, pseudogene

RNU12 Gene

RNA, U12 small nuclear

Predicted to enable pre-mRNA branch point binding activity. Predicted to be involved in negative regulation of neuron apoptotic process. Predicted to act upstream of or within RNA splicing. Predicted to be part of U12 snRNP. Implicated in autosomal recessive spinocerebellar ataxia 33. [provided by Alliance of Genome Resources, Mar 2025]

RNU11 Gene

RNA, U11 small nuclear

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to act upstream of or within RNA splicing. Predicted to be part of U11 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNU4-8P Gene

RNA, U4 small nuclear 8, pseudogene

RNU7-58P Gene

RNA, U7 small nuclear 58 pseudogene

RNU5A-7P Gene

RNA, U5A small nuclear 7, pseudogene

RNU7-23P Gene

RNA, U7 small nuclear 23 pseudogene

SNORD109A Gene

small nucleolar RNA, C/D box 109A

This gene encodes a C/D box-type small nucleolar RNA that is expressed predominantly in the brain. Expression of this RNA is not detectable in the brains of patients with Prader-Willi syndrome. [provided by RefSeq, Jun 2010]

SNORD109B Gene

small nucleolar RNA, C/D box 109B

This gene encodes a C/D box-type small nucleolar RNA that is expressed predominantly in the brain. Expression of this RNA is not detectable in the brains of patients with Prader-Willi syndrome. [provided by RefSeq, Jun 2010]

SNORA70C Gene

small nucleolar RNA, H/ACA box 70C

This gene produces a small nucleolar RNA (snoRNA) that plays a role in post-transcriptional modification. This snoRNA is a type-3 retrotransposed snoRNA, where the ribosomal protein L10 gene on chromosome X is its parental gene, and this, together with part of the parental gene, was subsequently mobilized into an intron of the astrotactin 2 host gene on chromosome 9. This snoRNA contains a H/ACA box, which serves as a guide for the pseudouridylation of selected bases of ribosomal RNA by forming short duplexes with the 18S rRNA U1692, the target for this snoRNA. This gene is specific to human, chimp and orangutan, and is not found in the genomes of rhesus or marmoset. [provided by RefSeq, Jun 2010]

SNRPEP9 Gene

small nuclear ribonucleoprotein polypeptide E pseudogene 9

SNRPEP8 Gene

small nuclear ribonucleoprotein polypeptide E pseudogene 8

SNRPEP5 Gene

small nuclear ribonucleoprotein polypeptide E pseudogene 5

SNRPEP4 Gene

small nuclear ribonucleoprotein polypeptide E pseudogene 4

SNRPEP7 Gene

small nuclear ribonucleoprotein polypeptide E pseudogene 7

SNRPEP6 Gene

small nuclear ribonucleoprotein polypeptide E pseudogene 6

SNRPEP1 Gene

small nuclear ribonucleoprotein polypeptide E pseudogene 1

SNRPEP3 Gene

small nuclear ribonucleoprotein polypeptide E pseudogene 3

SNRPEP2 Gene

small nuclear ribonucleoprotein polypeptide E pseudogene 2

SNORA51 Gene

small nucleolar RNA, H/ACA box 51

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA11D Gene

small nucleolar RNA, H/ACA box 11D

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNRPCP1 Gene

small nuclear ribonucleoprotein polypeptide C pseudogene 1

SCARNA13 Gene

small Cajal body-specific RNA 13

Predicted to be involved in RNA processing. Located in Cajal body. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA12 Gene

small Cajal body-specific RNA 12

This gene produces a small nuclear RNA that localizes specifically to Cajal bodies, which are conserved subnuclear organelles that are present in the nucleoplasm. This RNA is processed from an intron of the prohibitin 2 host gene. It includes both an H/ACA box and a C/D box, and is thought to guide the pseudouridylation of residue U46 in the U5 small nuclear RNA. [provided by RefSeq, Jun 2010]

SCARNA11 Gene

small Cajal body-specific RNA 11

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA10 Gene

small Cajal body-specific RNA 10

Predicted to be involved in RNA processing. Located in Cajal body. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA17 Gene

small Cajal body-specific RNA 17

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA16 Gene

small Cajal body-specific RNA 16

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA15 Gene

small Cajal body-specific RNA 15

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. Predicted to be part of RISC complex. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA14 Gene

small Cajal body-specific RNA 14

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA18 Gene

small Cajal body-specific RNA 18

Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SCARNA18, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]

SMAP1 Gene

small ArfGAP 1

The protein encoded by this gene is similar to the mouse stromal membrane-associated protein-1. This similarity suggests that this human gene product is also a type II membrane glycoprotein involved in the erythropoietic stimulatory activity of stromal cells. Alternate splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jul 2008]

SMAP2 Gene

small ArfGAP2

Predicted to enable GTPase activator activity. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-89P Gene

RNA, U7 small nuclear 89 pseudogene

LOC101929087 Gene

small ubiquitin-related modifier 2-like

SNORA45B Gene

small nucleolar RNA, H/ACA box 45B

Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA45, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]

SNORA21 Gene

small nucleolar RNA, H/ACA box 21

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA24 Gene

small nucleolar RNA, H/ACA box 24

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA28 Gene

small nucleolar RNA, H/ACA box 28

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA29 Gene

small nucleolar RNA, H/ACA box 29

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD118 Gene

small nucleolar RNA, C/D box 118

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD119 Gene

small nucleolar RNA, C/D box 119

SNORD117 Gene

small nucleolar RNA, C/D box 117

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD112 Gene

small nucleolar RNA, C/D box 112

Small nucleolar RNAs (snoRNAs), like SNORD112, guide the formation of 2-prime O-methylation of ribosomal RNA (rRNA) and U small nuclear RNAs (snRNAs) through a specific RNA duplex at each modification site (Cavaille et al., 2002 [PubMed 12045206]).[supplied by OMIM, Nov 2010]

SNORD110 Gene

small nucleolar RNA, C/D box 110

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD111 Gene

small nucleolar RNA, C/D box 111

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-61P Gene

RNA, U7 small nuclear 61 pseudogene

SNORD11B Gene

small nucleolar RNA, C/D box 11B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-63P Gene

RNA, U7 small nuclear 63 pseudogene

SNRPGP2 Gene

small nuclear ribonucleoprotein polypeptide G pseudogene 2

SNAR-C5 Gene

small ILF3/NF90-associated RNA C5

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SNAR-C4 Gene

small ILF3/NF90-associated RNA C4

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SNAR-C1 Gene

small ILF3/NF90-associated RNA C1

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SNAR-C2 Gene

small ILF3/NF90-associated RNA C2

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

RNU12-2P Gene

RNA, U12 small nuclear 2, pseudogene

SCARNA9 Gene

small Cajal body-specific RNA 9

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA8 Gene

small Cajal body-specific RNA 8

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA7 Gene

small Cajal body-specific RNA 7

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA3 Gene

small Cajal body-specific RNA 3

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SCARNA1 Gene

small Cajal body-specific RNA 1

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNRPEP10 Gene

small nuclear ribonucleoprotein polypeptide E pseudogene 10

RNU7-46P Gene

RNA, U7 small nuclear 46 pseudogene

SNORD36A Gene

small nucleolar RNA, C/D box 36A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD36C Gene

small nucleolar RNA, C/D box 36C

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD36B Gene

small nucleolar RNA, C/D box 36B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU5A-1 Gene

RNA, U5A small nuclear 1

Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U5 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

SNORA38B Gene

small nucleolar RNA, H/ACA box 38B

Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-35P Gene

RNA, U6 small nuclear 35, pseudogene

SNRPD2P2 Gene

small nuclear ribonucleoprotein D2 pseudogene 2

SNRPD2P1 Gene

small nuclear ribonucleoprotein D2 pseudogene 1

SNORD116-9 Gene

small nucleolar RNA, C/D box 116-9

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-8 Gene

small nucleolar RNA, C/D box 116-8

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-4 Gene

small nucleolar RNA, C/D box 116-4

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-1 Gene

small nucleolar RNA, C/D box 116-1

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-3 Gene

small nucleolar RNA, C/D box 116-3

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-2 Gene

small nucleolar RNA, C/D box 116-2

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-40P Gene

RNA, U7 small nuclear 40 pseudogene

RNU7-69P Gene

RNA, U7 small nuclear 69 pseudogene

RNU7-34P Gene

RNA, U7 small nuclear 34 pseudogene

SNORD19B Gene

small nucleolar RNA, C/D box 19B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU5B-4P Gene

RNA, U5B small nuclear 4, pseudogene

RNU7-55P Gene

RNA, U7 small nuclear 55 pseudogene

RNU5A-3P Gene

RNA, U5A small nuclear 3, pseudogene

SNORD21 Gene

small nucleolar RNA, C/D box 21

This gene encodes a small nucleolar RNA (snoRNA) that may be involved in biogenesis of the large (28S) ribosomal subunit. This gene is found within an intron of the RPL5 gene. [provided by RefSeq, Mar 2009]

SNORD20 Gene

small nucleolar RNA, C/D box 20

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD22 Gene

small nucleolar RNA, C/D box 22

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD25 Gene

small nucleolar RNA, C/D box 25

SNORD24 Gene

small nucleolar RNA, C/D box 24

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD27 Gene

small nucleolar RNA, C/D box 27

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD26 Gene

small nucleolar RNA, C/D box 26

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD29 Gene

small nucleolar RNA, C/D box 29

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD28 Gene

small nucleolar RNA, C/D box 28

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU105C Gene

RNA, U105C small nucleolar

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

LOC100422088 Gene

ash2 (absent, small, or homeotic)-like (Drosophila) pseudogene

SNAR-A9 Gene

small ILF3/NF90-associated RNA A9

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-26P Gene

RNA, U7 small nuclear 26 pseudogene

SNAR-A1 Gene

small ILF3/NF90-associated RNA A1

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SNRPN Gene

small nuclear ribonucleoprotein polypeptide N

This gene is located within the Prader-Willi Syndrome critical region on chromosome 15 and is imprinted and expressed from the paternal allele. It encodes a component of the small nuclear ribonucleoprotein complex, which functions in pre-mRNA processing and may contribute to tissue-specific alternative splicing. Alternative promoter use and alternative splicing result in a multitude of transcript variants encoding the same protein. Transcript variants that initiate at the CpG island-associated imprinting center may be bicistronic and also encode the SNRPN upstream reading frame protein (SNURF) from an upstream open reading frame. In addition, long spliced transcripts for small nucleolar RNA host gene 14 (SNHG14) may originate from the promoters at this locus and share exons with this gene. Alterations in this region are associated with parental imprint switch failure, which may cause Angelman syndrome or Prader-Willi syndrome. [provided by RefSeq, Mar 2017]

SNRPB Gene

small nuclear ribonucleoprotein polypeptides B and B1

The protein encoded by this gene is one of several nuclear proteins that are found in common among U1, U2, U4/U6, and U5 small ribonucleoprotein particles (snRNPs). These snRNPs are involved in pre-mRNA splicing, and the encoded protein may also play a role in pre-mRNA splicing or snRNP structure. Autoantibodies from patients with systemic lupus erythematosus frequently recognize epitopes on the encoded protein. Two transcript variants encoding different isoforms (B and B') have been found for this gene. [provided by RefSeq, Jul 2008]

SNRPC Gene

small nuclear ribonucleoprotein polypeptide C

This gene encodes one of the specific protein components of the U1 small nuclear ribonucleoprotein (snRNP) particle required for the formation of the spliceosome. The encoded protein participates in the processing of nuclear precursor messenger RNA splicing. snRNP particles are attacked by autoantibodies frequently produced by patients with connective tissue diseases. The genome contains several pseudogenes of this functional gene. Alternative splicing results in a non-coding transcript variant.[provided by RefSeq, Oct 2009]

SNRPA Gene

small nuclear ribonucleoprotein polypeptide A

The protein encoded by this gene associates with stem loop II of the U1 small nuclear ribonucleoprotein, which binds the 5' splice site of precursor mRNAs and is required for splicing. The encoded protein autoregulates itself by polyadenylation inhibition of its own pre-mRNA via dimerization and has been implicated in the coupling of splicing and polyadenylation. [provided by RefSeq, Oct 2010]

SNRPF Gene

small nuclear ribonucleoprotein polypeptide F

Enables RNA binding activity. Involved in spliceosomal snRNP assembly. Located in cytosol and nucleus. Part of several cellular components, including methylosome; nucleus; and pICln-Sm protein complex. Biomarker of nasopharynx carcinoma. [provided by Alliance of Genome Resources, Mar 2025]

SNRPG Gene

small nuclear ribonucleoprotein polypeptide G

The protein encoded by this gene is a component of the U1, U2, U4, and U5 small nuclear ribonucleoprotein complexes, precursors of the spliceosome. The encoded protein may also be a part of the U7 small nuclear ribonucleoprotein complex, which participates in the processing of the 3' end of histone transcripts. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2015]

SNRPE Gene

small nuclear ribonucleoprotein polypeptide E

The protein encoded by this gene is a core component of U small nuclear ribonucleoproteins, which are key components of the pre-mRNA processing spliceosome. The encoded protein plays a role in the 3' end processing of histone transcripts. This protein is one of the targets in the autoimmune disease systemic lupus erythematosus, and mutations in this gene have been associated with hypotrichosis. Several pseudogenes of this gene have been identified. [provided by RefSeq, Jun 2016]

CAPNS1P1 Gene

calpain, small subunit 1 pseudogene 1

RNVU1-8 Gene

RNA, variant U1 small nuclear 8

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNVU1-4 Gene

RNA, variant U1 small nuclear 4

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNVU1-6 Gene

RNA, variant U1 small nuclear 6

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be located in nucleus. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNVU1-7 Gene

RNA, variant U1 small nuclear 7

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNVU1-1 Gene

RNA, variant U1 small nuclear 1

SNORA20 Gene

small nucleolar RNA, H/ACA box 20

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA22 Gene

small nucleolar RNA, H/ACA box 22

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA23 Gene

small nucleolar RNA, H/ACA box 23

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA25 Gene

small nucleolar RNA, H/ACA box 25

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA26 Gene

small nucleolar RNA, H/ACA box 26

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA27 Gene

small nucleolar RNA, H/ACA box 27

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA2A Gene

small nucleolar RNA, H/ACA box 2A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA2B Gene

small nucleolar RNA, H/ACA box 2B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SERF1AP1 Gene

small EDRK-rich factor 1A (telomeric) pseudogene 1

U2AF1 Gene

U2 small nuclear RNA auxiliary factor 1

This gene belongs to the splicing factor SR family of genes. U2 auxiliary factor, comprising a large and a small subunit, is a non-snRNP protein required for the binding of U2 snRNP to the pre-mRNA branch site. This gene encodes the small subunit which plays a critical role in both constitutive and enhancer-dependent RNA splicing by directly mediating interactions between the large subunit and proteins bound to the enhancers. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

U2AF2 Gene

U2 small nuclear RNA auxiliary factor 2

U2 auxiliary factor (U2AF), comprised of a large and a small subunit, is a non-snRNP protein required for the binding of U2 snRNP to the pre-mRNA branch site. This gene encodes the U2AF large subunit which contains a sequence-specific RNA-binding region with 3 RNA recognition motifs and an Arg/Ser-rich domain necessary for splicing. The large subunit binds to the polypyrimidine tract of introns early during spliceosome assembly. Multiple transcript variants have been detected for this gene, but the full-length natures of only two have been determined to date. [provided by RefSeq, Jul 2008]

RNU6-75P Gene

RNA, U6 small nuclear 75, pseudogene

SNORD56B Gene

small nucleolar RNA, C/D box 56B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU5E-4P Gene

RNA, U5E small nuclear 4, pseudogene

SNRPCP19 Gene

small nuclear ribonucleoprotein polypeptide C pseudogene 19

SNRPCP18 Gene

small nuclear ribonucleoprotein polypeptide C pseudogene 18

SNRPCP15 Gene

small nuclear ribonucleoprotein polypeptide C pseudogene 15

SNRPCP14 Gene

small nuclear ribonucleoprotein polypeptide C pseudogene 14

SNRPCP12 Gene

small nuclear ribonucleoprotein polypeptide C pseudogene 12

SNRPCP11 Gene

small nuclear ribonucleoprotein polypeptide C pseudogene 11

SNORD116-20 Gene

small nucleolar RNA, C/D box 116-20

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-29 Gene

small nucleolar RNA, C/D box 116-29

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU1-11P Gene

RNA, U1 small nuclear 11, pseudogene

RNU7-7P Gene

RNA, U7 small nuclear 7 pseudogene

LOC100130842 Gene

small integral membrane protein 7 pseudogene

RNU6-81P Gene

RNA, U6 small nuclear 81, pseudogene

RNU7-76P Gene

RNA, U7 small nuclear 76 pseudogene

UTP23 Gene

UTP23, small subunit (SSU) processome component, homolog (yeast)

Enables mRNA 3'-UTR binding activity and mRNA 5'-UTR binding activity. Predicted to be involved in rRNA processing. Predicted to act upstream of or within endonucleolytic cleavage in 5'-ETS of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA). Predicted to be located in nucleus. Predicted to be part of small-subunit processome. Predicted to be active in nucleolus. Implicated in colorectal adenocarcinoma. [provided by Alliance of Genome Resources, Mar 2025]

UTP20 Gene

UTP20, small subunit (SSU) processome component, homolog (yeast)

UTP20 is a component of the U3 small nucleolar RNA (snoRNA) (SNORD3A; MIM 180710) protein complex (U3 snoRNP) and is involved in 18S rRNA processing (Wang et al., 2007 [PubMed 17498821]).[supplied by OMIM, Jun 2009]

RNU4-2 Gene

RNA, U4 small nuclear 2

Predicted to enable U6 snRNA binding activity. Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4 snRNP and U4/U6 x U5 tri-snRNP complex. [provided by Alliance of Genome Resources, Mar 2025]

SNRPFP4 Gene

small nuclear ribonucleoprotein polypeptide F pseudogene 4

SNRPFP2 Gene

small nuclear ribonucleoprotein polypeptide F pseudogene 2

SNRPFP1 Gene

small nuclear ribonucleoprotein polypeptide F pseudogene 1

SNHG10 Gene

small nucleolar RNA host gene 10

This gene is small nucleolar RNA host gene 10 and represents a non-protein coding RNA. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2013]

SUMO1 Gene

small ubiquitin-like modifier 1

This gene encodes a protein that is a member of the SUMO (small ubiquitin-like modifier) protein family. It functions in a manner similar to ubiquitin in that it is bound to target proteins as part of a post-translational modification system. However, unlike ubiquitin which targets proteins for degradation, this protein is involved in a variety of cellular processes, such as nuclear transport, transcriptional regulation, apoptosis, and protein stability. It is not active until the last four amino acids of the carboxy-terminus have been cleaved off. Several pseudogenes have been reported for this gene. Alternate transcriptional splice variants encoding different isoforms have been characterized. [provided by RefSeq, Jul 2008]

SUMO2 Gene

small ubiquitin-like modifier 2

This gene encodes a protein that is a member of the SUMO (small ubiquitin-like modifier) protein family. It functions in a manner similar to ubiquitin in that it is bound to target proteins as part of a post-translational modification system. However, unlike ubiquitin which targets proteins for degradation, this protein is involved in a variety of cellular processes, such as nuclear transport, transcriptional regulation, apoptosis, and protein stability. It is not active until the last two amino acids of the carboxy-terminus have been cleaved off. Numerous pseudogenes have been reported for this gene. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]

SUMO4 Gene

small ubiquitin-like modifier 4

This gene is a member of the SUMO gene family. This family of genes encode small ubiquitin-related modifiers that are attached to proteins and control the target proteins' subcellular localization, stability, or activity. The protein described in this record is located in the cytoplasm and specifically modifies IKBA, leading to negative regulation of NF-kappa-B-dependent transcription of the IL12B gene. A specific polymorphism in this SUMO gene, which leads to the M55V substitution, has been associated with type I diabetes. The RefSeq contains this polymorphism. [provided by RefSeq, Jul 2008]

LOC100652840 Gene

M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene

RNU4-5P Gene

RNA, U4 small nuclear 5, pseudogene

SNRPGP3 Gene

small nuclear ribonucleoprotein polypeptide G pseudogene 3

LOC100129492 Gene

small nuclear ribonucleoprotein Sm D1 pseudogene

SGSM2 Gene

small G protein signaling modulator 2

The protein encoded by this gene is a GTPase activator with activity towards RAB32 and RAB33B, which are regulators of membrane trafficking. The encoded protein inactivates RAB32 and can bind RAB9A-GTP, a protein required for RAB32 activation. [provided by RefSeq, Oct 2016]

SGSM1 Gene

small G protein signaling modulator 1

Enables GTPase activator activity and small GTPase binding activity. Predicted to act upstream of or within positive regulation of transcription by RNA polymerase II. Located in cytoplasmic vesicle membrane and cytosol. [provided by Alliance of Genome Resources, Mar 2025]

SNORA14B Gene

small nucleolar RNA, H/ACA box 14B

Small nucleolar RNAs (snoRNAs) are 60-150 nt long non-coding RNAs, and include two groups: C/D box snoRNAs and H/ACA box snoRNAs. The C/D box snoRNAs are guides for the 2'-O-ribose methylation of rRNAs or snRNAs. The H/ACA box snoRNAs are guides for the isomerization of uridine residues into pseudouridine. This gene belongs to the group of the H/ACA box snoRNAs, and functions in 18S rRNA pseudouridylation at position U966. The gene duplication generates a 91% identical copy on chromosome 7. [provided by RefSeq, Oct 2008]

SNORA14A Gene

small nucleolar RNA, H/ACA box 14A

Small nucleolar RNAs (snoRNAs) are 60-150 nt long non-coding RNAs, and include two groups: C/D box snoRNAs and H/ACA box snoRNAs. The C/D box snoRNAs are guides for the 2'-O-ribose methylation of rRNAs or snRNAs. The H/ACA box snoRNAs are guides for the isomerization of uridine residues into pseudouridine. This gene belongs to the group of the H/ACA box snoRNAs, and functions in 18S rRNA pseudouridylation at position U966. The gene duplication generates a 91% identical copy on chromosome 1. [provided by RefSeq, Oct 2008]

RNU4-10P Gene

RNA, U4 small nuclear 10, pseudogene

LOC101929240 Gene

U5 small nuclear ribonucleoprotein 200 kDa helicase pseudogene

RNU1-19P Gene

RNA, U1 small nuclear 19, pseudogene

RNU6-14P Gene

RNA, U6 small nuclear 14, pseudogene

RNU5F-8P Gene

RNA, U5F small nuclear 8, pseudogene

SNORD35A Gene

small nucleolar RNA, C/D box 35A

Predicted to be involved in RNA processing. Predicted to act upstream of or within glucose metabolic process; insulin secretion; and reactive oxygen species metabolic process. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD35B Gene

small nucleolar RNA, C/D box 35B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SMIM10L2A Gene

small integral membrane protein 10 like 2A

This gene encodes a highly conserved small protein that contains a conserved motif (DUF4560) and may function as an integral membrane protein. This transcript was also shown to associate with enhancer chromatin and therefore may also function as an RNA to regulate enhancers. [provided by RefSeq, Jan 2017]

RNU7-45P Gene

RNA, U7 small nuclear 45 pseudogene

RNU7-84P Gene

RNA, U7 small nuclear 84 pseudogene

RNU6-30P Gene

RNA, U6 small nuclear 30, pseudogene

SNORD13P1 Gene

small nucleolar RNA, C/D box 13 pseudogene 1

SNORD13P3 Gene

small nucleolar RNA, C/D box 13 pseudogene 3

SNORD13P2 Gene

small nucleolar RNA, C/D box 13 pseudogene 2

RNU6-78P Gene

RNA, U6 small nuclear 78, pseudogene

LOC100422645 Gene

CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase 2 pseudogene

RNU7-39P Gene

RNA, U7 small nuclear 39 pseudogene

SNORD14E Gene

small nucleolar RNA, C/D box 14E

SNORD14D Gene

small nucleolar RNA, C/D box 14D

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD14A Gene

small nucleolar RNA, C/D box 14A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD14C Gene

small nucleolar RNA, C/D box 14C

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD14B Gene

small nucleolar RNA, C/D box 14B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD49A Gene

small nucleolar RNA, C/D box 49A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-64P Gene

RNA, U7 small nuclear 64 pseudogene

LOC100533850 Gene

M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene

RNU7-70P Gene

RNA, U7 small nuclear 70 pseudogene

SNORA37 Gene

small nucleolar RNA, H/ACA box 37

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-56P Gene

RNA, U7 small nuclear 56 pseudogene

RNU5F-1 Gene

RNA, U5F small nuclear 1

Predicted to be involved in formation of quadruple SL/U4/U5/U6 snRNP and spliceosomal tri-snRNP complex assembly. Predicted to be part of U4/U6 x U5 tri-snRNP complex and U5 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

SNORD62A Gene

small nucleolar RNA, C/D box 62A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-22 Gene

small nucleolar RNA, C/D box 114-22

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-23 Gene

small nucleolar RNA, C/D box 114-23

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-21 Gene

small nucleolar RNA, C/D box 114-21

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-26 Gene

small nucleolar RNA, C/D box 114-26

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-27 Gene

small nucleolar RNA, C/D box 114-27

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-24 Gene

small nucleolar RNA, C/D box 114-24

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-25 Gene

small nucleolar RNA, C/D box 114-25

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-28 Gene

small nucleolar RNA, C/D box 114-28

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-29 Gene

small nucleolar RNA, C/D box 114-29

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-15P Gene

RNA, U7 small nuclear 15 pseudogene

RNU1-1 Gene

RNA, U1 small nuclear 1

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

RNU1-4 Gene

RNA, U1 small nuclear 4

Predicted to enable pre-mRNA 5'-splice site binding activity. Predicted to be involved in mRNA 5'-splice site recognition. Predicted to be part of U1 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

SNAR-H Gene

small ILF3/NF90-associated RNA H

LOC100631375 Gene

M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene

RNU6-59P Gene

RNA, U6 small nuclear 59, pseudogene

RNU7-31P Gene

RNA, U7 small nuclear 31 pseudogene

LOC105379766 Gene

small nuclear ribonucleoprotein-associated protein N-like

SNORA5A Gene

small nucleolar RNA, H/ACA box 5A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA5C Gene

small nucleolar RNA, H/ACA box 5C

Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SNORA5C, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008]

SNORA5B Gene

small nucleolar RNA, H/ACA box 5B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA58 Gene

small nucleolar RNA, H/ACA box 58

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. Predicted to be part of RISC complex. [provided by Alliance of Genome Resources, Mar 2025]

SNORA52 Gene

small nucleolar RNA, H/ACA box 52

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA55 Gene

small nucleolar RNA, H/ACA box 55

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA54 Gene

small nucleolar RNA, H/ACA box 54

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA57 Gene

small nucleolar RNA, H/ACA box 57

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA56 Gene

small nucleolar RNA, H/ACA box 56

Biosynthesis of stable cellular RNAs such as tRNAs, rRNAs, snRNAs, and snoRNAs is aided by covalent nucleotide modification after transcription. The modified nucleotides are involved in correct RNA folding, establishment of correct RNA-RNA and RNA-protein interactions, and in the correct function of mature RNAs. The RNA encoded by this gene is thought to mediate the pseudouridylation of residue U1664 of 28S rRNA. [provided by RefSeq, Feb 2009]

RNU5B-2P Gene

RNA, U5B small nuclear 2, pseudogene

RNU5E-3P Gene

RNA, U5E small nuclear 3, pseudogene

RNU7-50P Gene

RNA, U7 small nuclear 50 pseudogene

RNU5A-6P Gene

RNA, U5A small nuclear 6, pseudogene

SCARNA6 Gene

small Cajal body-specific RNA 6

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU5E-10P Gene

RNA, U5E small nuclear 10, pseudogene

SNORD116-19 Gene

small nucleolar RNA, C/D box 116-19

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-18 Gene

small nucleolar RNA, C/D box 116-18

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-11 Gene

small nucleolar RNA, C/D box 116-11

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-13 Gene

small nucleolar RNA, C/D box 116-13

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-15 Gene

small nucleolar RNA, C/D box 116-15

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-14 Gene

small nucleolar RNA, C/D box 116-14

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-17 Gene

small nucleolar RNA, C/D box 116-17

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD116-16 Gene

small nucleolar RNA, C/D box 116-16

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-29P Gene

RNA, U7 small nuclear 29 pseudogene

SNORD59B Gene

small nucleolar RNA, C/D box 59B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD59A Gene

small nucleolar RNA, C/D box 59A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNRPBP1 Gene

small nuclear ribonucleoprotein polypeptides B and B1 pseudogene 1

LOC100128056 Gene

CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase 2 pseudogene

SNORD72 Gene

small nucleolar RNA, C/D box 72

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD77 Gene

small nucleolar RNA, C/D box 77

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD74 Gene

small nucleolar RNA, C/D box 74

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD75 Gene

small nucleolar RNA, C/D box 75

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD78 Gene

small nucleolar RNA, C/D box 78

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD79 Gene

small nucleolar RNA, C/D box 79

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-79P Gene

RNA, U7 small nuclear 79 pseudogene

RNU6-28P Gene

RNA, U6 small nuclear 28, pseudogene

SNRPFP3 Gene

small nuclear ribonucleoprotein polypeptide F pseudogene 3

RNU2-5P Gene

RNA, U2 small nuclear 5, pseudogene

SNORD56 Gene

small nucleolar RNA, C/D box 56

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD113-8 Gene

small nucleolar RNA, C/D box 113-8

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD113-9 Gene

small nucleolar RNA, C/D box 113-9

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD113-4 Gene

small nucleolar RNA, C/D box 113-4

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD113-5 Gene

small nucleolar RNA, C/D box 113-5

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD113-6 Gene

small nucleolar RNA, C/D box 113-6

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD113-7 Gene

small nucleolar RNA, C/D box 113-7

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD113-2 Gene

small nucleolar RNA, C/D box 113-2

SNORD96B Gene

small nucleolar RNA, C/D box 96B

SNORD96A Gene

small nucleolar RNA, C/D box 96A

RNU5F-3P Gene

RNA, U5F small nuclear 3, pseudogene

SNORD38B Gene

small nucleolar RNA, C/D box 38B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD38A Gene

small nucleolar RNA, C/D box 38A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

LSM10 Gene

LSM10, U7 small nuclear RNA associated

Enables U7 snRNA binding activity. Involved in positive regulation of G1/S transition of mitotic cell cycle. Located in Cajal body. Part of U7 snRNP. [provided by Alliance of Genome Resources, Mar 2025]

LSM11 Gene

LSM11, U7 small nuclear RNA associated

Enables U7 snRNA binding activity. Involved in mRNA 3'-end processing by stem-loop binding activity and cleavage; positive regulation of G1/S transition of mitotic cell cycle; and regulation of chromatin organization. Located in nuclear body. Part of U7 snRNP and telomerase holoenzyme complex. Implicated in Aicardi-Goutieres syndrome. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-48P Gene

RNA, U7 small nuclear 48 pseudogene

SNORD115-34 Gene

small nucleolar RNA, C/D box 115-34

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-35 Gene

small nucleolar RNA, C/D box 115-35

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-32 Gene

small nucleolar RNA, C/D box 115-32

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-38 Gene

small nucleolar RNA, C/D box 115-38

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD115-39 Gene

small nucleolar RNA, C/D box 115-39

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNHG20 Gene

small nucleolar RNA host gene 20

Predicted to be involved in several processes, including cellular response to fatty acid; macrophage activation; and tyrosine phosphorylation of STAT protein. Implicated in lung non-small cell carcinoma. [provided by Alliance of Genome Resources, Mar 2025]

SNHG21 Gene

small nucleolar RNA host gene 21

SNHG22 Gene

small nucleolar RNA host gene 22

SNHG23 Gene

small nucleolar RNA host gene 23

SNHG24 Gene

small nucleolar RNA host gene 24

RNU6-42P Gene

RNA, U6 small nuclear 42, pseudogene

SNORD115@ Gene

small nucleolar RNA, C/D box 115 cluster

SNORA59A Gene

small nucleolar RNA, H/ACA box 59A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA59B Gene

small nucleolar RNA, H/ACA box 59B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

LOC728825 Gene

small ubiquitin-like modifier 2

RNU7-21P Gene

RNA, U7 small nuclear 21 pseudogene

SNORD71 Gene

small nucleolar RNA, C/D box 71

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD76 Gene

small nucleolar RNA, C/D box 76

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA11C Gene

small nucleolar RNA, H/ACA box 11C

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORA11B Gene

small nucleolar RNA, H/ACA box 11B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNRNP35 Gene

small nuclear ribonucleoprotein 35kDa (U11/U12)

The protein encoded by this gene is a homolog of the U1-snRNP binding protein. The N-terminal half contains a RNA recognition motif and the C-terminal half is rich in Arg/Asp and Arg/Glu dipeptides, which is a characteristic of a variety of splicing factors. This protein is a component of the U11/U12 small nuclear ribonucleoproteins (snRNP) that form part of the U12-type spliceosome. Alternative splicing results in multiple transcript variants encoding two distinct isoforms and representing a non-protein coding variant. [provided by RefSeq, Aug 2013]

SMPX Gene

small muscle protein, X-linked

This gene encodes a small protein that has no known functional domains. Mutations in this gene are a cause of X-linked deafness-4, and the encoded protein may play a role in the maintenance of inner ear cells subjected to mechanical stress. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Dec 2011]

RNU7-3P Gene

RNA, U7 small nuclear 3 pseudogene

SNORD6 Gene

small nucleolar RNA, C/D box 6

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD7 Gene

small nucleolar RNA, C/D box 7

This gene encodes a spliceosomal small nuclear RNA that has orthologs in S. pombe and D. melanogaster. In S. pombe, this gene is required for site-specific 2'-O-methylation of U6 snRNA at position A41. While this is not an essential gene for S. pombe growth, loss of this gene's function may result in a slight decrease in mRNA splicing efficiency. [provided by RefSeq, Oct 2008]

SNORD5 Gene

small nucleolar RNA, C/D box 5

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD2 Gene

small nucleolar RNA, C/D box 2

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD8 Gene

small nucleolar RNA, C/D box 8

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD9 Gene

small nucleolar RNA, C/D box 9

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

ASH2L Gene

ash2 (absent, small, or homeotic)-like (Drosophila)

Enables beta-catenin binding activity and transcription cis-regulatory region binding activity. Involved in positive regulation of cell population proliferation; response to estrogen; and transcription initiation-coupled chromatin remodeling. Acts upstream of or within DNA damage response. Located in nucleus. Part of MLL1 complex; MLL3/4 complex; and Set1C/COMPASS complex. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-2P Gene

RNA, U7 small nuclear 2 pseudogene

RNU2-7P Gene

RNA, U2 small nuclear 7, pseudogene

SMLR1 Gene

small leucine-rich protein 1

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-8 Gene

small nucleolar RNA, C/D box 114-8

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SPRR2E Gene

small proline-rich protein 2E

This gene encodes a member of a family of small proline-rich proteins clustered in the epidermal differentiation complex on chromosome 1q21. The encoded protein, along with other family members, is a component of the cornified cell envelope that forms beneath the plasma membrane in terminally differentiated stratified squamous epithelia. This envelope serves as a barrier against extracellular and environmental factors. The seven SPRR2 genes (A-G) appear to have been homogenized by gene conversion compared to others in the cluster that exhibit greater differences in protein structure. [provided by RefSeq, Feb 2014]

SPRR2D Gene

small proline-rich protein 2D

Predicted to be involved in female gonad development. Predicted to act upstream of or within response to estradiol. Located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025]

SPRR2G Gene

small proline-rich protein 2G

Predicted to be involved in keratinocyte differentiation. Predicted to act upstream of or within response to estradiol. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SPRR2F Gene

small proline-rich protein 2F

Predicted to be involved in keratinocyte differentiation. Predicted to act upstream of or within response to estradiol. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SPRR2A Gene

small proline-rich protein 2A

Enables lipid binding activity. Involved in antibacterial humoral response and defense response to Gram-positive bacterium. Located in cytoplasm. Is active in extracellular region and secretory granule. [provided by Alliance of Genome Resources, Mar 2025]

SPRR2C Gene

small proline-rich protein 2C (pseudogene)

SPRR2B Gene

small proline-rich protein 2B

Predicted to be involved in keratinocyte differentiation. Predicted to act upstream of or within response to estradiol. Predicted to be located in cornified envelope and cytosol. [provided by Alliance of Genome Resources, Mar 2025]

RNU6-33P Gene

RNA, U6 small nuclear 33, pseudogene

LSM3 Gene

LSM3 homolog, U6 small nuclear RNA associated (S. cerevisiae)

Sm-like proteins were identified in a variety of organisms based on sequence homology with the Sm protein family (see SNRPD2; MIM 601061). Sm-like proteins contain the Sm sequence motif, which consists of 2 regions separated by a linker of variable length that folds as a loop. The Sm-like proteins are thought to form a stable heteromer present in tri-snRNP particles, which are important for pre-mRNA splicing.[supplied by OMIM, Apr 2004]

SUMO3 Gene

small ubiquitin-like modifier 3

This gene encodes a member of the small ubiquitin-related modifier (SUMO) family of eukaryotic proteins. The encoded protein is covalently conjugated to other proteins via a post-translation modification known as sumoylation. Sumoylation may play a role in a wide variety of cellular processes, including nuclear transport, DNA replication and repair, mitosis, transcriptional regulation, and signal transduction. Alternatively spliced transcript variants encoding distinct proteins have been described. [provided by RefSeq, Feb 2014]

RNU7-67P Gene

RNA, U7 small nuclear 67 pseudogene

CTDSPL2 Gene

CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2

Enables RNA polymerase II CTD heptapeptide repeat phosphatase activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of BMP signaling pathway; positive regulation of protein export from nucleus; and protein dephosphorylation. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025]

SNORD103B Gene

small nucleolar RNA, C/D box 103B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD103A Gene

small nucleolar RNA, C/D box 103A

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-9 Gene

small nucleolar RNA, C/D box 114-9

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-3 Gene

small nucleolar RNA, C/D box 114-3

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-2 Gene

small nucleolar RNA, C/D box 114-2

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-7 Gene

small nucleolar RNA, C/D box 114-7

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-19 Gene

small nucleolar RNA, C/D box 114-19

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-18 Gene

small nucleolar RNA, C/D box 114-18

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-13 Gene

small nucleolar RNA, C/D box 114-13

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-12 Gene

small nucleolar RNA, C/D box 114-12

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-11 Gene

small nucleolar RNA, C/D box 114-11

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-10 Gene

small nucleolar RNA, C/D box 114-10

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-17 Gene

small nucleolar RNA, C/D box 114-17

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-16 Gene

small nucleolar RNA, C/D box 114-16

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNORD114-15 Gene

small nucleolar RNA, C/D box 114-15

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-83P Gene

RNA, U7 small nuclear 83 pseudogene

SNAR-A13 Gene

small ILF3/NF90-associated RNA A13

Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

RNU7-16P Gene

RNA, U7 small nuclear 16 pseudogene

UTP4 Gene

UTP4 small subunit processome component

This gene encodes a WD40-repeat-containing protein that is localized to the nucleolus. Mutation of this gene causes North American Indian childhood cirrhosis, a severe intrahepatic cholestasis that results in transient neonatal jaundice, and progresses to periportal fibrosis and cirrhosis in childhood and adolescence. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]

SNU13 Gene

small nuclear ribonucleoprotein 13

Originally named because of its sequence similarity to the Saccharomyces cerevisiae NHP2 (non-histone protein 2), this protein appears to be a highly conserved nuclear protein that is a component of the [U4/U6.U5] tri-snRNP. It binds to the 5' stem-loop of U4 snRNA. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]

UTP11 Gene

UTP11 small subunit processome component

Enables RNA binding activity. Involved in nervous system development; positive regulation of apoptotic process; and ribosomal small subunit biogenesis. Located in cytoplasm; extracellular space; and nucleolus. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025]

UTP25 Gene

UTP25 small subunit processome component

Enables RNA binding activity. Involved in several processes, including protein catabolic process; protein destabilization; and protein localization to nucleolus. Located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SMIM26 Gene

small integral membrane protein 26

Enables protein kinase binding activity and transmembrane transporter binding activity. Located in mitochondrial outer membrane. [provided by Alliance of Genome Resources, Mar 2025]

SVBP Gene

small vasohibin binding protein

Enables microtubule binding activity and peptidase activator activity. Involved in axon development; proteolysis; and regulation of metallopeptidase activity. Acts upstream of or within negative regulation of endothelial cell migration; negative regulation of protein ubiquitination; and protein secretion. Located in apical part of cell. [provided by Alliance of Genome Resources, Mar 2025]

SMIM41 Gene

small integral membrane protein 41

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SCYGR4 Gene

small cysteine and glycine repeat containing 4

Predicted to be located in intermediate filament. [provided by Alliance of Genome Resources, Mar 2025]

SMIM36 Gene

small integral membrane protein 36

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM33 Gene

small integral membrane protein 33

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM40 Gene

small integral membrane protein 40

Predicted to be located in membrane. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SMIM38 Gene

small integral membrane protein 38

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SNHG32 Gene

small nucleolar RNA host gene 32

Predicted to enable double-stranded RNA binding activity. [provided by Alliance of Genome Resources, Mar 2025]

SMIM27 Gene

small integral membrane protein 27

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM29 Gene

small integral membrane protein 29

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM31 Gene

small integral membrane protein 31

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM35 Gene

small integral membrane protein 35

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM43 Gene

small integral membrane protein 43

Enables transmembrane transporter binding activity. Predicted to be involved in mesendoderm development. Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025]

SPAAR Gene

small regulatory polypeptide of amino acid response

Involved in cellular response to amino acid stimulus and negative regulation of TORC1 signaling. Located in late endosome membrane and lysosomal proton-transporting V-type ATPase complex. [provided by Alliance of Genome Resources, Mar 2025]

SMIM45 Gene

small integral membrane protein 45

Involved in neuron maturation. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025]

SMIM30 Gene

small integral membrane protein 30

Involved in negative regulation of type I interferon-mediated signaling pathway. Located in endoplasmic reticulum membrane and mitochondrial membrane. [provided by Alliance of Genome Resources, Mar 2025]

SNHG25 Gene

small nucleolar RNA host gene 25

SNHG28 Gene

small nucleolar RNA host gene 28

Enables RNA binding activity. [provided by Alliance of Genome Resources, Mar 2025]

SNHG29 Gene

small nucleolar RNA host gene 29

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNHG30 Gene

small nucleolar RNA host gene 30

RNU6-645P Gene

RNA, U6 small nuclear 645, pseudogene

SNORA17B Gene

small nucleolar RNA, H/ACA box 17B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SMIM44 Gene

small integral membrane protein 44

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SNORA63B Gene

small nucleolar RNA, H/ACA box 63B

Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025]

SNHG26 Gene

small nucleolar RNA host gene 26

SPRR5 Gene

small proline rich protein 5

STRIT1 Gene

small transmembrane regulator of ion transport 1

Predicted to enable enzyme activator activity. Predicted to be involved in regulation of calcium ion transport and regulation of striated muscle contraction. Predicted to act upstream of or within positive regulation of ATPase-coupled calcium transmembrane transporter activity and positive regulation of calcium ion import. Predicted to be located in sarcoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Mar 2025]

SCYGR6 Gene

small cysteine and glycine repeat containing 6

Predicted to be located in intermediate filament. [provided by Alliance of Genome Resources, Mar 2025]

SMIM42 Gene

small integral membrane protein 42

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM47 Gene

small integral membrane protein 47

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SMIM32 Gene

small integral membrane protein 32

Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025]

SCYGR10 Gene

small cysteine and glycine repeat containing 10 (gene/pseudogene)

This gene is a member of a large gene family that encodes keratin associated proteins (KRTAP) that play a role in hair formation. This gene belongs to a subfamily of the KRTAP family termed small cysteine and glycine repeat containing (SCYGR) genes and it resides in a cluster of SCYGR genes on chromosome 2q36.3. Allelic polymorphisms in this gene result in both coding and non-coding transcripts; the reference genome represents the non-coding allele. [provided by RefSeq, Jan 2024]

FSAF1 Gene

40S small subunit processome assembly factor 1

Enables RNA binding activity. Involved in ribosomal small subunit biogenesis. Located in chromosome. Part of small-subunit processome. [provided by Alliance of Genome Resources, Mar 2025]

SCYGR1 Gene

small cysteine and glycine repeat containing 1

SCYGR7 Gene

small cysteine and glycine repeat containing 7

SCYGR8 Gene

small cysteine and glycine repeat containing 8

SCYGR3 Gene

small cysteine and glycine repeat containing 3

SCYGR2 Gene

small cysteine and glycine repeat containing 2

SCYGR5 Gene

small cysteine and glycine repeat containing 5

LOC107983987 Gene

small integral membrane protein 34B

SMIM39 Gene

small integral membrane protein 39

SMIM10L3 Gene

small integral membrane protein 10 like 3

SMIM46 Gene

small integral membrane protein 46

multiple small vertebral fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple small vertebral fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fractures, bone; hip fractures; proximal humeral fractures; shoulder fractures; wrist injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; hip fractures; proximal humeral fractures; shoulder fractures; wrist injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

[Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7 <small>Dsmall>-Tic9]OT Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7 <small>Dsmall>-Tic9]OT ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

fractures, spontaneous; hip fractures; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; hip fractures; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

femoral neck fractures; fractures, bone; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease femoral neck fractures; fractures, bone; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; fractures, closed; humeral fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; fractures, closed; humeral fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Cha-<small>Dsmall>-Arg-CO2H Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Cha-<small>Dsmall>-Arg-CO2H ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7]OT Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7]OT ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7 Aib9]OT Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7 Aib9]OT ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Trp-<small>Dsmall>-Arg-CO2H Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Trp-<small>Dsmall>-Arg-CO2H ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

fractures, spontaneous; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; osteoporosis; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, spontaneous; osteoporosis; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

femoral neck fractures; fractures, stress Gene Set

From GAD Gene-Disease Associations

genes associated with the disease femoral neck fractures; fractures, stress in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; lactose intolerance; osteoporosis; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; lactose intolerance; osteoporosis; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cushing syndrome; fractures, bone; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cushing syndrome; fractures, bone; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; hip fractures; osteoporosis; spinal injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; hip fractures; osteoporosis; spinal injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; osteoporotic fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; osteoporotic fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; fractures, bone; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; fractures, bone; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; fractures, vertebral Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; fractures, vertebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

prevalent vertebral fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease prevalent vertebral fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vertebral compression fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral compression fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Fractures (vertebral) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Fractures (vertebral) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

multiple prenatal fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple prenatal fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bowing of limbs due to multiple fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the bowing of limbs due to multiple fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple rib fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple rib fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Multiple Prenatal Fractures Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Prenatal Fractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Bowing Of Limbs Due To Multiple Fractures Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Bowing Of Limbs Due To Multiple Fractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung ; radiation pneumonitis; small cell carcinoma of lung; small cell lung carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung ; radiation pneumonitis; small cell carcinoma of lung; small cell lung carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

small cervical vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the small cervical vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

small vertebral body Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small vertebral body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Small Cervical Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Small Cervical Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

small vertebral body Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the small vertebral body phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis, chronic progressive; multiple sclerosis, relapsing-remitting; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; multiple trauma; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; multiple trauma; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Multiple synapse bouton, contacting multiple dendrites Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Multiple synapse bouton, contacting multiple dendrites cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

multiple small medullary renal cysts Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple small medullary renal cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Multiple Small Medullary Renal Cysts Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Small Medullary Renal Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma, large cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma, large cell; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

paraneoplastic syndromes, nervous system; small cell carcinoma of lung; small cell lung carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease paraneoplastic syndromes, nervous system; small cell carcinoma of lung; small cell lung carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

d(CH2)5[<small>Dsmall>-Ile2 Val4 Tyr-NH29]AVP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the d(CH2)5[<small>Dsmall>-Ile2 Val4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

d[<small>Dsmall>-Phe2]AVP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the d[<small>Dsmall>-Phe2]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[125I]d(CH2)5[<small>Dsmall>-Ile2 Ile4 Tyr-NH29]AVP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [125I]d(CH2)5[<small>Dsmall>-Ile2 Ile4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[Phaa1 <small>Dsmall>-Tyr2 Val4 Arg6 Arg-NH29]AVP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [Phaa1 <small>Dsmall>-Tyr2 Val4 Arg6 Arg-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[<small>Dsmall>-Bpa5 Ile13]motilin (human) Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [<small>Dsmall>-Bpa5 Ile13]motilin (human) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[tBaa1 <small>Dsmall>-Tyr(Et)2 Val4 Lys6 Arg-NH28 des-Gly9]AVP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [tBaa1 <small>Dsmall>-Tyr(Et)2 Val4 Lys6 Arg-NH28 des-Gly9]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

d(CH2)5[<small>Dsmall>-Ile2 Ile4 Tyr-NH29]AVP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the d(CH2)5[<small>Dsmall>-Ile2 Ile4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

d(CH2)5[<small>Dsmall>-Ile2 Ile4 Ala-NH29]AVP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the d(CH2)5[<small>Dsmall>-Ile2 Ile4 Ala-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[His5 <small>Dsmall>-Tyr6]GnRH Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [His5 <small>Dsmall>-Tyr6]GnRH ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[125I]d(CH2)5[<small>Dsmall>-Tyr(Et)2 Val4 Tyr-NH29]AVP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [125I]d(CH2)5[<small>Dsmall>-Tyr(Et)2 Val4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

d(CH2)5[<small>Dsmall>-Ile2 Ile4]AVP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the d(CH2)5[<small>Dsmall>-Ile2 Ile4]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[<small>Lsmall>-Bpa5 Ile13]motilin (human) Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [<small>Lsmall>-Bpa5 Ile13]motilin (human) ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[des-Gly10 <small>Dsmall>-Ala6]GnRH N-ethylamide Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [des-Gly10 <small>Dsmall>-Ala6]GnRH N-ethylamide ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[Phaa1 <small>Dsmall>-Tyr(Et)2 Val4 Lys6 Tyr-NH28 des-Gly9]AVP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [Phaa1 <small>Dsmall>-Tyr(Et)2 Val4 Lys6 Tyr-NH28 des-Gly9]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[Sar <small>Dsmall>-Phe8 des-Arg9]bradykinin Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [Sar <small>Dsmall>-Phe8 des-Arg9]bradykinin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

d[<small>Dsmall>-Pal2]AVP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the d[<small>Dsmall>-Pal2]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

d(CH2)5[<small>Dsmall>-Tyr(Et)2 Val4 Tyr-NH29]AVP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the d(CH2)5[<small>Dsmall>-Tyr(Et)2 Val4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

d(CH2)5[<small>Dsmall>-Ile2 Ile4 Ala-NH2]AVP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the d(CH2)5[<small>Dsmall>-Ile2 Ile4 Ala-NH2]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[Phaa1 <small>Dsmall>-Tyr(Me)2 Arg6 Tyr-NH29]AVP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [Phaa1 <small>Dsmall>-Tyr(Me)2 Arg6 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[125I]d(CH2)5[<small>Dsmall>-Tyr(Et)2 Ile4 Tyr-NH29]AVP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [125I]d(CH2)5[<small>Dsmall>-Tyr(Et)2 Ile4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[<small>Dsmall>-Lys1 des-Arg10]kallidin Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [<small>Dsmall>-Lys1 des-Arg10]kallidin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[125I]d(CH2)5[<small>Dsmall>-Ile2 Val4 Tyr-NH29]AVP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [125I]d(CH2)5[<small>Dsmall>-Ile2 Val4 Tyr-NH29]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

<small>Dsmall>-Lys0-[des-Arg10]kallidin Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the <small>Dsmall>-Lys0-[des-Arg10]kallidin ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[Phaa1 <small>Dsmall>-Tyr(Et)2 Lys6 des-Gly9]AVP Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [Phaa1 <small>Dsmall>-Tyr(Et)2 Lys6 des-Gly9]AVP ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

[125I][des-Gly10 <small>Dsmall>-Ala6]GnRH N-ethylamide Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the [125I][des-Gly10 <small>Dsmall>-Ala6]GnRH N-ethylamide ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

U1 small nuclear ribonucleoprotein A/U2 small nuclear ribonucleoprotein B'' Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the U1 small nuclear ribonucleoprotein A/U2 small nuclear ribonucleoprotein B'' protein domain from the InterPro Predicted Protein Domain Annotations dataset.

non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease non-small cell large cell lung carcinoma; non-small cell squamous cell lung carcinoma from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Femoral Fractures Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Femoral Fractures from the curated CTD Gene-Disease Associations dataset.

Fractures, Bone Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fractures, Bone from the curated CTD Gene-Disease Associations dataset.

Hip Fractures Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hip Fractures from the curated CTD Gene-Disease Associations dataset.

Fractures, Closed Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fractures, Closed from the curated CTD Gene-Disease Associations dataset.

bone resorption; fractures, bone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone resorption; fractures, bone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced risk of osteoporotic fractures case control study Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced risk of osteoporotic fractures case control study in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; rett syndrome; scoliosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; rett syndrome; scoliosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acromegaly; cardiovascular diseases; colonic diseases; osteoarthritis; osteoporosis; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acromegaly; cardiovascular diseases; colonic diseases; osteoarthritis; osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid deficiency; fractures, bone; osteoporosis, postmenopausal; riboflavin deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain edema; brain injuries; cerebral hemorrhage, traumatic; skull fractures; traumatic cerebral hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain edema; brain injuries; cerebral hemorrhage, traumatic; skull fractures; traumatic cerebral hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoporotic fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoporotic fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hip fractures; osteoporosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hip fractures; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

prevalent fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease prevalent fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; fractures, bone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; fractures, bone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; osteoporosis, postmenopausal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoporotic fractures but polymorphisms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoporotic fractures but polymorphisms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, stress Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, stress in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; rett syndrome; seizures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; rett syndrome; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; osteoarthritis; osteoarthritis, knee Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; osteoarthritis; osteoarthritis, knee in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

degenerative arthropathy ; hip fractures; osteoarthritis; osteoarthritis, hip; osteoarthritis, knee; osteoporosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease degenerative arthropathy ; hip fractures; osteoarthritis; osteoarthritis, hip; osteoarthritis, knee; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hip fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hip fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; osteoporosis; osteoporosis, postmenopausal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; osteoporosis; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoporosis; osteoporosis, postmenopausal; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoporosis; osteoporosis, postmenopausal; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

femoral neck fractures; osteoporosis; spinal injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease femoral neck fractures; osteoporosis; spinal injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; fractures; osteocalcin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; fractures; osteocalcin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; calcium; fractures, nonvertebral; milk intolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; calcium; fractures, nonvertebral; milk intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hip fractures; osteoporosis, postmenopausal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hip fractures; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoporosis, postmenopausal; radius fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoporosis, postmenopausal; radius fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoporosis; spinal fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoporosis; spinal fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; colles' fracture; fractures, spontaneous; osteoporosis, postmenopausal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; colles' fracture; fractures, spontaneous; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hip fractures; osteoarthritis, hip Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hip fractures; osteoarthritis, hip in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone mass; osteoporotic fractures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone mass; osteoporotic fractures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenoma; adrenal gland neoplasms; adrenal neoplasm; diabetes mellitus; dyslipidemias; fractures, bone; hypertension; osteoporosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenoma; adrenal gland neoplasms; adrenal neoplasm; diabetes mellitus; dyslipidemias; fractures, bone; hypertension; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pain, postoperative; radius fractures; reflex sympathetic dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pain, postoperative; radius fractures; reflex sympathetic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, spontaneous; osteoporosis, postmenopausal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, spontaneous; osteoporosis, postmenopausal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; cardiovascular diseases; genital neoplasms, female; hip fractures; mammary neoplasms; neoplasms; neoplasms, prostatic; prostatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; cardiovascular diseases; genital neoplasms, female; hip fractures; mammary neoplasms; neoplasms; neoplasms, prostatic; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures, bone; osteoporosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fractures, bone; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fractures Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term fractures in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

fractures of the long bones Gene Set

From HPO Gene-Disease Associations

genes associated with the fractures of the long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

recurrent fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteomyelitis leading to amputation due to slow healing fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the osteomyelitis leading to amputation due to slow healing fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized osteoporosis with pathologic fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized osteoporosis with pathologic fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased susceptibility to fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the increased susceptibility to fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

painless fractures due to injury Gene Set

From HPO Gene-Disease Associations

genes associated with the painless fractures due to injury phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Tibial Fractures Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Tibial Fractures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Femoral Neck Fractures Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Femoral Neck Fractures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Fractures, Ununited Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Fractures, Ununited phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Femoral Fractures Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Femoral Fractures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Fractures, Spontaneous Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Fractures, Spontaneous phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Shoulder Fractures Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Shoulder Fractures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Fractures, Bone Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Fractures, Bone phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Humeral Fractures Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Humeral Fractures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hip Fractures Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hip Fractures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Fractures, Closed Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Fractures, Closed phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ulna Fractures Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ulna Fractures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Skull Fractures Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Skull Fractures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Radius Fractures Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Radius Fractures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Spinal Fractures Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Spinal Fractures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Fractures, Stress Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Fractures, Stress phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Fractures, Compression Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Fractures, Compression phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Osteoporotic Fractures Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Osteoporotic Fractures phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

rib fractures Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the rib fractures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures phenotype from the curated OMIM Gene-Disease Associations dataset.

Pseudo-Fractures Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Pseudo-Fractures in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Increased Susceptibility To Fractures Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Increased Susceptibility To Fractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Osteomyelitis Leading To Amputation Due To Slow Healing Fractures Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Osteomyelitis Leading To Amputation Due To Slow Healing Fractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Fractures Of The Long Bones Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Fractures Of The Long Bones in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Painless Fractures Due To Injury Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Painless Fractures Due To Injury in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

rib fractures Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the rib fractures phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Increased susceptibility to fractures Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Increased susceptibility to fractures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Fractures (paediatric) Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Fractures (paediatric) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Fractures Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Fractures phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Nonunion in individuals with fractures Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Nonunion in individuals with fractures phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Sacral agenesis with vertebral anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sacral agenesis with vertebral anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

vertebral artery insufficiency Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease vertebral artery insufficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

vertebral artery occlusion Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease vertebral artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

vertebral artery dissection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vertebral artery dissection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; brain ischemia; carotid artery, internal, dissection; hyperhomocysteinemia; stroke; vertebral artery dissection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; brain ischemia; carotid artery, internal, dissection; hyperhomocysteinemia; stroke; vertebral artery dissection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vertebral fracture Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vertebral fracture in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vertebral Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term vertebral in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

abnormality of the vertebral column Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

vertebral body sclerosis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the vertebral body sclerosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the curvature of the vertebral column Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the curvature of the vertebral column phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

butterfly vertebral arch Gene Set

From HPO Gene-Disease Associations

genes associated with the butterfly vertebral arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sclerotic vertebral endplates Gene Set

From HPO Gene-Disease Associations

genes associated with the sclerotic vertebral endplates phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cervical vertebral fusion (c2/c3) Gene Set

From HPO Gene-Disease Associations

genes associated with the cervical vertebral fusion (c2/c3) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent or minimally ossified vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the absent or minimally ossified vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

posterior vertebral hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the posterior vertebral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral segmentation defect Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral segmentation defect phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral hyperostosis Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral hyperostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

narrow vertebral interpedicular distance Gene Set

From HPO Gene-Disease Associations

genes associated with the narrow vertebral interpedicular distance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral arch anomaly Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral arch anomaly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cleft vertebral arch Gene Set

From HPO Gene-Disease Associations

genes associated with the cleft vertebral arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

c1-c2 vertebral abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the c1-c2 vertebral abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal vertebral pedicle morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal vertebral pedicle morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cuboid-shaped vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the cuboid-shaped vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior clefting of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior clefting of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

biconcave vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the biconcave vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

irregular vertebral endplates Gene Set

From HPO Gene-Disease Associations

genes associated with the irregular vertebral endplates phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral body sclerosis Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral body sclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

beaking of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the beaking of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

tall lumbar vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the tall lumbar vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia involving the vertebral column Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia involving the vertebral column phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal vertebral segmentation and fusion Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal vertebral segmentation and fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

beaking of vertebral bodies t12-l3 Gene Set

From HPO Gene-Disease Associations

genes associated with the beaking of vertebral bodies t12-l3 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral clefting Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral clefting phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the curvature of the vertebral column Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the curvature of the vertebral column phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sandwich appearance of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the sandwich appearance of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal form of the vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal form of the vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

enlarged vertebral pedicles Gene Set

From HPO Gene-Disease Associations

genes associated with the enlarged vertebral pedicles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

posterior scalloping of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the posterior scalloping of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

posterior wedging of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the posterior wedging of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypoplastic vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the hypoplastic vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral fusion Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal vertebral ossification Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal vertebral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the vertebral spinous processes Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the vertebral spinous processes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent in utero ossification of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the absent in utero ossification of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

disc-like vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the disc-like vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent vertebral body mineralization Gene Set

From HPO Gene-Disease Associations

genes associated with the absent vertebral body mineralization phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

unossified vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the unossified vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior rounding of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior rounding of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

supernumerary vertebral ossification centers Gene Set

From HPO Gene-Disease Associations

genes associated with the supernumerary vertebral ossification centers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the vertebral endplates Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the vertebral endplates phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased vertebral height Gene Set

From HPO Gene-Disease Associations

genes associated with the increased vertebral height phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ovoid vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the ovoid vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

vertebral wedging Gene Set

From HPO Gene-Disease Associations

genes associated with the vertebral wedging phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hump-shaped mound of bone in central and posterior portions of vertebral endplate Gene Set

From HPO Gene-Disease Associations

genes associated with the hump-shaped mound of bone in central and posterior portions of vertebral endplate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive cervical vertebral spine fusion Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive cervical vertebral spine fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of vertebral epiphysis morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of vertebral epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

scheuermann-like vertebral changes Gene Set

From HPO Gene-Disease Associations

genes associated with the scheuermann-like vertebral changes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

punctate vertebral calcifications Gene Set

From HPO Gene-Disease Associations

genes associated with the punctate vertebral calcifications phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the vertebral column Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the vertebral column phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Vertebral Artery Dissection Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Vertebral Artery Dissection phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

asymmetric rib-vertebral column attachment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the asymmetric rib-vertebral column attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral lamina morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral lamina morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral arch morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

caudal vertebral transformation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the caudal vertebral transformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

vertebral transformation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vertebral transformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

fusion of vertebral arches Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the fusion of vertebral arches phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cervical vertebral transformation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cervical vertebral transformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vertebral spinous process Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vertebral spinous process phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short vertebral body Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short vertebral body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

lumbar vertebral fusion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the lumbar vertebral fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral pedicle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral pedicle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vertebral arch Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vertebral arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral artery morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral artery morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral articular process morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral articular process morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thoracic vertebral fusion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thoracic vertebral fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sacral vertebral transformation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the sacral vertebral transformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral column morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vertebral body Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vertebral body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral epiphyseal plate morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral epiphyseal plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged vertebral body Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged vertebral body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral spinous process morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral spinous process morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vertebral pedicles Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vertebral pedicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cervical vertebral fusion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the cervical vertebral fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

vertebral compression Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vertebral compression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

fusion of vertebral bodies Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the fusion of vertebral bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

elongated vertebral body Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the elongated vertebral body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

vertebral fusion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vertebral fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

vertebral body hypoplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the vertebral body hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal rib-vertebral column attachment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal rib-vertebral column attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral arch development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral arch development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vertebral transverse processes Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vertebral transverse processes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sacral vertebral fusion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the sacral vertebral fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

lumbar vertebral transformation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the lumbar vertebral transformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

caudal vertebral fusion Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the caudal vertebral fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short vertebral column Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short vertebral column phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thoracic vertebral transformation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thoracic vertebral transformation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral body morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral body morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

elongated vertebral column Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the elongated vertebral column phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral body development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral body development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vertebral transverse process morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal vertebral transverse process morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sacral agenesis with vertebral anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the sacral agenesis with vertebral anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

vertebral ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue vertebral ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Vertebral Chordoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Vertebral Chordoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Secondary Malignant Neoplasm Of Vertebral Column Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Secondary Malignant Neoplasm Of Vertebral Column in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Defect Of Vertebral Segmentation Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Defect Of Vertebral Segmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Abnormal Vertebral Segmentation And Fusion Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Abnormal Vertebral Segmentation And Fusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Vertebral Osteoporosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Vertebral Osteoporosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Abnormality Of The Vertebral Spinous Processes Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Abnormality Of The Vertebral Spinous Processes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Abnormality Of The Vertebral Endplates Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Abnormality Of The Vertebral Endplates in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Abnormality Of Vertebral Epiphysis Morphology Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Abnormality Of Vertebral Epiphysis Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Vertebral Artery Dissection Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Vertebral Artery Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Vertebral Artery Aneurysm Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Vertebral Artery Aneurysm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Punctate Vertebral Calcifications Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Punctate Vertebral Calcifications in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Vertebral Wedging Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Vertebral Wedging in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Vertebral Body Haemangioma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Vertebral Body Haemangioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Vertebral Lesion Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Vertebral Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Vertebral, Cardiac, Renal, And Limb Defects Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Vertebral, Cardiac, Renal, And Limb Defects Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Supernumerary Vertebral Ossification Centers Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Supernumerary Vertebral Ossification Centers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Vertebral Artery Hypoplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Vertebral Artery Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Cervical Vertebral Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Cervical Vertebral Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

C1-C2 Vertebral Abnormality Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease C1-C2 Vertebral Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Enlarged Vertebral Pedicles Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Enlarged Vertebral Pedicles in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Vertebral Anomalies Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Vertebral Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Sacral Agenesis With Vertebral Anomalies Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Sacral Agenesis With Vertebral Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Cuboid-Shaped Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Cuboid-Shaped Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Ovoid Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Ovoid Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormal Form Of The Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormal Form Of The Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Irregular Vertebral Endplates Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Irregular Vertebral Endplates in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormal Vertebral Morphology Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormal Vertebral Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Progressive Cervical Vertebral Spine Fusion Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Progressive Cervical Vertebral Spine Fusion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Beaking Of Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Beaking Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Biconcave Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Biconcave Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Compression Fracture Of Vertebral Column Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Compression Fracture Of Vertebral Column in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Unossified Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Unossified Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Vertebral Clefting Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Vertebral Clefting in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Abnormality Of The Vertebral Column Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Abnormality Of The Vertebral Column in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Vertebral Arch Anomaly Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Vertebral Arch Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Absent In Utero Ossification Of Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Absent In Utero Ossification Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Absent Or Minimally Ossified Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Absent Or Minimally Ossified Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Increased Vertebral Height Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Increased Vertebral Height in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Sclerotic Vertebral Endplates Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Sclerotic Vertebral Endplates in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Anterior Clefting Of Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Anterior Clefting Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Narrow Vertebral Interpedicular Distance Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Narrow Vertebral Interpedicular Distance in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Sandwich Appearance Of Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Sandwich Appearance Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Irregularity Of Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Irregularity Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Posterior Vertebral Hypoplasia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Posterior Vertebral Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Absent Vertebral Body Mineralization Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Absent Vertebral Body Mineralization in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Disc-Like Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Disc-Like Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Central Vertebral Hypoplasia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Central Vertebral Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Hyperconvex Vertebral Body Endplates Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Hyperconvex Vertebral Body Endplates in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Cervical C3/C4 Vertebral Fusion Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Cervical C3/C4 Vertebral Fusion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Vertebral Hyperostosis Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Vertebral Hyperostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Unilateral Vertebral Artery Hypoplasia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Unilateral Vertebral Artery Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Butterfly Vertebral Arch Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Butterfly Vertebral Arch in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Posterior Scalloping Of Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Posterior Scalloping Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Sclerotic Vertebral Body Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Sclerotic Vertebral Body in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Tall Lumbar Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Tall Lumbar Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Scheuermann-Like Vertebral Changes Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Scheuermann-Like Vertebral Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Modic Type Vertebral Endplate Changes Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Modic Type Vertebral Endplate Changes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Posterior Wedging Of Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Posterior Wedging Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Anterior Rounding Of Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Anterior Rounding Of Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Hump-Shaped Mound Of Bone In Central And Posterior Portions Of Vertebral Endplate Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Hump-Shaped Mound Of Bone In Central And Posterior Portions Of Vertebral Endplate in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Biconvex Vertebral Bodies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Biconvex Vertebral Bodies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

abnormal vertebral arch morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal vertebral arch morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

cervical vertebral transformation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the cervical vertebral transformation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

absent vertebral body Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the absent vertebral body phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal vertebral body morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal vertebral body morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

short vertebral body Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the short vertebral body phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

fusion of vertebral arches Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the fusion of vertebral arches phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal vertebral artery morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal vertebral artery morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal vertebral body development Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal vertebral body development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

short vertebral column Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the short vertebral column phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

sacral vertebral transformation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the sacral vertebral transformation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

thoracic vertebral transformation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the thoracic vertebral transformation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

vertebral fusion Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the vertebral fusion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

caudal vertebral fusion Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the caudal vertebral fusion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

absent vertebral pedicles Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the absent vertebral pedicles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

absent vertebral transverse processes Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the absent vertebral transverse processes phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

fusion of vertebral bodies Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the fusion of vertebral bodies phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal vertebral lamina morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal vertebral lamina morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal vertebral column morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal vertebral column morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

cervical vertebral fusion Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the cervical vertebral fusion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

lumbar vertebral fusion Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the lumbar vertebral fusion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

sacral vertebral fusion Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the sacral vertebral fusion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

caudal vertebral transformation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the caudal vertebral transformation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal vertebral arch development Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal vertebral arch development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

vertebral compression Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the vertebral compression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

vertebral transformation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the vertebral transformation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal vertebral spinous process morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal vertebral spinous process morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

lumbar vertebral transformation Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the lumbar vertebral transformation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal vertebral transverse process morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal vertebral transverse process morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

enlarged vertebral body Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the enlarged vertebral body phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal vertebral pedicle morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal vertebral pedicle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal vertebral epiphyseal plate morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal vertebral epiphyseal plate morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

thoracic vertebral fusion Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the thoracic vertebral fusion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

absent vertebral arch Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the absent vertebral arch phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

vertebral body hypoplasia Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the vertebral body hypoplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

elongated vertebral body Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the elongated vertebral body phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal vertebral articular process morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal vertebral articular process morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

elongated vertebral column Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the elongated vertebral column phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

absent vertebral spinous process Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the absent vertebral spinous process phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal vertebral artery topology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal vertebral artery topology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

additional anastomosis between intracranial vertebral arteries Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the additional anastomosis between intracranial vertebral arteries phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

anastomosis between common carotid and vertebral artery Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the anastomosis between common carotid and vertebral artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

absent extracranial vertebral artery segment Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the absent extracranial vertebral artery segment phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

absent intracranial segment of vertebral artery Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the absent intracranial segment of vertebral artery phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal vertebral artery origin Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal vertebral artery origin phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

vertebral transformation Gene Set

From IMPC Knockout Mouse Phenotypes

gene knockouts causing the vertebral transformation phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.

abnormal vertebral arch morphology Gene Set

From IMPC Knockout Mouse Phenotypes

gene knockouts causing the abnormal vertebral arch morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.

vertebral fusion Gene Set

From IMPC Knockout Mouse Phenotypes

gene knockouts causing the vertebral fusion phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.

fusion of vertebral arches Gene Set

From IMPC Knockout Mouse Phenotypes

gene knockouts causing the fusion of vertebral arches phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.

Vertebral hypersegmentation and orofacial anomalies Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Vertebral hypersegmentation and orofacial anomalies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Vertebral artery occlusion Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Vertebral artery occlusion in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Vertebral artery insufficiency Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Vertebral artery insufficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Vertebral anomalies and variable endocrine and T-cell dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Vertebral endplate Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Vertebral endplate in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Vertebral ganglion Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Vertebral ganglion in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Vertebral anomalies and variable endocrine and T-cell dysfunction Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Vertebral anomalies and variable endocrine and T-cell dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Absent vertebral body mineralization Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Absent vertebral body mineralization phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Vertebral Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Vertebral phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Tricho-oculo-dermo-vertebral syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Tricho-oculo-dermo-vertebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Abnormality of the vertebral column Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Abnormality of the vertebral column phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

multiple antiapoptotic pathways from igf-1r signaling lead to bad phosphorylation Gene Set

From Biocarta Pathways

proteins participating in the multiple antiapoptotic pathways from igf-1r signaling lead to bad phosphorylation pathway from the Biocarta Pathways dataset.

CUX1-19635798-MULTIPLE HUMAN CANCER CELL TYPES-HUMAN Gene Set

From ChEA Transcription Factor Binding Site Profiles

genes with transcription factor binding evidence in the CUX1-19635798-MULTIPLE HUMAN CANCER CELL TYPES-HUMAN transcription factor binding site profile from the CHEA Transcription Factor Binding Site Profiles dataset.

Multiple synostoses syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple synostoses syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epiphyseal dysplasia, multiple, 3, with myopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epiphyseal dysplasia, multiple, 3, with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract 15, multiple types Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract 15, multiple types phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, autosomal dominant, multiple types, with microcornea Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, autosomal dominant, multiple types, with microcornea phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lethal multiple pterygium syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple Cutaneous and Mucosal Venous Malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple Cutaneous and Mucosal Venous Malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepimetaphyseal dysplasia with multiple dislocations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepimetaphyseal dysplasia with multiple dislocations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple endocrine neoplasia, type 2b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple endocrine neoplasia, type 2b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple fibrofolliculomas Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple fibrofolliculomas phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple sulfatase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple synostoses syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple synostoses syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple pterygium syndrome Escobar type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple pterygium syndrome Escobar type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital heart disease, multiple types, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital heart defects, multiple types, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital heart defects, multiple types, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MEN2 phenotype: Unknown:Multiple endocrine neoplasia, type 2a Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the MEN2 phenotype: Unknown:Multiple endocrine neoplasia, type 2a phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple gastrointestinal atresias Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple gastrointestinal atresias phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple exostoses type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple exostoses type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple endocrine neoplasia, type 2a Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple endocrine neoplasia, type 2a phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple mitochondrial dysfunctions syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple mitochondrial dysfunctions syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple mitochondrial dysfunctions syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple mitochondrial dysfunctions syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Familial multiple polyposis syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple endocrine neoplasia, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple endocrine neoplasia, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital exostosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital exostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple epiphyseal dysplasia 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple epiphyseal dysplasia 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple epiphyseal dysplasia 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple epiphyseal dysplasia 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple epiphyseal dysplasia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple epiphyseal dysplasia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple fibroadenomas of the breast Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple fibroadenomas of the breast phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

LIPOMATOSIS, MULTIPLE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease LIPOMATOSIS, MULTIPLE from the curated CTD Gene-Disease Associations dataset.

Multiple Endocrine Neoplasia Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 1 from the curated CTD Gene-Disease Associations dataset.

Cafe au lait spots, multiple Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cafe au lait spots, multiple from the curated CTD Gene-Disease Associations dataset.

Multiple Organ Failure Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Organ Failure from the curated CTD Gene-Disease Associations dataset.

EXOSTOSES, MULTIPLE, TYPE II Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EXOSTOSES, MULTIPLE, TYPE II from the curated CTD Gene-Disease Associations dataset.

Multiple Endocrine Neoplasia Type 2a Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 2a from the curated CTD Gene-Disease Associations dataset.

Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset.

Multiple Myeloma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Myeloma from the curated CTD Gene-Disease Associations dataset.

Venous Malformations, Multiple Cutaneous and Mucosal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Venous Malformations, Multiple Cutaneous and Mucosal from the curated CTD Gene-Disease Associations dataset.

MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE from the curated CTD Gene-Disease Associations dataset.

Multiple Synostoses Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Synostoses Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

CATARACT 32, MULTIPLE TYPES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CATARACT 32, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.

Exostoses, Multiple Hereditary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Exostoses, Multiple Hereditary from the curated CTD Gene-Disease Associations dataset.

Hamartoma Syndrome, Multiple Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hamartoma Syndrome, Multiple from the curated CTD Gene-Disease Associations dataset.

VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 from the curated CTD Gene-Disease Associations dataset.

Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Acyl Coenzyme A Dehydrogenase Deficiency from the curated CTD Gene-Disease Associations dataset.

CATARACT 6, MULTIPLE TYPES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CATARACT 6, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.

Multiple Endocrine Neoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Endocrine Neoplasia from the curated CTD Gene-Disease Associations dataset.

Exostoses, Multiple, Type III Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Exostoses, Multiple, Type III from the curated CTD Gene-Disease Associations dataset.

Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency from the curated CTD Gene-Disease Associations dataset.

Multiple Sclerosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Sclerosis from the curated CTD Gene-Disease Associations dataset.

Multiple Chemical Sensitivity Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Chemical Sensitivity from the curated CTD Gene-Disease Associations dataset.

Multiple synostoses syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple synostoses syndrome 2 from the curated CTD Gene-Disease Associations dataset.

Multiple Sclerosis, Relapsing-Remitting Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Sclerosis, Relapsing-Remitting from the curated CTD Gene-Disease Associations dataset.

Multiple Endocrine Neoplasia Type 2b Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Endocrine Neoplasia Type 2b from the curated CTD Gene-Disease Associations dataset.

MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.

Cataract, Autosomal Dominant, Multiple Types 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Autosomal Dominant, Multiple Types 1 from the curated CTD Gene-Disease Associations dataset.

Trichoepithelioma multiple familial Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Trichoepithelioma multiple familial from the curated CTD Gene-Disease Associations dataset.

Multiple pterygium syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple pterygium syndrome from the curated CTD Gene-Disease Associations dataset.

Abnormalities, Multiple Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Abnormalities, Multiple from the curated CTD Gene-Disease Associations dataset.

Multiple Endocrine Neoplasia, Type IV Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Endocrine Neoplasia, Type IV from the curated CTD Gene-Disease Associations dataset.

VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 from the curated CTD Gene-Disease Associations dataset.

CATARACT 3, MULTIPLE TYPES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CATARACT 3, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.

Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies from the curated CTD Gene-Disease Associations dataset.

EXOSTOSES, MULTIPLE, TYPE I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease EXOSTOSES, MULTIPLE, TYPE I from the curated CTD Gene-Disease Associations dataset.

CATARACT 4, MULTIPLE TYPES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CATARACT 4, MULTIPLE TYPES from the curated CTD Gene-Disease Associations dataset.

Multiple Sulfatase Deficiency Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multiple Sulfatase Deficiency Disease from the curated CTD Gene-Disease Associations dataset.

MULTIPLE SYNOSTOSES SYNDROME 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MULTIPLE SYNOSTOSES SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.

Trichoepithelioma, Multiple Familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Trichoepithelioma, Multiple Familial, 2 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 1 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 3 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 2 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 5 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 4 from the curated CTD Gene-Disease Associations dataset.

Multiple Sclerosis Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Multiple Sclerosis in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Multiple Myeloma Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Multiple Myeloma in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

multiple system atrophy Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease multiple system atrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

hereditary multiple exostoses Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease hereditary multiple exostoses from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

multiple epiphyseal dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease multiple epiphyseal dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

multiple sclerosis Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease multiple sclerosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

multiple carboxylase deficiency Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease multiple carboxylase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

multiple myeloma Gene Set

From DISEASES Experimental Gene-Disease Association Evidence Scores

genes associated with the disease multiple myeloma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

multiple sclerosis Gene Set

From DISEASES Experimental Gene-Disease Association Evidence Scores

genes associated with the disease multiple sclerosis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

multiple intestinal atresia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease multiple intestinal atresia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

multiple myeloma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease multiple myeloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

hereditary multiple exostoses Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease hereditary multiple exostoses in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

multiple mucosal neuroma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease multiple mucosal neuroma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

multiple chemical sensitivity Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease multiple chemical sensitivity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

multiple symmetrical lipomatosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease multiple symmetrical lipomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

multiple epiphyseal dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease multiple epiphyseal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

multiple carboxylase deficiency Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease multiple carboxylase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

multiple symmetric lipomatosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease multiple symmetric lipomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

multiple cranial nerve palsy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease multiple cranial nerve palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

multiple personality disorder Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease multiple personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

multiple system atrophy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

relapsing-remitting multiple sclerosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease relapsing-remitting multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

multiple sclerosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

critical illness; multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease critical illness; multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis; lupus erythematosus; wegener's granulomatosis; guillain-barre syndrome; thrombocytopenic purpura, idiopathic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis; lupus erythematosus; wegener's granulomatosis; guillain-barre syndrome; thrombocytopenic purpura, idiopathic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; neoplasms, multiple primary; nevus; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; neoplasms, multiple primary; nevus; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis; optic neuritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis; optic neuritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; craniofacial abnormalities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; craniofacial abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; diabetes mellitus, type 1; inflammatory bowel diseases; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; diabetes mellitus, type 1; inflammatory bowel diseases; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; sepsis; shock, septic; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; sepsis; shock, septic; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; pancreatitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; pancreatitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; sepsis; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; sepsis; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; arrhythmias, cardiac; autonomic nervous system diseases; death, sudden; hypoventilation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple epiphyseal dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple epiphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

burns; multiple organ failure; shock Gene Set

From GAD Gene-Disease Associations

genes associated with the disease burns; multiple organ failure; shock in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; multiple myeloma; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; multiple myeloma; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune thyroiditis; breast neoplasms; mammary neoplasms; multiple sclerosis; rheumatoid spondylitis; spondylitis, ankylosing; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune thyroiditis; breast neoplasms; mammary neoplasms; multiple sclerosis; rheumatoid spondylitis; spondylitis, ankylosing; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis (age of onset) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis (age of onset) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis; diabetes, type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis; diabetes, type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of muscle, unspec; lipidoses; lipoidosis; multiple acyl coenzyme a dehydrogenase deficiency; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis; crohn's disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis; crohn's disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; multiple sclerosis; hiv Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; multiple sclerosis; hiv in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; multiple myeloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myelogenous, chronic, bcr-abl positive; leukemia, myeloid, acute; leukemias, acute myeloblastic; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone diseases, metabolic; gaucher disease; hypergammaglobulinemia; multiple myeloma; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone diseases, metabolic; gaucher disease; hypergammaglobulinemia; multiple myeloma; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; respiratory distress syndrome, adult; sepsis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; respiratory distress syndrome, adult; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hodgkin's disease leukemia, myeloid multiple myeloma myelodysplastic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hodgkin's disease leukemia, myeloid multiple myeloma myelodysplastic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

susceptibility to multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease susceptibility to multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

genetic predisposition to disease; multiple myeloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease genetic predisposition to disease; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; autoimmune diseases; diabetes mellitus, type 1; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic lymphocytic leukemia; hodgkin disease; leukemia, lymphocytic, chronic, b-cell; multiple myeloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic lymphocytic leukemia; hodgkin disease; leukemia, lymphocytic, chronic, b-cell; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; craniofacial abnormalities; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; craniofacial abnormalities; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

learning disorders; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease learning disorders; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis; lupus erythematosus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis; lupus erythematosus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple myeloma; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple myeloma; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis; diabetes, gestational; insulin; diabetes, type 1; rhinitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis; diabetes, gestational; insulin; diabetes, type 1; rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hamartoma syndrome, multiple Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hamartoma syndrome, multiple in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple myeloma; myelodysplastic syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple myeloma; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple myeloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apoplexy; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; multiple sclerosis; stroke Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apoplexy; diabetes mellitus, insulin-dependent; diabetes mellitus, type 1; multiple sclerosis; stroke in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, myeloid, acute; lymphoma, non-hodgkin; multiple myeloma; myelodysplastic syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms, multiple primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

jaw diseases; multiple myeloma; osteonecrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease jaw diseases; multiple myeloma; osteonecrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal gland neoplasms; adrenal neoplasm; neoplasms, multiple primary; paraganglioma; pheochromocytoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal gland neoplasms; adrenal neoplasm; neoplasms, multiple primary; paraganglioma; pheochromocytoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenocarcinoma; carcinoma; hematologic neoplasms; hemochromatosis; myeloproliferative disorders; neoplasms; neoplasms, multiple primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; carcinoma; hematologic neoplasms; hemochromatosis; myeloproliferative disorders; neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple epiphyseal dysplasia; pseudoachondroplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple epiphyseal dysplasia; pseudoachondroplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis(ppmultiple sclerosis) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis(ppmultiple sclerosis) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

head and neck neoplasms; neoplasms, multiple primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease head and neck neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

head and neck neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; von hippel-lindau disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease head and neck neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; cholangitis, sclerosing; churg-strauss syndrome; colitis, ulcerative; crohn disease; lupus erythematosus, systemic; multiple sclerosis; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; amyotrophic lateral sclerosis; multiple system atrophy; nervous system diseases; parkinson disease; polyradiculoneuropathy, chronic inflammatory demyelinating; tauopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple endocrine neoplasia type 1; pituitary acth hypersecretion; pituitary neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple endocrine neoplasia type 1; pituitary acth hypersecretion; pituitary neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple myeloma; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple myeloma; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple familial trichoepithelioma and familial cylindromatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple familial trichoepithelioma and familial cylindromatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; systemic inflam response synd; systemic inflammatory response syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal gland neoplasms; adrenal neoplasm; carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; pheochromocytoma; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal gland neoplasms; adrenal neoplasm; carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; pheochromocytoma; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease; progressive supranuclear palsy; dementia, frontotemporal; multiple system atropy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoma; multiple myeloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoma; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

encephalomyelitis, autoimmune, experimental; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease encephalomyelitis, autoimmune, experimental; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; sepsis; systemic infection; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple system atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple autoimmune diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple autoimmune diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple endocrine neoplasia type 1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple endocrine neoplasia type 1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

laryngeal neoplasm; laryngeal neoplasms; neoplasms, multiple primary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease laryngeal neoplasm; laryngeal neoplasms; neoplasms, multiple primary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis, rheumatoid; atrial fibrillation; crohn disease; crohn's disease; diabetes mellitus type ii; diabetes mellitus, type 2; multiple sclerosis; rheumatoid arthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; congenital abnormalities; craniofacial abnormalities; syndrome; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; congenital abnormalities; craniofacial abnormalities; syndrome; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; postoperative complications; sepsis; septic shock; shock, septic; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; postoperative complications; sepsis; septic shock; shock, septic; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, medullary; multiple endocrine neoplasia type 2a; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, medullary; multiple endocrine neoplasia type 2a; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis; neuromyelitis optica Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis; neuromyelitis optica in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis, relapsing-remitting; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis, relapsing-remitting; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; multiple myeloma; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; multiple myeloma; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple endocrine neoplasia type 1; pancreatic neoplasm; pancreatic neoplasms; parathyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple endocrine neoplasia type 1; pancreatic neoplasm; pancreatic neoplasms; parathyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple myeloma; plasmacytoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple myeloma; plasmacytoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal gland neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; pheochromocytoma; von hippel-lindau disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal gland neoplasms; multiple endocrine neoplasia type 2a; paraganglioma; pheochromocytoma; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

normalized brain volume, multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease normalized brain volume, multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lupus erythematosus, systemic; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lupus erythematosus, systemic; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple chemical sensitivity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple chemical sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia; multiple myeloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pseudoachondroplasia and multiple epiphyseal dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pseudoachondroplasia and multiple epiphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, medullary; medullary carcinoma; multiple endocrine neoplasia type 2a; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melanoma; neoplasms, multiple primary; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melanoma; neoplasms, multiple primary; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; pneumonia; septic shock; shock, septic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; pneumonia; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple endocrine neoplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple endocrine neoplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; short bowel syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; short bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenoma; adrenal gland neoplasms; hyperparathyroidism; multiple endocrine neoplasia type 1; neuroendocrine tumors; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenoma; adrenal gland neoplasms; hyperparathyroidism; multiple endocrine neoplasia type 1; neuroendocrine tumors; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis; iga nephropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis; iga nephropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

churg-strauss syndrome; multiple sclerosis; wegener granulomatosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease churg-strauss syndrome; multiple sclerosis; wegener granulomatosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperinsulinism; hypoglycemia; insulinoma; multiple endocrine neoplasia type 1; pancreatic neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperinsulinism; hypoglycemia; insulinoma; multiple endocrine neoplasia type 1; pancreatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer's disease; parkinson's disease; multiple system atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer's disease; parkinson's disease; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

tic; combined vocal and multiple motor; tourette syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease tic; combined vocal and multiple motor; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

juvenile multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease juvenile multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell; multiple myeloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia, lymphocytic, chronic; leukemia, lymphocytic, chronic, b-cell; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple endocrine neoplasia type 2b Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple endocrine neoplasia type 2b in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple endocrine neoplasia type 2a Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple endocrine neoplasia type 2a in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leiomyoma; neoplasms, multiple primary; uterine neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leiomyoma; neoplasms, multiple primary; uterine neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis, chronic progressive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis, chronic progressive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 1; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 1; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infection; multiple myeloma; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infection; multiple myeloma; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myeloma, multiple Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myeloma, multiple in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hepatitis c, chronic; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hepatitis c, chronic; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; multiple sclerosis, relapsing-remitting Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis (severity) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis (severity) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, squamous cell; head and neck neoplasms; neoplasms, multiple primary; respiratory tract neoplasms; squamous cell carcinoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; head and neck neoplasms; neoplasms, multiple primary; respiratory tract neoplasms; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple oesophageal dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple oesophageal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, medullary; lymphatic metastasis; multiple endocrine neoplasia type 2a; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, medullary; lymphatic metastasis; multiple endocrine neoplasia type 2a; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

epstein-barr virus infections; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epstein-barr virus infections; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; mammary neoplasms; neoplasms, multiple primary; ovarian neoplasm; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; mammary neoplasms; neoplasms, multiple primary; ovarian neoplasm; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hereditary multiple exostoses Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hereditary multiple exostoses in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; neoplasms, multiple primary; ovarian neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; neoplasms, multiple primary; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

celiac disease; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease celiac disease; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple myeloma; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple myeloma; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple myeloma; pneumonia; sepsis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple myeloma; pneumonia; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; chromosome breakage; facies; growth disorders; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; chromosome breakage; facies; growth disorders; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis, relapsing-remitting Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis, relapsing-remitting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infection; multiple myeloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infection; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple organ failure; sepsis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; sepsis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone diseases; multiple myeloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone diseases; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoproliferative disorders; multiple myeloma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoproliferative disorders; multiple myeloma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenoma; colonic neoplasms; colonic polyps; neoplasms, multiple primary; precancerous conditions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenoma; colonic neoplasms; colonic polyps; neoplasms, multiple primary; precancerous conditions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

malaria, falciparum; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease malaria, falciparum; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple endocrine neoplasia type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple endocrine neoplasia type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; chromosome aberrations; chromosome abnormality; cystic fibrosis; echogenic bowel; fetal diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early onset of multiple sclerosis. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early onset of multiple sclerosis. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; craniofacial abnormalities; mouth abnormalities; pallister-hall syndrome; polydactyly; syndactyly Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; craniofacial abnormalities; mouth abnormalities; pallister-hall syndrome; polydactyly; syndactyly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia; multiple myeloma; myelodysplastic syndromes; preleukemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia; multiple myeloma; myelodysplastic syndromes; preleukemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

graft vs host disease; leukemia; multiple myeloma; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease graft vs host disease; leukemia; multiple myeloma; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple myeloma; neoplasm recurrence, local Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple myeloma; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dystonic disorders; multiple system atrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dystonic disorders; multiple system atrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple system atophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple system atophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple sclerosis, relapsing-remitting; myelitis; optic neuritis; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple sclerosis, relapsing-remitting; myelitis; optic neuritis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast neoplasms; carcinoma; multiple sclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; carcinoma; multiple sclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term multiple in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

MS (Multiple Sclerosis)_CNS - Spinal Cord (MMHCC)_GSE842 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during MS (Multiple Sclerosis)_CNS - Spinal Cord (MMHCC)_GSE842 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

MS (Multiple Sclerosis)_B Cell Lymphocyte_GSE10064 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during MS (Multiple Sclerosis)_B Cell Lymphocyte_GSE10064 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Multiple benign melanocytic nevi_Epidermis_GSE3189 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Multiple benign melanocytic nevi_Epidermis_GSE3189 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Multiple sclerosis--Brain Glutamate Levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple sclerosis--Brain Glutamate Levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Multiple myeloma Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple myeloma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Multiple sclerosis or amyotrophic lateral sclerosis Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple sclerosis or amyotrophic lateral sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Multiple sclerosis Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple sclerosis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Multiple myeloma (IgH translocation) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple myeloma (IgH translocation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Multiple sclerosis (severity) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple sclerosis (severity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Multiple myeloma (hyperdiploidy) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple myeloma (hyperdiploidy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Multiple sclerosis (OCB status) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple sclerosis (OCB status) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple cancers (lung cancer, gastric cancer, and squamous cell carcinoma) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Multiple sclerosis (age of onset) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Multiple sclerosis (age of onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

multiple myeloma Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease multiple myeloma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

multiple sclerosis Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease multiple sclerosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

multiple mitochondrial dna deletions Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the multiple mitochondrial dna deletions phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

multiple myeloma Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the multiple myeloma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

multiple exostoses Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple exostoses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple epiphyseal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple epiphyseal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple gastric polyps Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple gastric polyps phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple cutaneous leiomyomas Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple cutaneous leiomyomas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple impacted teeth Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple impacted teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple enchondromatosis Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple enchondromatosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple joint contractures Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple joint contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple rows of eyelashes Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple rows of eyelashes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple myeloma Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple myeloma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple plantar creases Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple plantar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ventricular preexcitation with multiple accessory pathways Gene Set

From HPO Gene-Disease Associations

genes associated with the ventricular preexcitation with multiple accessory pathways phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple digital exostoses Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple digital exostoses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple glomerular cysts Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple glomerular cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple suture craniosynostosis Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple suture craniosynostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple lipomas Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple lipomas phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of multiple cell lineages in the bone marrow Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of multiple cell lineages in the bone marrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple carpal ossification centers Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple carpal ossification centers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple mitochondrial dna deletions Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple mitochondrial dna deletions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple pterygia Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple pterygia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple cafe-au-lait spots Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple cafe-au-lait spots phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple palmar creases Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple palmar creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple lentigines Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple lentigines phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple renal cysts Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple renal cysts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple skeletal anomalies Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple skeletal anomalies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Multiple Trauma Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Trauma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple Organ Failure Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Organ Failure phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple Sclerosis, Chronic Progressive Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Sclerosis, Chronic Progressive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple Endocrine Neoplasia Type 2b Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Endocrine Neoplasia Type 2b phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple Endocrine Neoplasia Type 2a Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Endocrine Neoplasia Type 2a phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple Myeloma Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Myeloma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple Sclerosis, Relapsing-Remitting Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Sclerosis, Relapsing-Remitting phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Exostoses, Multiple Hereditary Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Exostoses, Multiple Hereditary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Abnormalities, Multiple Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Abnormalities, Multiple phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Hamartoma Syndrome, Multiple Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hamartoma Syndrome, Multiple phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple Endocrine Neoplasia Type 1 Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Endocrine Neoplasia Type 1 phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Acyl Coenzyme A Dehydrogenase Deficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple Endocrine Neoplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Endocrine Neoplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple System Atrophy Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple System Atrophy phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple Sclerosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Sclerosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Multiple Chemical Sensitivity Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Multiple Chemical Sensitivity phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Neoplasms, Multiple Primary Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Neoplasms, Multiple Primary phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

multiple major aortopulmonary collateral arteries Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the multiple major aortopulmonary collateral arteries phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

intestinal atresia, multiple Gene Set

From OMIM Gene-Disease Associations

genes associated with the intestinal atresia, multiple phenotype from the curated OMIM Gene-Disease Associations dataset.

?epiphyseal dysplasia, multiple, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?epiphyseal dysplasia, multiple, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 5, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 5, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

adenomas, multiple colorectal Gene Set

From OMIM Gene-Disease Associations

genes associated with the adenomas, multiple colorectal phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 9, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 9, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple endocrine neoplasia iib Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple endocrine neoplasia iib phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple endocrine neoplasia iia Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple endocrine neoplasia iia phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple pterygium syndrome, lethal type Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple pterygium syndrome, lethal type phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 3, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 3, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple myeloma, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple myeloma, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 1, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 1, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple sclerosis, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple sclerosis, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple system atrophy, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple system atrophy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple sclerosis, susceptibility to, 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple sclerosis, susceptibility to, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

orolaryngeal cancer, multiple, Gene Set

From OMIM Gene-Disease Associations

genes associated with the orolaryngeal cancer, multiple, phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple fibroadenomas of the breast Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple fibroadenomas of the breast phenotype from the curated OMIM Gene-Disease Associations dataset.

{vitiligo-associated multiple autoimmune disease susceptiblity 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {vitiligo-associated multiple autoimmune disease susceptiblity 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, with myopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, with myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 20, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 20, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

macrocephaly with multiple epiphyseal dysplasia and distinctive facies Gene Set

From OMIM Gene-Disease Associations

genes associated with the macrocephaly with multiple epiphyseal dysplasia and distinctive facies phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple mitochondrial dysfunctions syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple mitochondrial dysfunctions syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple mitochondrial dysfunctions syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple mitochondrial dysfunctions syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, multiple types, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, multiple types, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects, multiple types, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital heart defects, multiple types, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 14, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 14, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

venous malformations, multiple cutaneous and mucosal Gene Set

From OMIM Gene-Disease Associations

genes associated with the venous malformations, multiple cutaneous and mucosal phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 12, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 12, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 39, multiple types, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 39, multiple types, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, with myopia and deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, with myopia and deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple sclerosis, disease progression, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple sclerosis, disease progression, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple endocrine neoplasia, type iv Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple endocrine neoplasia, type iv phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple endocrine neoplasia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple endocrine neoplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

{vitiligo-associated multiple autoimmune disease susceptibility 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {vitiligo-associated multiple autoimmune disease susceptibility 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 34, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 34, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 11, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 11, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 6, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 6, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 2, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 2, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple myeloma, resistance to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple myeloma, resistance to} phenotype from the curated OMIM Gene-Disease Associations dataset.

pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 16, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 16, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 15, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 15, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

?multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple sulfatase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple sulfatase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?multiple synostoses syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?multiple synostoses syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple synostoses syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple synostoses syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple synostoses syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple synostoses syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple sclerosis, susceptibility to, 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple sclerosis, susceptibility to, 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple sclerosis, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple sclerosis, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple sclerosis, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple sclerosis, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

exostoses, multiple, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the exostoses, multiple, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

exostoses, multiple, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the exostoses, multiple, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

exostoses, multiple, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the exostoses, multiple, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 17, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 17, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 4, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 4, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 31, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 31, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 10, multiple types Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 10, multiple types phenotype from the curated OMIM Gene-Disease Associations dataset.

?multiple mitochondrial dysfunctions syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?multiple mitochondrial dysfunctions syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

trichoepithelioma, multiple familial, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the trichoepithelioma, multiple familial, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

trichoepithelioma, multiple familial, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the trichoepithelioma, multiple familial, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

{multiple self-healing squamous epithelioma, susceptiblity to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {multiple self-healing squamous epithelioma, susceptiblity to} phenotype from the curated OMIM Gene-Disease Associations dataset.

Resolution of AP sites via the multiple-nucleotide patch replacement pathway Gene Set

From Reactome Pathways 2014

proteins participating in the Resolution of AP sites via the multiple-nucleotide patch replacement pathway pathway from the Reactome Pathways dataset.

Defective HLCS causes multiple carboxylase deficiency Gene Set

From Reactome Pathways 2014

proteins participating in the Defective HLCS causes multiple carboxylase deficiency pathway from the Reactome Pathways dataset.

multiple myeloma cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue multiple myeloma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

multiple myeloma cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue multiple myeloma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Multiple Chronic Conditions Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Chronic Conditions in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Sclerosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Myeloma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Myeloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Sclerosis, Relapsing-Remitting Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Sclerosis, Relapsing-Remitting in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lipomatosis, Multiple Symmetrical Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lipomatosis, Multiple Symmetrical in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Vitiligo-Associated Multiple Autoimmune Disease Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Vitiligo-Associated Multiple Autoimmune Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Lipomata Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Lipomata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Adenomatous Polyps Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Adenomatous Polyps in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Endocrine Neoplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Endocrine Neoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Hereditary Multiple Exostoses Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Hereditary Multiple Exostoses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Epiphyseal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Epiphyseal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Pterygium Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Pterygium Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple System Atrophy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple System Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Acyl Coenzyme A Dehydrogenase Deficiency Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Acyl Coenzyme A Dehydrogenase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Gastrointestinal Atresias (Disorder) Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Gastrointestinal Atresias (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Familial Multiple Trichoepitheliomata Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Familial Multiple Trichoepitheliomata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Sclerosis, Primary Progressive Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Sclerosis, Primary Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Adnp-Related Multiple Congenital Anomalies, Intellectual Disability, Autism Spectrum Disorder Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Adnp-Related Multiple Congenital Anomalies, Intellectual Disability, Autism Spectrum Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Polyps Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Polyps in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Meningiomas, Multiple Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Meningiomas, Multiple in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Myeloma Progression Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Myeloma Progression in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Lacunar Infarcts Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Lacunar Infarcts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Familial Atypical Multiple Mole-Melanoma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Familial Atypical Multiple Mole-Melanoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Renal Cysts Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Renal Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Sclerosis, Acute Fulminating Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Sclerosis, Acute Fulminating in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Sclerosis, Acute Relapsing Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Sclerosis, Acute Relapsing in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Progressive Multiple Sclerosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Progressive Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Sclerosis In Children Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Sclerosis In Children in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Opticospinal Multiple Sclerosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Opticospinal Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Sulfatase Deficiency Disease Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Sulfatase Deficiency Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Carboxylase Deficiency Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Carboxylase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Joint Dislocations Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Joint Dislocations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Benign Multiple Sclerosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Benign Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Sclerosis Relapse Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Sclerosis Relapse in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Mitochondrial Dysfunctions Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Mitochondrial Dysfunctions Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Lentigines Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Lentigines in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Nevi Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Nevi in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple System Atrophy, Cerebellar Variant Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple System Atrophy, Cerebellar Variant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Sclerosis, Secondary Progressive Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Sclerosis, Secondary Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Fibrofolliculomas Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Fibrofolliculomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Asymptomatic Multiple Myeloma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Asymptomatic Multiple Myeloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Sclerosis, Chronic Progressive Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Sclerosis, Chronic Progressive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Self-Healing Squamous Epithelioma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Self-Healing Squamous Epithelioma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Biliary Hamartomas Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Biliary Hamartomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Pterygium Syndrome, Lethal Type Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Pterygium Syndrome, Lethal Type in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Epiphyseal Dysplasia, Multiple, With Myopia And Conductive Deafness Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Epiphyseal Dysplasia, Multiple, With Myopia And Conductive Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Epiphyseal Dysplasia, Multiple, With Myopathy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Epiphyseal Dysplasia, Multiple, With Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Linear Skin Defects With Multiple Congenital Anomalies Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Linear Skin Defects With Multiple Congenital Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Familial Multiple Factor Deficiency Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Familial Multiple Factor Deficiency Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Abscesses Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Abscesses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Familial Multiple Lipomatosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Familial Multiple Lipomatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Trichoepitheliomas Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Trichoepitheliomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Synostoses Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Synostoses Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Allergies Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Allergies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Severe Dermatitis, Multiple Allergies, Metabolic Wasting Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Severe Dermatitis, Multiple Allergies, Metabolic Wasting Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Malignant Neoplasm Of Lung - Multiple Primary Sites Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Malignant Neoplasm Of Lung - Multiple Primary Sites in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Basal Cell Papillomata Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Basal Cell Papillomata in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Exostoses, Multiple, Type Ii Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Exostoses, Multiple, Type Ii in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Hereditary Multiple Osteochondromas Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Hereditary Multiple Osteochondromas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Osteochondroma Of Long Bone Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Osteochondroma Of Long Bone in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Evanescent White Dot Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Evanescent White Dot Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Familial Multiple Trichodiscomas Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Familial Multiple Trichodiscomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Lung Cysts Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Lung Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Abnormality Of Multiple Cell Lineages In The Bone Marrow Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Abnormality Of Multiple Cell Lineages In The Bone Marrow in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Nevi Flammei, Familial Multiple Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Nevi Flammei, Familial Multiple in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Non-Ossifying Fibromatosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Non-Ossifying Fibromatosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Hemangioblastomas Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Hemangioblastomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Cysts Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Milia, Multiple Eruptive Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Milia, Multiple Eruptive in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Disability Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Disability in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Familial Multiple Coagulation Factor Deficiency Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Familial Multiple Coagulation Factor Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Pancreatic Beta-Cell Adenomas Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Pancreatic Beta-Cell Adenomas in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Exacerbation Of Multiple Sclerosis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Exacerbation Of Multiple Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Indolent Multiple Myeloma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Indolent Multiple Myeloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Pterygium Syndrome, Autosomal Dominant Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Pterygium Syndrome, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Cranial Neuropathies, Multiple Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Cranial Neuropathies, Multiple in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Fibroadenomas Of The Breast Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Fibroadenomas Of The Breast in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Digital Exostoses Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Digital Exostoses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Lentigines/Leopard Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Lentigines/Leopard Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Lineage Myelodysplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Lineage Myelodysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Cranial Nerve Palsy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Cranial Nerve Palsy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Aneurysms Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Aneurysms in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple, Subcutaneous Nodules Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple, Subcutaneous Nodules in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Venous Malformations, Multiple Cutaneous And Mucosal Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Venous Malformations, Multiple Cutaneous And Mucosal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Sclerosis Lesion Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Sclerosis Lesion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Self-Healing Epithelioma Of Ferguson-Smith Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Self-Healing Epithelioma Of Ferguson-Smith in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Familial Multiple Myeloma Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Familial Multiple Myeloma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Ventricular Septal Defects Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Multiple Ventricular Septal Defects in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Multiple Tumors Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Tumors in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Malignancy Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Malignancy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Organ Failure Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Organ Failure in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Unerupted Teeth Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Unerupted Teeth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple System Atrophy Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple System Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Suture Craniosynostosis Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Suture Craniosynostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Skeletal Anomalies Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Skeletal Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Glomerular Cysts Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Glomerular Cysts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Palmar Creases Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Palmar Creases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Plantar Creases Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Plantar Creases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Joint Dislocations Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Joint Dislocations in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Chemical Sensitivity Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Chemical Sensitivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Myeloma, T(11;14) Type, Susceptibility To Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Myeloma, T(11;14) Type, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Impacted Teeth Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Impacted Teeth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Cancer Of Multiple Types, Susceptibility To Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Cancer Of Multiple Types, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Pterygia Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Pterygia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Contractures Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Contractures in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Carpal Ossification Centers Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Carpal Ossification Centers in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Long-Bone Exostoses Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Long-Bone Exostoses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Facial Dysmorphism With Multiple Malformations Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Facial Dysmorphism With Multiple Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Neoplasms, Multiple Primary Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Neoplasms, Multiple Primary in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Anti-Multiple Nuclear Dots Antibody Positivity Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Anti-Multiple Nuclear Dots Antibody Positivity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Mitochondrial Dna Deletions Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Mitochondrial Dna Deletions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Ventricular Preexcitation With Multiple Accessory Pathways Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Ventricular Preexcitation With Multiple Accessory Pathways in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Self-Healing Squamous Epithelioma, Susceptibility To Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Self-Healing Squamous Epithelioma, Susceptibility To in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Multiple Rows Of Eyelashes Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Multiple Rows Of Eyelashes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

multiple spine synapse organization, single dendrite Gene Set

From GO Biological Process Annotations 2023

genes participating in the multiple spine synapse organization, single dendrite biological process from the curated GO Biological Process Annotations 2023 dataset.

multiple spine synapse organization Gene Set

From GO Biological Process Annotations 2023

genes participating in the multiple spine synapse organization biological process from the curated GO Biological Process Annotations 2023 dataset.

CUX1-19635798-MULTIPLE-CANCER-TYPES-HUMAN Gene Set

From ChEA Transcription Factor Targets 2022

target genes of the CUX1-19635798-MULTIPLE-CANCER-TYPES-HUMAN transcription factor in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.

multiple major aortopulmonary collateral arteries Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the multiple major aortopulmonary collateral arteries phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

multiple persisting craniopharyngeal ducts Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the multiple persisting craniopharyngeal ducts phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Multiple pluripotent progenitor cell_Bone marrow_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Multiple pluripotent progenitor cell_Bone marrow_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Multiple myeloma(MM) cell_Bone marrow_Human Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Multiple myeloma(MM) cell_Bone marrow_Human cell type from the CellMarker Gene-Cell Type Associations dataset.

Multiple ductal cell_Pancreatic duct_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Multiple ductal cell_Pancreatic duct_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Multiple epiphyseal dysplasia and pseudoachondroplasia genes Gene Set

From WikiPathways Pathways 2024

proteins participating in the Multiple epiphyseal dysplasia and pseudoachondroplasia genes pathway from the WikiPathways Pathways 2024 dataset.

Defective HLCS causes multiple carboxylase deficiency Gene Set

From Reactome Pathways 2024

proteins participating in the Defective HLCS causes multiple carboxylase deficiency pathway from the Reactome Pathways 2024 dataset.

Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models Gene Set

From Reactome Pathways 2024

proteins participating in the Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models pathway from the Reactome Pathways 2024 dataset.

Resolution of AP sites via the multiple-nucleotide patch replacement pathway Gene Set

From Reactome Pathways 2024

proteins participating in the Resolution of AP sites via the multiple-nucleotide patch replacement pathway pathway from the Reactome Pathways 2024 dataset.

multiple spine synapse organization, single dendrite Gene Set

From GO Biological Process Annotations 2025

genes participating in the multiple spine synapse organization, single dendrite biological process from the curated GO Biological Process Annotations 2025 dataset.

multiple spine synapse organization Gene Set

From GO Biological Process Annotations 2025

genes participating in the multiple spine synapse organization biological process from the curated GO Biological Process Annotations 2025 dataset.

Multiple endocrine neoplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Multiple endocrine neoplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Multiple endocrine neoplasia type 2A Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Multiple endocrine neoplasia type 2A from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Hereditary multiple exostoses Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Hereditary multiple exostoses from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Multiple myeloma Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Multiple myeloma from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Noonan syndrome with multiple lentigines Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Noonan syndrome with multiple lentigines from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Multiple mitochondrial dysfunctions syndrome Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Multiple mitochondrial dysfunctions syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Multiple carboxylase deficiency Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Multiple carboxylase deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Multiple epiphyseal dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Multiple epiphyseal dysplasia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Multiple sclerosis Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Multiple sclerosis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Multiple system atrophy Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Multiple system atrophy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Multiple acyl-CoA dehydrogenase deficiency Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Multiple acyl-CoA dehydrogenase deficiency from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Multiple cutaneous and mucosal venous malformations Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Multiple cutaneous and mucosal venous malformations from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Linear skin defects with multiple congenital anomalies 1 Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Linear skin defects with multiple congenital anomalies 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Multiple myeloma Gene Set

From DISEASES Experimental Gene-Disease Association Evidence Scores 2025

genes associated with the disease Multiple myeloma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple myeloma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple myeloma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple sclerosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple synostoses syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple synostoses syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple acyl-CoA dehydrogenase deficiency Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple acyl-CoA dehydrogenase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple mitochondrial dysfunctions syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Hereditary multiple exostoses Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Hereditary multiple exostoses in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Primary progressive multiple sclerosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Primary progressive multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Secondary progressive multiple sclerosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Secondary progressive multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

relapsing-remitting multiple sclerosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease relapsing-remitting multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple endocrine neoplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple endocrine neoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple endocrine neoplasia type 2B Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple endocrine neoplasia type 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple personality disorder Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple personality disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple intestinal atresia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple intestinal atresia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple carboxylase deficiency Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple carboxylase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Hereditary arterial and articular multiple calcification syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Hereditary arterial and articular multiple calcification syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple endocrine neoplasia type 2A Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple endocrine neoplasia type 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple synostoses syndrome 1 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple synostoses syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Cataract 9 multiple types Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Cataract 9 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple epiphyseal dysplasia 1 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple epiphyseal dysplasia 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Noonan syndrome with multiple lentigines Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Noonan syndrome with multiple lentigines in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple synostoses syndrome 3 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple synostoses syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple system atrophy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple system atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Familial multiple lipomatosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Familial multiple lipomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple symmetric lipomatosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple symmetric lipomatosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple chemical sensitivity Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple chemical sensitivity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple endocrine neoplasia type 1 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple endocrine neoplasia type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Progressive relapsing multiple sclerosis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Progressive relapsing multiple sclerosis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple cranial nerve palsy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple cranial nerve palsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome 4 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple congenital anomalies-hypotonia-seizures syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple epiphyseal dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple epiphyseal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Cataract 8 multiple types Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Cataract 8 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple epiphyseal dysplasia 5 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple epiphyseal dysplasia 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Linear skin defects with multiple congenital anomalies 1 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Linear skin defects with multiple congenital anomalies 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Cataract 6 multiple types Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Cataract 6 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple synostoses syndrome 2 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple synostoses syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Familial multiple nevi flammei Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Familial multiple nevi flammei in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple endocrine neoplasia type 4 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple endocrine neoplasia type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple cutaneous and mucosal venous malformations Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple cutaneous and mucosal venous malformations in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Cataract 1 multiple types Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Cataract 1 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Noonan syndrome with multiple lentigines 2 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Noonan syndrome with multiple lentigines 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Cataract 32 multiple types Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Cataract 32 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Noonan syndrome with multiple lentigines 1 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Noonan syndrome with multiple lentigines 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple mitochondrial dysfunctions syndrome 3 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple mitochondrial dysfunctions syndrome 2 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple benign circumferential skin creases on limbs Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple benign circumferential skin creases on limbs in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple epiphyseal dysplasia 3 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple epiphyseal dysplasia 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple epiphyseal dysplasia due to collagen 9 anomaly Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple epiphyseal dysplasia due to collagen 9 anomaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple mitochondrial dysfunctions syndrome 1 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Cataract 4 multiple types Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Cataract 4 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Cataract 11 multiple types Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Cataract 11 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Cataract 10 multiple types Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Cataract 10 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple mitochondrial dysfunctions syndrome 4 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Cataract 3 multiple types Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Cataract 3 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Cataract 21 multiple types Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Cataract 21 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple mucosal neuroma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple mucosal neuroma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Cataract 31 multiple types Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Cataract 31 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple epiphyseal dysplasia 4 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple epiphyseal dysplasia 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Cataract 14 multiple types Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Cataract 14 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple epiphyseal dysplasia 7 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple epiphyseal dysplasia 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple mitochondrial dysfunctions syndrome 6 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Cataract 34 multiple types Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Cataract 34 multiple types in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Linear skin defects with multiple congenital anomalies 3 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Linear skin defects with multiple congenital anomalies 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Linear skin defects with multiple congenital anomalies 2 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Linear skin defects with multiple congenital anomalies 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Noonan syndrome with multiple lentigines 3 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Noonan syndrome with multiple lentigines 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple epiphyseal dysplasia with myopia and deafness Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple epiphyseal dysplasia with myopia and deafness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple mitochondrial dysfunctions syndrome 5 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple mitochondrial dysfunctions syndrome 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple epiphyseal dysplasia 2 Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Multiple epiphyseal dysplasia 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Multiple myeloma cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Multiple myeloma cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Multiple myeloma cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Multiple myeloma cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Multiple synapse bouton Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Multiple synapse bouton cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Multiple synapse bouton, contacting single dendrite Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Multiple synapse bouton, contacting single dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Familial multiple polyposis syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Familial multiple polyposis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Multiple system atrophy Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Multiple system atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Multiple symmetric lipomatosis Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Multiple symmetric lipomatosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Multiple congenital exostosis Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Multiple congenital exostosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Multiple acyl-CoA dehydrogenase deficiency Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Multiple acyl-CoA dehydrogenase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Multiple sulfatase deficiency Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Multiple sulfatase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Multiple epiphyseal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Multiple epiphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Vitiligo-associated multiple autoimmune disease susceptibility Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Vitiligo-associated multiple autoimmune disease susceptibility phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Familial multiple trichoepitheliomata Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Familial multiple trichoepitheliomata phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Cataract 12 multiple Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Cataract 12 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Multiple myeloma Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Multiple myeloma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Multiple synostoses syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Multiple synostoses syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Cataract 1 multiple Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Cataract 1 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Multiple cutaneous and mucosal venous malformations Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Multiple cutaneous and mucosal venous malformations phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Multiple sclerosis Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Multiple sclerosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Multiple self-healing squamous epithelioma Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Multiple self-healing squamous epithelioma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

MULTIPLE MYEL Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the MULTIPLE MYEL phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Multiple endocrine neoplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Multiple endocrine neoplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

MULTIPLE ENDOCRINE NEOPLA Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the MULTIPLE ENDOCRINE NEOPLA phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Cataract 4 multiple Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Cataract 4 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Cataract 3 multiple Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Cataract 3 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Cataract 9 multiple Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Cataract 9 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Autosomal recessive multiple pterygium syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Autosomal recessive multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lethal multiple pterygium syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lethal multiple pterygium syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Hereditary arterial and articular multiple calcification syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Hereditary arterial and articular multiple calcification syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

MULTIPLE JOINT DISLOCATI Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the MULTIPLE JOINT DISLOCATI phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Multiple joint dislocations Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Multiple joint dislocations phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Multiple mitochondrial dysfunctions syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Multiple mitochondrial dysfunctions syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Cataract 16 multiple Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Cataract 16 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Cataract 39 multiple Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Cataract 39 multiple phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Multiple renal cysts Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Multiple renal cysts phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.