| Name |
|---|
CMAP Signatures of Differentially Expressed Genes for Small Molecules DatasetFrom Connectivity Map mRNA expression profiles for cell lines following chemical perturbation |
GEO Signatures of Differentially Expressed Genes for Small Molecules DatasetmRNA 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 |
HMN7A GeneMotor neuronopathy, distal hereditary, type VIIA |
DLX5 Genedistal-less homeobox 5 This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein may play a role in bone development and fracture healing. Mutation in this gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation. [provided by RefSeq, Jul 2008] |
DLX6 Genedistal-less homeobox 6 This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. This family is comprised of at least 6 different members that encode proteins with roles in forebrain and craniofacial development. This gene is in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7. [provided by RefSeq, Jul 2008] |
DLX1 Genedistal-less homeobox 1 This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein is localized to the nucleus where it may function as a transcriptional regulator of signals from multiple TGF-{beta} superfamily members. The encoded protein may play a role in the control of craniofacial patterning and the differentiation and survival of inhibitory neurons in the forebrain. This gene is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 2. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008] |
DLX2 Genedistal-less homeobox 2 Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. The DLX proteins are postulated to play a role in forebrain and craniofacial development. This gene is located in a tail-to-tail configuration with another member of the gene family on the long arm of chromosome 2. [provided by RefSeq, Jul 2008] |
DLX3 Genedistal-less homeobox 3 Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. Trichodentoosseous syndrome (TDO), an autosomal dominant condition, has been correlated with DLX3 gene mutation. This gene is located in a tail-to-tail configuration with another member of the gene family on the long arm of chromosome 17. Mutations in this gene have been associated with the autosomal dominant conditions trichodentoosseous syndrome and amelogenesis imperfecta with taurodontism. [provided by RefSeq, Jul 2008] |
DEL22Q11.2 GeneChromosome 22q11.2 deletion syndrome, distal |
DLX4 Genedistal-less homeobox 4 Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. The DLX proteins are postulated to play a role in forebrain and craniofacial development. Three transcript variants have been described for this gene, however, the full length nature of one variant has not been described. Studies of the two splice variants revealed that one encoded isoform functions as a repressor of the beta-globin gene while the other isoform lacks that function. [provided by RefSeq, Jul 2008] |
WDM GeneWelander distal myopathy |
SYM2 Genesymphalangism 2 (distal) |
SMAR GeneSpinal muscular atrophy, chronic distal, autosomal recessive |
HMNJ GeneDistal hereditary motor neuropathy, Jerash type |
DA4 Genearthrogryposis, distal, type 4 |
DEL7Q11.23 GeneChromosome 7q11.23 deletion syndrome, distal, 1.2Mb |
MPD3 GeneMyopathy, distal 3 |
HOTTIP GeneHOXA distal transcript antisense RNA This gene produces a long RNA in antisense to the HOXA gene cluster. This transcript may regulate expression of HOXA genes in cis. This gene is upregulated in tumors and is implicated in the promotion of cell proliferation. [provided by RefSeq, Dec 2017] |
DMAC2L Genedistal membrane arm assembly component 2 like This gene encodes a subunit of mitochondrial ATP synthase. Mitochondrial ATP synthase catalyzes ATP synthesis, utilizing an electrochemical gradient of protons across the inner membrane during oxidative phosphorylation. ATP synthase is composed of two linked multi-subunit complexes: the soluble catalytic core, F1, and the membrane-spanning component, Fo, comprising the proton channel. This gene encodes the subunit s, also known as factor B, of the proton channel. This subunit is necessary for the energy transduction activity of the ATP synthase complexes. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008] |
DMAC2 Genedistal membrane arm assembly component 2 Involved in mitochondrial respiratory chain complex I assembly. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
DMAC1 Genedistal membrane arm assembly component 1 Involved in mitochondrial respiratory chain complex I assembly. Located in mitochondrial inner membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNU5B-1 GeneRNA, 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 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 6 |
LOC101928952 Geneserine palmitoyltransferase small subunit A pseudogene |
RNU6-67P GeneRNA, U6 small nuclear 67, pseudogene |
RNU7-36P GeneRNA, U7 small nuclear 36 pseudogene |
SNORA81 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U1 small nuclear 16, pseudogene |
KRR1 GeneKRR1, 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 GeneRNA, U7 small nuclear 53 pseudogene |
RNU5A-5P GeneRNA, U5A small nuclear 5, pseudogene |
SNORD48 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Generas-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2) pseudogene |
LOC100422227 Genesmall ubiquitin-like modifier 1 pseudogene |
U2AF1L4 GeneU2 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 GeneRNA, U2 small nuclear 6, pseudogene |
SNORD91B Genesmall 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 Genesmall 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 Genesmall nuclear ribonucleoprotein 27kDa (U4/U6.U5) pseudogene |
SNORD115-6 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneLSM5 homolog, U6 small nuclear RNA associated (S. cerevisiae) pseudogene |
LOC100820733 GeneLSM2 homolog, U6 small nuclear RNA associated (S. cerevisiae) pseudogene |
RNU7-1 GeneRNA, U7 small nuclear 1 Implicated in Aicardi-Goutieres syndrome. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-46P GeneRNA, U6 small nuclear 46, pseudogene |
SERF2 Genesmall 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 Genesmall 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 Genecarboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene |
SNORD111B Genesmall 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 GeneM-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene |
LOC100631267 GeneM-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene |
LOC100631266 GeneM-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene |
LOC100631268 GeneM-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene |
RNU5E-6P GeneRNA, U5E small nuclear 6, pseudogene |
RNU7-24P GeneRNA, U7 small nuclear 24 pseudogene |
SNRPD3 Genesmall 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 Genesmall 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 Genesmall 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 GeneM-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 Genesmall EDRK-rich factor 2 pseudogene |
RNU1-28P GeneRNA, U1 small nuclear 28, pseudogene |
RNU1-13P GeneRNA, U1 small nuclear 13, pseudogene |
RNU7-5P GeneRNA, U7 small nuclear 5 pseudogene |
SPRR4 Genesmall 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 Genesmall 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 GeneRNA, U6atac small nuclear 5, pseudogene |
LSM8 GeneLSM8 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 GeneLSM4 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 GeneLSM5 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 GeneLSM6 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 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 9 |
SNRPGP7 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 7 |
SNRPGP6 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 6 |
SNRPGP5 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 5 |
SNRPGP4 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 4 |
SNRPGP1 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 1 |
LOC100129534 Genesmall nuclear ribonucleoprotein polypeptide N pseudogene |
LOC101927923 Genesmall integral membrane protein 12-like |
LOC100131747 Genesmall EDRK-rich factor 2 pseudogene |
SNORD12C Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 62 pseudogene |
RNU6-79P GeneRNA, U6 small nuclear 79, pseudogene |
RNU4-7P GeneRNA, U4 small nuclear 7, pseudogene |
RNU6-8 GeneRNA, 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 GeneRNA, 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 GeneRNA, 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 GeneRNA, 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 GeneRNA, 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 GeneRNA, U6 small nuclear 69, pseudogene |
SNORA9 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U1 small nuclear 20, pseudogene |
LOC100421121 Genesmall G protein signaling modulator 1 pseudogene |
RRP9 Generibosomal 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 Genesmall integral membrane protein 13 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM12 Genesmall integral membrane protein 12 Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM11 Genesmall integral membrane protein 11 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM10 Genesmall integral membrane protein 10 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM17 Genesmall integral membrane protein 17 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM15 Genesmall integral membrane protein 15 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM14 Genesmall 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 Genesmall integral membrane protein 19 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM18 Genesmall integral membrane protein 18 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-47P GeneRNA, U7 small nuclear 47 pseudogene |
RNU7-86P GeneRNA, U7 small nuclear 86 pseudogene |
SNORD121B Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 13 pseudogene |
RNU6-36P GeneRNA, U6 small nuclear 36, pseudogene |
RNU4ATAC2P GeneRNA, U4atac small nuclear 2, pseudogene |
RNU6-64P GeneRNA, U6 small nuclear 64, pseudogene |
SNRNP200 Genesmall 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 GeneRNA, U5B small nuclear 5, pseudogene |
RNU6-63P GeneRNA, U6 small nuclear 63, pseudogene |
SNORA74A Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 54 pseudogene |
RNU5A-2P GeneRNA, U5A small nuclear 2, pseudogene |
SNORD115-43 Genesmall 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 Genesmall 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 Genesmall nucleolar RNA, C/D box 115-47 |
SNORD1A Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 32 pseudogene |
SNORD43 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall ILF3/NF90-associated RNA F |
SNAR-E Genesmall ILF3/NF90-associated RNA E Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-D Genesmall ILF3/NF90-associated RNA D |
KCNN4 Genepotassium 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 Genepotassium 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 Genepotassium 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 Genepotassium 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 GeneRNA, U7 small nuclear 33 pseudogene |
RNU5D-2P GeneRNA, U5D small nuclear 2, pseudogene |
SNORA33 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U6 small nuclear 76, pseudogene |
RNU7-27P GeneRNA, U7 small nuclear 27 pseudogene |
SNRPCP9 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 9 |
SNRPCP8 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 8 |
SNRPCP3 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 3 |
SNRPCP2 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 2 |
SNRPCP7 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 7 |
SNRPCP4 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 4 |
SNAPC3 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U6 small nuclear 21, pseudogene |
UTP14A GeneUTP14, 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 GeneUTP14, 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 GeneRNA, U2 small nuclear 3, pseudogene |
RNU7-75P GeneRNA, U7 small nuclear 75 pseudogene |
RNU7-4P GeneRNA, U7 small nuclear 4 pseudogene |
RN7SKP1 GeneRNA, 7SK small nuclear pseudogene 1 |
LOC102724525 Genecarboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene |
RNU5A-8P GeneRNA, U5A small nuclear 8, pseudogene |
RNU6-53P GeneRNA, U6 small nuclear 53, pseudogene |
RNU6-39P GeneRNA, U6 small nuclear 39, pseudogene |
RNU5F-6P GeneRNA, U5F small nuclear 6, pseudogene |
SNAR-A8 Genesmall ILF3/NF90-associated RNA A8 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU4-4P GeneRNA, U4 small nuclear 4, pseudogene |
SNAR-G1 Genesmall ILF3/NF90-associated RNA G1 |
SNAR-G2 Genesmall ILF3/NF90-associated RNA G2 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-83P GeneRNA, U6 small nuclear 83, pseudogene |
RNU1-27P GeneRNA, U1 small nuclear 27, pseudogene |
RNU6-48P GeneRNA, U6 small nuclear 48, pseudogene |
RNU1-18P GeneRNA, U1 small nuclear 18, pseudogene |
SMIM23 Genesmall integral membrane protein 23 Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM20 Genesmall 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 Genesmall integral membrane protein 21 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM24 Genesmall integral membrane protein 24 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RNU2-1 GeneRNA, 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 GeneRNA, U7 small nuclear 42 pseudogene |
SNORD32A Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 85 pseudogene |
SCLC1 Genesmall cell cancer of the lung |
SNORD17 Genesmall 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 Genesmall 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 Genesmall nucleolar RNA host gene 4 |
SNHG7 Genesmall 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 Genesmall nucleolar RNA host gene 6 |
SNHG1 Genesmall 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 Genesmall nucleolar RNA host gene 8 |
RNU7-28P GeneRNA, U7 small nuclear 28 pseudogene |
RNU7-65P GeneRNA, U7 small nuclear 65 pseudogene |
RNU7-38P GeneRNA, U7 small nuclear 38 pseudogene |
SNORD15B Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall nuclear ribonucleoprotein polypeptide B pseudogene |
LOC100421672 Genesmall nuclear ribonucleoprotein polypeptide B pseudogene |
LOC101929749 Genecarboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene |
TSKU Genetsukushi, 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 Geneu3 small nucleolar ribonucleoprotein protein MPP10-like |
SNORD83A Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U6 small nuclear 66, pseudogene |
SNORD85 Genesmall 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 GeneUTP3, 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 GeneRNA, U7 small nuclear 8 pseudogene |
SNORD114-31 Genesmall 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 Genesmall 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 Genesmall lysine-rich protein 1 |
LOC100820734 GeneLSM2 homolog, U6 small nuclear RNA associated (S. cerevisiae) pseudogene |
RNU7-14P GeneRNA, U7 small nuclear 14 pseudogene |
LOC729200 Genesmall nuclear ribonucleoprotein polypeptide B pseudogene |
RNVU1-17 GeneRNA, 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 GeneRNA, 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 GeneRNA, 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 GeneRNA, 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 GeneRNA, 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 GeneRNA, 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 Genesmall 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 GeneRNA, U7 small nuclear 30 pseudogene |
SNORD13 Genesmall 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 Genesmall integral membrane protein 11 pseudogene 1 |
SNORA68 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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@ Genesmall nucleolar RNA, C/D box 116 cluster |
SNAPC5P1 Genesmall nuclear RNA activating complex, polypeptide 5, 19kDa pseudogene 1 |
SNRPGP13 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 13 |
SNRPGP12 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 12 |
SNRPGP11 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 11 |
SNRPGP14 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 14 |
SNORD116-25 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U5E small nuclear 8, pseudogene |
RNU7-51P GeneRNA, U7 small nuclear 51 pseudogene |
SNORD65 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U6 small nuclear 15, pseudogene |
RNU2-4P GeneRNA, U2 small nuclear 4, pseudogene |
RNU1-15P GeneRNA, U1 small nuclear 15, pseudogene |
RNU5F-4P GeneRNA, U5F small nuclear 4, pseudogene |
RNU6ATAC3P GeneRNA, U6atac small nuclear 3, pseudogene |
SVIP Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 72 pseudogene |
RNU6-56P GeneRNA, U6 small nuclear 56, pseudogene |
SNORD114-20 Genesmall 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 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 8 |
SNORD115-21 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2 pseudogene |
RNU3P2 GeneRNA, U3 small nucleolar pseudogene 2 |
RNU3P3 GeneRNA, 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 GeneRNA, U3 small nucleolar pseudogene 1 |
RNU3P4 GeneRNA, U3 small nucleolar pseudogene 4 |
SNHG15 Genesmall 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 Genesmall 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 Genesmall nucleolar RNA host gene 17 |
SNHG16 Genesmall nucleolar RNA host gene 16 |
SNHG11 Genesmall 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 Genesmall 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 Genesmall nucleolar RNA host gene 19 |
SNHG18 Genesmall nucleolar RNA host gene 18 |
SNORA80E Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U4 small nuclear 9, pseudogene |
RNU6-71P GeneRNA, U6 small nuclear 71, pseudogene |
SNORA45A Genesmall 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 GeneRNA, U7 small nuclear 22 pseudogene |
SNRPB2 Genesmall 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 Geneash2 (absent, small, or homeotic)-like (Drosophila) pseudogene 1 |
RNU7-59P GeneRNA, U7 small nuclear 59 pseudogene |
SNORD88A Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U6 small nuclear 26, pseudogene |
UTP11L GeneUTP11-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 GeneRNA, U6 small nuclear 10, pseudogene |
SNORD114-1 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Geneash1 (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 GeneUTP6, small subunit (SSU) processome component, homolog (yeast) pseudogene |
LOC100422497 GeneUTP18, small subunit (SSU) processome component, homolog (yeast) pseudogene |
RNU7-41P GeneRNA, U7 small nuclear 41 pseudogene |
SCARNA27 Genesmall Cajal body-specific RNA 27 |
SCARNA22 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U6atac small nuclear 4, pseudogene |
RNU1-3 GeneRNA, 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 GeneRNA, 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 GeneRNA, U6 small nuclear 31, pseudogene |
SNORD115-5 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 60 pseudogene |
LOC441722 GeneU2 small nuclear RNA auxiliary factor 1-like 4 pseudogene |
SNORD23 Genesmall 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 Genesmall ILF3/NF90-associated RNA B2 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-B1 Genesmall ILF3/NF90-associated RNA B1 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU5B-3P GeneRNA, U5B small nuclear 3, pseudogene |
LOC100631374 GeneM-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene |
SNRNP40 Genesmall 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 Genesmall 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 GeneCDC42 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 GeneCDC42 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 GeneRNA, U1 small nuclear 22, pseudogene |
SCARNA5 Genesmall 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 Genesmall 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 Genesmall cell adhesion glycoprotein Located in cell junction; nucleoplasm; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
RN7SKP8 GeneRNA, 7SK small nuclear pseudogene 8 |
RN7SKP9 GeneRNA, 7SK small nuclear pseudogene 9 |
RN7SKP6 GeneRNA, 7SK small nuclear pseudogene 6 |
RN7SKP7 GeneRNA, 7SK small nuclear pseudogene 7 |
RN7SKP4 GeneRNA, 7SK small nuclear pseudogene 4 |
RN7SKP5 GeneRNA, 7SK small nuclear pseudogene 5 |
RN7SKP2 GeneRNA, 7SK small nuclear pseudogene 2 |
RN7SKP3 GeneRNA, 7SK small nuclear pseudogene 3 |
SCARNA2 Genesmall 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 Genesmall nucleolar RNA host gene 3 Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM2 Genesmall integral membrane protein 2 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM1 Genesmall 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 Genesmall nucleolar RNA host gene 9 |
RNU7-80P GeneRNA, U7 small nuclear 80 pseudogene |
RNU7-11P GeneRNA, U7 small nuclear 11 pseudogene |
LOC643605 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase like 2 pseudogene |
RNU7-35P GeneRNA, U7 small nuclear 35 pseudogene |
SNORD45C Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 68 pseudogene |
SNORD18A Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall integral membrane protein 10 like 1 Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA76C Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 52 pseudogene |
RNU5A-4P GeneRNA, U5A small nuclear 4, pseudogene |
SNORD3D Genesmall 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@ Genesmall nucleolar RNA, C/D box 3 cluster |
SNORD3A Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U6 small nuclear 45, pseudogene |
RNU6-34P GeneRNA, U6 small nuclear 34, pseudogene |
LSM1P1 GeneLSM1, U6 small nuclear RNA associated pseudogene 1 |
LOC102724677 Genecarboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene |
RNU6-55P GeneRNA, U6 small nuclear 55, pseudogene |
SNORA19 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U5F small nuclear 7, pseudogene Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-19P GeneRNA, U7 small nuclear 19 pseudogene |
RNU7-78P GeneRNA, U7 small nuclear 78 pseudogene |
RNU4ATAC GeneRNA, 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 GeneRNA, U7 small nuclear 25 pseudogene |
RNU7-81P GeneRNA, U7 small nuclear 81 pseudogene |
SNAR-C3 Genesmall ILF3/NF90-associated RNA C3 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU6-23P GeneRNA, U6 small nuclear 23, pseudogene |
RNU7-10P GeneRNA, U7 small nuclear 10 pseudogene |
CTDSP1 GeneCTD (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 GeneCTD (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 GeneCTD (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 GeneRNA, U7 small nuclear 20 pseudogene |
SNORD116-10 Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 6 pseudogene |
RNU7-77P GeneRNA, U7 small nuclear 77 pseudogene |
RN7SK GeneRNA, 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 GeneUTP18 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 Genesmall 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 Genesmall ILF3/NF90-associated RNA A14 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-A11 Genesmall ILF3/NF90-associated RNA A11 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-A10 Genesmall ILF3/NF90-associated RNA A10 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD3C Genesmall 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 Genesmall 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 GeneRNA, 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 GeneRNA, U4 small nuclear 6, pseudogene |
SNORA71D Genesmall 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 GeneLSM3 homolog, U6 small nuclear RNA associated (S. cerevisiae) pseudogene |
SNAR-A3 Genesmall ILF3/NF90-associated RNA A3 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-A2 Genesmall ILF3/NF90-associated RNA A2 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-A7 Genesmall ILF3/NF90-associated RNA A7 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-A6 Genesmall ILF3/NF90-associated RNA A6 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-A5 Genesmall ILF3/NF90-associated RNA A5 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-A4 Genesmall ILF3/NF90-associated RNA A4 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA16A Genesmall 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 Genecms1 ribosomal small subunit homolog (yeast) Enables RNA binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
SNRNP70 Genesmall 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 GeneRNA, U7 small nuclear 49 pseudogene |
RNU5E-1 GeneRNA, 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 Genesmall 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 GeneRNA, U1 small nuclear 21, pseudogene |
LOC100421863 Geneash2 (absent, small, or homeotic)-like (Drosophila) pseudogene |
RNU7-44P GeneRNA, U7 small nuclear 44 pseudogene |
SNORD116-5 Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 87 pseudogene |
RNU7-12P GeneRNA, U7 small nuclear 12 pseudogene |
RNU6ATAC GeneRNA, 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 Genesmall 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 Genesmall integral membrane protein 12 pseudogene 1 |
SPTSSA Geneserine 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 Geneserine 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 Genesmall 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 Genesmall 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 Genesmall 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 Genecarboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2 pseudogene |
UTP6 GeneUTP6, 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 Genesmall 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 Genesmall 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 Genesmall EDRK-rich factor 2 pseudogene |
RSG1 GeneREM2 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 GeneRNA, U5B small nuclear 6, pseudogene |
SNORA73A Genesmall 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 Genesmall nucleolar RNA, H/ACA box 73B |
RNU7-57P GeneRNA, U7 small nuclear 57 pseudogene |
RNU6-52P GeneRNA, U6 small nuclear 52, pseudogene |
RAC2 Generas-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 Generas-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 Generas-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 Genesmall ILF3/NF90-associated RNA A12 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-88P GeneRNA, U7 small nuclear 88 pseudogene |
RN7SKP10 GeneRNA, 7SK small nuclear pseudogene 10 |
BA395L14.12 Genesmall nuclear ribonucleoprotein polypeptide A' pseudogene |
RNU6-58P GeneRNA, U6 small nuclear 58, pseudogene |
RNU5E-9P GeneRNA, U5E small nuclear 9, pseudogene |
SNORD113-1 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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@ Genesmall nucleolar RNA, C/D box 114 cluster |
RNU7-73P GeneRNA, U7 small nuclear 73 pseudogene |
RNU6V GeneRNA, U6 small nuclear variant sequence with SNRPE pseudogene sequence |
SNORD58A Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U5E small nuclear 5, pseudogene |
SGTB Genesmall 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 Genesmall 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 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 10 |
SNRPGP15 Genesmall 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 GeneRNA, U1 small nuclear 17, pseudogene |
RNU2-2P GeneRNA, U2 small nuclear 2, pseudogene |
RNU5F-2P GeneRNA, U5F small nuclear 2, pseudogene |
RNU7-74P GeneRNA, U7 small nuclear 74 pseudogene |
RNU6-50P GeneRNA, U6 small nuclear 50, pseudogene |
SMIM3 Genesmall integral membrane protein 3 Enables identical protein binding activity. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM7 Genesmall integral membrane protein 7 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM6 Genesmall 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 Genesmall integral membrane protein 5 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM4 Genesmall 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 Genesmall integral membrane protein 9 Predicted to be located in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM8 Genesmall integral membrane protein 8 Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD115-36 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U5E small nuclear 2, pseudogene |
SNORD50A Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U6 small nuclear 82, pseudogene |
RNU1-24P GeneRNA, U1 small nuclear 24, pseudogene |
RNU7-43P GeneRNA, U7 small nuclear 43 pseudogene |
SNORA11E Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 66 pseudogene |
RNU6-19P GeneRNA, U6 small nuclear 19, pseudogene |
LOC100736412 Geneash2 (absent, small, or homeotic)-like (Drosophila) pseudogene |
SNORA69 Genesmall 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 GeneRNA, U4 small nuclear 3, pseudogene |
RNU6-16P GeneRNA, U6 small nuclear 16, pseudogene |
IMP3 GeneIMP3, 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 GeneIMP4, 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 9 pseudogene |
RNU7-82P GeneRNA, U7 small nuclear 82 pseudogene |
RNU7-17P GeneRNA, U7 small nuclear 17 pseudogene |
RNU105B GeneRNA, 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 GeneU2 small nuclear RNA auxiliary factor 1-like 4 pseudogene |
RNU6-6P GeneRNA, U6 small nuclear 6, pseudogene Predicted to be located in nuclear speck. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM10L2B Genesmall integral membrane protein 10 like 2B |
RNVU1-20 GeneRNA, 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 Geneash2 (absent, small, or homeotic)-like (Drosophila) pseudogene |
RNU4-1 GeneRNA, 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 GeneRNA, U7 small nuclear 37 pseudogene |
SNORA7B Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall nuclear ribonucleoprotein polypeptide B pseudogene |
SNORD116-30 Genesmall 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 GeneRNA, U7 small nuclear 18 pseudogene |
RNU86 GeneRNA, 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 Geneheat 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneKRR1, small subunit (SSU) processome component, homolog (yeast) pseudogene 1 |
RNU1-14P GeneRNA, U1 small nuclear 14, pseudogene |
SNORD116-28 Genesmall nucleolar RNA, C/D box 116-28 |
LOC150417 Genesmall nuclear ribonucleoprotein polypeptide A' pseudogene |
RNU6ATAC2P GeneRNA, U6atac small nuclear 2, pseudogene |
RNU5F-5P GeneRNA, U5F small nuclear 5, pseudogene |
SNRPA1 Genesmall 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 GeneUTP15, 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 Genesmall 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 GeneRNA, U7 small nuclear 71 pseudogene |
SNORA36B Genesmall 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 Genesmall 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 GeneRNA, 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 GeneRNA, U6 small nuclear 68, pseudogene |
RNU6-57P GeneRNA, U6 small nuclear 57, pseudogene |
SNORD115-18 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genecalpain, 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 Genecalpain, 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 Genesmall 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 Genesmall 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 Genesmall ILF3/NF90-associated RNA I |
LSM7 GeneLSM7 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 GeneLSM1, 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 GeneLSM2 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 GeneRNA, U6 small nuclear 72, pseudogene |
RNU5E-7P GeneRNA, U5E small nuclear 7, pseudogene |
RNU12 GeneRNA, 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 GeneRNA, 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 GeneRNA, U4 small nuclear 8, pseudogene |
RNU7-58P GeneRNA, U7 small nuclear 58 pseudogene |
RNU5A-7P GeneRNA, U5A small nuclear 7, pseudogene |
RNU7-23P GeneRNA, U7 small nuclear 23 pseudogene |
SNORD109A Genesmall 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 Genesmall 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 Genesmall 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 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 9 |
SNRPEP8 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 8 |
SNRPEP5 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 5 |
SNRPEP4 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 4 |
SNRPEP7 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 7 |
SNRPEP6 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 6 |
SNRPEP1 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 1 |
SNRPEP3 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 3 |
SNRPEP2 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 2 |
SNORA51 Genesmall 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 Genesmall 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 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 1 |
SCARNA13 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall ArfGAP2 Predicted to enable GTPase activator activity. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-89P GeneRNA, U7 small nuclear 89 pseudogene |
LOC101929087 Genesmall ubiquitin-related modifier 2-like |
SNORA45B Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall nucleolar RNA, C/D box 119 |
SNORD117 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 61 pseudogene |
SNORD11B Genesmall 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 GeneRNA, U7 small nuclear 63 pseudogene |
SNRPGP2 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 2 |
SNAR-C5 Genesmall ILF3/NF90-associated RNA C5 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-C4 Genesmall ILF3/NF90-associated RNA C4 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-C1 Genesmall ILF3/NF90-associated RNA C1 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNAR-C2 Genesmall ILF3/NF90-associated RNA C2 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU12-2P GeneRNA, U12 small nuclear 2, pseudogene |
SCARNA9 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall nuclear ribonucleoprotein polypeptide E pseudogene 10 |
RNU7-46P GeneRNA, U7 small nuclear 46 pseudogene |
SNORD36A Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, 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 Genesmall 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 GeneRNA, U6 small nuclear 35, pseudogene |
SNRPD2P2 Genesmall nuclear ribonucleoprotein D2 pseudogene 2 |
SNRPD2P1 Genesmall nuclear ribonucleoprotein D2 pseudogene 1 |
SNORD116-9 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 40 pseudogene |
RNU7-69P GeneRNA, U7 small nuclear 69 pseudogene |
RNU7-34P GeneRNA, U7 small nuclear 34 pseudogene |
SNORD19B Genesmall 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 GeneRNA, U5B small nuclear 4, pseudogene |
RNU7-55P GeneRNA, U7 small nuclear 55 pseudogene |
RNU5A-3P GeneRNA, U5A small nuclear 3, pseudogene |
SNORD21 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall nucleolar RNA, C/D box 25 |
SNORD24 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, 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 Geneash2 (absent, small, or homeotic)-like (Drosophila) pseudogene |
SNAR-A9 Genesmall ILF3/NF90-associated RNA A9 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-26P GeneRNA, U7 small nuclear 26 pseudogene |
SNAR-A1 Genesmall ILF3/NF90-associated RNA A1 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SNRPN Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genecalpain, small subunit 1 pseudogene 1 |
RNVU1-8 GeneRNA, 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 GeneRNA, 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 GeneRNA, 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 GeneRNA, 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 GeneRNA, variant U1 small nuclear 1 |
SNORA20 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall EDRK-rich factor 1A (telomeric) pseudogene 1 |
U2AF1 GeneU2 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 GeneU2 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 GeneRNA, U6 small nuclear 75, pseudogene |
SNORD56B Genesmall 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 GeneRNA, U5E small nuclear 4, pseudogene |
SNRPCP19 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 19 |
SNRPCP18 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 18 |
SNRPCP15 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 15 |
SNRPCP14 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 14 |
SNRPCP12 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 12 |
SNRPCP11 Genesmall nuclear ribonucleoprotein polypeptide C pseudogene 11 |
SNORD116-20 Genesmall 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 Genesmall 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 GeneRNA, U1 small nuclear 11, pseudogene |
RNU7-7P GeneRNA, U7 small nuclear 7 pseudogene |
LOC100130842 Genesmall integral membrane protein 7 pseudogene |
RNU6-81P GeneRNA, U6 small nuclear 81, pseudogene |
RNU7-76P GeneRNA, U7 small nuclear 76 pseudogene |
UTP23 GeneUTP23, 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 GeneUTP20, 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 GeneRNA, 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 Genesmall nuclear ribonucleoprotein polypeptide F pseudogene 4 |
SNRPFP2 Genesmall nuclear ribonucleoprotein polypeptide F pseudogene 2 |
SNRPFP1 Genesmall nuclear ribonucleoprotein polypeptide F pseudogene 1 |
SNHG10 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneM-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene |
RNU4-5P GeneRNA, U4 small nuclear 5, pseudogene |
SNRPGP3 Genesmall nuclear ribonucleoprotein polypeptide G pseudogene 3 |
LOC100129492 Genesmall nuclear ribonucleoprotein Sm D1 pseudogene |
SGSM2 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U4 small nuclear 10, pseudogene |
LOC101929240 GeneU5 small nuclear ribonucleoprotein 200 kDa helicase pseudogene |
RNU1-19P GeneRNA, U1 small nuclear 19, pseudogene |
RNU6-14P GeneRNA, U6 small nuclear 14, pseudogene |
RNU5F-8P GeneRNA, U5F small nuclear 8, pseudogene |
SNORD35A Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 45 pseudogene |
RNU7-84P GeneRNA, U7 small nuclear 84 pseudogene |
RNU6-30P GeneRNA, U6 small nuclear 30, pseudogene |
SNORD13P1 Genesmall nucleolar RNA, C/D box 13 pseudogene 1 |
SNORD13P3 Genesmall nucleolar RNA, C/D box 13 pseudogene 3 |
SNORD13P2 Genesmall nucleolar RNA, C/D box 13 pseudogene 2 |
RNU6-78P GeneRNA, U6 small nuclear 78, pseudogene |
LOC100422645 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase 2 pseudogene |
RNU7-39P GeneRNA, U7 small nuclear 39 pseudogene |
SNORD14E Genesmall nucleolar RNA, C/D box 14E |
SNORD14D Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 64 pseudogene |
LOC100533850 GeneM-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene |
RNU7-70P GeneRNA, U7 small nuclear 70 pseudogene |
SNORA37 Genesmall 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 GeneRNA, U7 small nuclear 56 pseudogene |
RNU5F-1 GeneRNA, 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 15 pseudogene |
RNU1-1 GeneRNA, 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 GeneRNA, 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 Genesmall ILF3/NF90-associated RNA H |
LOC100631375 GeneM-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein) pseudogene |
RNU6-59P GeneRNA, U6 small nuclear 59, pseudogene |
RNU7-31P GeneRNA, U7 small nuclear 31 pseudogene |
LOC105379766 Genesmall nuclear ribonucleoprotein-associated protein N-like |
SNORA5A Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U5B small nuclear 2, pseudogene |
RNU5E-3P GeneRNA, U5E small nuclear 3, pseudogene |
RNU7-50P GeneRNA, U7 small nuclear 50 pseudogene |
RNU5A-6P GeneRNA, U5A small nuclear 6, pseudogene |
SCARNA6 Genesmall 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 GeneRNA, U5E small nuclear 10, pseudogene |
SNORD116-19 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 29 pseudogene |
SNORD59B Genesmall 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 Genesmall 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 Genesmall nuclear ribonucleoprotein polypeptides B and B1 pseudogene 1 |
LOC100128056 GeneCTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) small phosphatase 2 pseudogene |
SNORD72 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 79 pseudogene |
RNU6-28P GeneRNA, U6 small nuclear 28, pseudogene |
SNRPFP3 Genesmall nuclear ribonucleoprotein polypeptide F pseudogene 3 |
RNU2-5P GeneRNA, U2 small nuclear 5, pseudogene |
SNORD56 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall nucleolar RNA, C/D box 113-2 |
SNORD96B Genesmall nucleolar RNA, C/D box 96B |
SNORD96A Genesmall nucleolar RNA, C/D box 96A |
RNU5F-3P GeneRNA, U5F small nuclear 3, pseudogene |
SNORD38B Genesmall 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 Genesmall 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 GeneLSM10, 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 GeneLSM11, 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 GeneRNA, U7 small nuclear 48 pseudogene |
SNORD115-34 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall nucleolar RNA host gene 21 |
SNHG22 Genesmall nucleolar RNA host gene 22 |
SNHG23 Genesmall nucleolar RNA host gene 23 |
SNHG24 Genesmall nucleolar RNA host gene 24 |
RNU6-42P GeneRNA, U6 small nuclear 42, pseudogene |
SNORD115@ Genesmall nucleolar RNA, C/D box 115 cluster |
SNORA59A Genesmall 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 Genesmall 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 Genesmall ubiquitin-like modifier 2 |
RNU7-21P GeneRNA, U7 small nuclear 21 pseudogene |
SNORD71 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 3 pseudogene |
SNORD6 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Geneash2 (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 GeneRNA, U7 small nuclear 2 pseudogene |
RNU2-7P GeneRNA, U2 small nuclear 7, pseudogene |
SMLR1 Genesmall leucine-rich protein 1 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SNORD114-8 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall proline-rich protein 2C (pseudogene) |
SPRR2B Genesmall 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 GeneRNA, U6 small nuclear 33, pseudogene |
LSM3 GeneLSM3 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 Genesmall 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 GeneRNA, U7 small nuclear 67 pseudogene |
CTDSPL2 GeneCTD (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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 Genesmall 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 GeneRNA, U7 small nuclear 83 pseudogene |
SNAR-A13 Genesmall ILF3/NF90-associated RNA A13 Predicted to be located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
RNU7-16P GeneRNA, U7 small nuclear 16 pseudogene |
UTP4 GeneUTP4 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 Genesmall 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 GeneUTP11 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 GeneUTP25 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 Genesmall 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 Genesmall 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 Genesmall integral membrane protein 41 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SCYGR4 Genesmall cysteine and glycine repeat containing 4 Predicted to be located in intermediate filament. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM36 Genesmall integral membrane protein 36 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM33 Genesmall integral membrane protein 33 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM40 Genesmall 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 Genesmall integral membrane protein 38 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SNHG32 Genesmall nucleolar RNA host gene 32 Predicted to enable double-stranded RNA binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM27 Genesmall integral membrane protein 27 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM29 Genesmall integral membrane protein 29 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM31 Genesmall integral membrane protein 31 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM35 Genesmall integral membrane protein 35 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM43 Genesmall 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 Genesmall 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 Genesmall integral membrane protein 45 Involved in neuron maturation. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM30 Genesmall 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 Genesmall nucleolar RNA host gene 25 |
SNHG28 Genesmall nucleolar RNA host gene 28 Enables RNA binding activity. [provided by Alliance of Genome Resources, Mar 2025] |
SNHG29 Genesmall 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 Genesmall nucleolar RNA host gene 30 |
RNU6-645P GeneRNA, U6 small nuclear 645, pseudogene |
SNORA17B Genesmall 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 Genesmall integral membrane protein 44 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SNORA63B Genesmall 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 Genesmall nucleolar RNA host gene 26 |
SPRR5 Genesmall proline rich protein 5 |
STRIT1 Genesmall 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 Genesmall cysteine and glycine repeat containing 6 Predicted to be located in intermediate filament. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM42 Genesmall integral membrane protein 42 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM47 Genesmall integral membrane protein 47 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SMIM32 Genesmall integral membrane protein 32 Predicted to be located in membrane. [provided by Alliance of Genome Resources, Mar 2025] |
SCYGR10 Genesmall 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 Gene40S 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 Genesmall cysteine and glycine repeat containing 1 |
SCYGR7 Genesmall cysteine and glycine repeat containing 7 |
SCYGR8 Genesmall cysteine and glycine repeat containing 8 |
SCYGR3 Genesmall cysteine and glycine repeat containing 3 |
SCYGR2 Genesmall cysteine and glycine repeat containing 2 |
SCYGR5 Genesmall cysteine and glycine repeat containing 5 |
LOC107983987 Genesmall integral membrane protein 34B |
SMIM39 Genesmall integral membrane protein 39 |
SMIM10L3 Genesmall integral membrane protein 10 like 3 |
SMIM46 Genesmall integral membrane protein 46 |
small distal femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the small distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Small Distal Femoral Epiphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Small Distal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
[Mpa1 <small>Dsmall>-Tyr(Et)2 <small>Dsmall>-Tic7 <small>Dsmall>-Tic9]OT Gene SetFrom 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. |
abnormality of the distal femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
irregular distal femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the irregular distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlargement of the distal femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the enlargement of the distal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Irregular Distal Femoral Epiphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Irregular Distal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Flat Distal Femoral Epiphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Flat Distal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Enlargement Of The Distal Femoral Epiphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Enlargement Of The Distal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
N-methyl-Phe-Lys-Pro-<small>Dsmall>-Cha-Cha-<small>Dsmall>-Arg-CO2H Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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. |
abnormality of femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
flat capital femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the flat capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
flattened femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the flattened femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
irregular femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the irregular femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
irregular capital femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the irregular capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the capital femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the femoral head Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
avascular necrosis of the capital femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the avascular necrosis of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cone-shaped capital femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the cone-shaped capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlargement of the proximal femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the enlargement of the proximal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the capital femoral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the capital femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Irregular Capital Femoral Epiphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Irregular Capital Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Aplasia/Hypoplasia Of The Capital Femoral Epiphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Aplasia/Hypoplasia Of The Capital Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Femoral Epiphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of The Epiphysis Of The Femoral Head Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Epiphysis Of The Femoral Head in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Flat Capital Femoral Epiphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Flat Capital Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Enlargement Of The Proximal Femoral Epiphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Enlargement Of The Proximal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Irregular Femoral Epiphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Irregular Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Stippling Of The Epiphysis Of The Distal Phalanx Of The Thumb Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Stippling Of The Epiphysis Of The Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
trapezoidal distal femoral condyles Gene SetFrom HPO Gene-Disease Associations genes associated with the trapezoidal distal femoral condyles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal femoral metaphyseal abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the distal femoral metaphyseal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
wide distal femoral metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the wide distal femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal femoral bowing Gene SetFrom HPO Gene-Disease Associations genes associated with the distal femoral bowing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Distal Femoral Bowing Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Femoral Bowing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Trapezoidal Distal Femoral Condyles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Trapezoidal Distal Femoral Condyles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Wide Distal Femoral Metaphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wide Distal Femoral Metaphysis 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 SetFrom 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. |
bracket epiphysis of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the bracket epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphysis of the proximal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of upper limb epiphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of upper limb epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cone-shaped epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the cone-shaped epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphysis of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the proximal tibial epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the proximal tibial epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the 1st metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
cone-shaped epiphysis of the 1st metacarpal Gene SetFrom HPO Gene-Disease Associations genes associated with the cone-shaped epiphysis of the 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the humeral epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the humeral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphysis of the proximal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphysis of the proximal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bracket epiphysis of the middle phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the bracket epiphysis of the middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the proximal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of lower limb epiphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of lower limb epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphysis of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of epiphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
flattened epiphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the flattened epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphysis of the middle phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphysis of the proximal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of limb epiphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of limb epiphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of vertebral epiphysis morphology Gene SetFrom 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. |
abnormality of the epiphysis of the proximal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
enlarged epiphysis of the middle phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the middle phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal long bone epiphysis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone epiphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thickened long bone epiphysis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thickened long bone epiphysis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
epiphysis Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue epiphysis in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Cone-Shaped Epiphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cone-Shaped Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Vertebral Epiphysis Morphology Gene SetFrom 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. |
Triangular Epiphysis Of The Middle Phalanx Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Triangular Epiphysis Of The Middle Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Triangular Epiphysis Of The Proximal Phalanx Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Triangular Epiphysis Of The Proximal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Epiphysis Morphology Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Epiphysis Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Cone-Shaped Epiphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cone-Shaped Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Flattened Epiphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Flattened Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
abnormal long bone epiphysis morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal long bone epiphysis morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thickened long bone epiphysis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thickened long bone epiphysis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Epiphysis Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Epiphysis in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; small cell carcinoma of lung; squamous cell carcinoma Gene SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom 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 SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Femoral Fractures from the curated CTD Gene-Disease Associations dataset. |
femoral neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease femoral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
femoral neck geometry Gene SetFrom GAD Gene-Disease Associations genes associated with the disease femoral neck geometry in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
femoral neck fractures; fractures, bone; osteoporosis, postmenopausal; spinal fractures Gene SetFrom 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. |
femoral neck fractures; fractures, stress Gene SetFrom 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. |
femoral neck fractures; osteoporosis; spinal injuries Gene SetFrom 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. |
carotid and femoral artery stiffness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carotid and femoral artery stiffness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
femoral Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term femoral in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Femoral neck bone geometry Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Femoral neck bone geometry phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Femoral neck bone geometry and menarche (age at onset) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Femoral neck bone geometry and menarche (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
abnormality of the femoral neck Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck or head region Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral neck or head region phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral head Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the femoral head phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of the femoral neck or head region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral neck or head region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
femoral hernia Gene SetFrom HPO Gene-Disease Associations genes associated with the femoral hernia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short femoral neck Gene SetFrom HPO Gene-Disease Associations genes associated with the short femoral neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad femoral neck Gene SetFrom HPO Gene-Disease Associations genes associated with the broad femoral neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multicentric ossification of proximal femoral epiphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the multicentric ossification of proximal femoral epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
femoral bowing Gene SetFrom HPO Gene-Disease Associations genes associated with the femoral bowing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
narrow femoral neck Gene SetFrom HPO Gene-Disease Associations genes associated with the narrow femoral neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
delayed femoral head ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the delayed femoral head ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
disproportionate prominence of the femoral medial condyle Gene SetFrom HPO Gene-Disease Associations genes associated with the disproportionate prominence of the femoral medial condyle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplasia of the femoral head Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplasia of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hyperplasia of the femoral trochanters Gene SetFrom HPO Gene-Disease Associations genes associated with the hyperplasia of the femoral trochanters phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification involving the femoral head and neck Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lateral displacement of the femoral head Gene SetFrom HPO Gene-Disease Associations genes associated with the lateral displacement of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal femoral epiphysiolysis Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal femoral epiphysiolysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
flared femoral metaphysis Gene SetFrom HPO Gene-Disease Associations genes associated with the flared femoral metaphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
flattened femoral head Gene SetFrom HPO Gene-Disease Associations genes associated with the flattened femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal femoral metaphyseal abnormality Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal femoral metaphyseal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lateral femoral bowing Gene SetFrom HPO Gene-Disease Associations genes associated with the lateral femoral bowing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
wide capital femoral epiphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the wide capital femoral epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
femoral bowing present at birth, straightening with time Gene SetFrom HPO Gene-Disease Associations genes associated with the femoral bowing present at birth, straightening with time phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia involving the femoral head and neck Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
proximal femoral metaphyseal irregularity Gene SetFrom HPO Gene-Disease Associations genes associated with the proximal femoral metaphyseal irregularity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral head Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad femoral metaphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the broad femoral metaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multicentric femoral head ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the multicentric femoral head ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the femoral neck Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the femoral neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dysplasia of the femoral head Gene SetFrom HPO Gene-Disease Associations genes associated with the dysplasia of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Femoral Neck Fractures Gene SetFrom 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. |
Femoral Fractures Gene SetFrom 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. |
abnormal femoral fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal femoral fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased femoral fat pad weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased femoral fat pad weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
avascular necrosis of the femoral head Gene SetFrom OMIM Gene-Disease Associations genes associated with the avascular necrosis of the femoral head phenotype from the curated OMIM Gene-Disease Associations dataset. |
femoral artery Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue femoral artery from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
femoral artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue femoral artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
femoral muscle Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue femoral muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Slipped Capital Femoral Epiphyses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Slipped Capital Femoral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Femoral Artery Occlusion Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Femoral Artery Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Superficial Femoral Artery Occlusion Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Superficial Femoral Artery Occlusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of The Femoral Metaphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Femoral Metaphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Proximal Femoral Metaphyseal Abnormality Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Proximal Femoral Metaphyseal Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Avascular Necrosis Of Femoral Head Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Avascular Necrosis Of Femoral Head in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Flared Femoral Metaphysis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Flared Femoral Metaphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Femoral Hypoplasia - Unusual Facies Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Femoral Hypoplasia - Unusual Facies Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Wide Capital Femoral Epiphyses Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Wide Capital Femoral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Broad Femoral Neck Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Femoral Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Excessive Femoral Anteversion Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Excessive Femoral Anteversion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Delayed Proximal Femoral Epiphyseal Ossification Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Proximal Femoral Epiphyseal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Femoral Neck Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Femoral Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Femoral Bowing Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Femoral Bowing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Proximal Femoral Metaphyseal Irregularity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Femoral Metaphyseal Irregularity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Atypical Femoral Fracture Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atypical Femoral Fracture in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Femoral Bowing Present At Birth, Straightening With Time Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Femoral Bowing Present At Birth, Straightening With Time in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Flattened Femoral Head Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Flattened Femoral Head in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Narrow Femoral Neck Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Narrow Femoral Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Early Ossification Of Capital Femoral Epiphyses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Early Ossification Of Capital Femoral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Delayed Femoral Head Ossification Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Femoral Head Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multicentric Femoral Head Ossification Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multicentric Femoral Head Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Multicentric Ossification Of Proximal Femoral Epiphyses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multicentric Ossification Of Proximal Femoral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Broad Femoral Metaphyses Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Femoral Metaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lateral Femoral Bowing Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lateral Femoral Bowing in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Ossification Involving The Femoral Head And Neck Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Ossification Involving The Femoral Head And Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dysplasia Of The Femoral Head Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dysplasia Of The Femoral Head in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Disproportionate Prominence Of The Femoral Medial Condyle Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Disproportionate Prominence Of The Femoral Medial Condyle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Femoral Neck Or Head Region Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Femoral Neck Or Head Region in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lateral Displacement Of The Femoral Head Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lateral Displacement Of The Femoral Head in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Wide Proximal Femoral Metaphysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wide Proximal Femoral Metaphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
decreased femoral compact bone area Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased femoral compact bone area phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased femoral compact bone area Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased femoral compact bone area phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased femoral fat pad weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased femoral fat pad weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Femoral cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Femoral cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Femoral neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Femoral neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Femoral vein thrombophlebitis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Femoral vein thrombophlebitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Femoral artery Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Femoral artery from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Femoral artery Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Femoral artery in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Femoral muscle Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Femoral muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Avascular necrosis of femoral head Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Avascular necrosis of femoral head phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Nontraumatic osteonecrosis of the femoral head Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Nontraumatic osteonecrosis of the femoral head phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Arterial stiffness (carotid-femoral pulse wave velocity) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Arterial stiffness (carotid-femoral pulse wave velocity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Arterial stiffness (brachial-femoral pulse wave velocity) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Arterial stiffness (brachial-femoral pulse wave velocity) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bone mineral density (femoral neck) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bone mineral density (femoral neck) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pediatric bone mineral content (femoral neck) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric bone mineral content (femoral neck) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Pediatric bone mineral density (femoral neck) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Pediatric bone mineral density (femoral neck) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Idiopathic osteonecrosis of the femoral head Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Idiopathic osteonecrosis of the femoral head phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Femoral neck bone mineral density Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Femoral neck bone mineral density phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Femoral neck bone mineral density and trunk fat mass adjusted by trunk lean mass Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Femoral neck bone mineral density and trunk fat mass adjusted by trunk lean mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Femoral neck length Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Femoral neck length phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Narrowest width of the femoral neck Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Narrowest width of the femoral neck phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Femoral neck section modulus Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Femoral neck section modulus phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Femoral neck bone geometry Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Femoral neck bone geometry phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Femoral neck bone geometry and menarche (age at onset) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Femoral neck bone geometry and menarche (age at onset) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Femoral neck size Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Femoral neck size phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bisphosphonate-associated atypical femoral fracture Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bisphosphonate-associated atypical femoral fracture phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Atypical femoral fracture in phosphonate treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Atypical femoral fracture in phosphonate treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Bone mineral density (femoral neck) in inflammatory bowel disease Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Bone mineral density (femoral neck) in inflammatory bowel disease phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Distal hereditary motor neuronopathy 2D Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy 2D phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, distal, autosomal dominant Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, distal, autosomal recessive Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal spinal muscular atrophy, X-linked 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, X-linked 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, distal, with normal red cell morphology Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, with normal red cell morphology phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 2A Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 2C Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 2B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal myopathy Markesbery-Griggs type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal myopathy Markesbery-Griggs type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, distal, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 5B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 5B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal arthrogryposis type 1B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal arthrogryposis type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 7B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 7B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Renal tubular acidosis, distal, with hemolytic anemia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, distal, with hemolytic anemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal hereditary motor neuronopathy type 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal hereditary motor neuronopathy type 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal arthrogryposis type 2B Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal arthrogryposis type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arthrogryposis, distal, type 5d Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arthrogryposis, distal, type 5d phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, distal, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, distal, 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, distal, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Distal spinal muscular atrophy, autosomal recessive 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Distal spinal muscular atrophy, autosomal recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, Distal, with Anterior Tibial Onset Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Distal, with Anterior Tibial Onset from the curated CTD Gene-Disease Associations dataset. |
Welander distal myopathy, Swedish type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Welander distal myopathy, Swedish type from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Distal Hereditary Motor, Type IIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type IIA from the curated CTD Gene-Disease Associations dataset. |
Renal Tubular Acidosis, Distal, With Hemolytic Anemia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Distal, With Hemolytic Anemia from the curated CTD Gene-Disease Associations dataset. |
Neuronopathy, Distal Hereditary Motor, Type V Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type V from the curated CTD Gene-Disease Associations dataset. |
Jacobsen Distal 11q Deletion Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Jacobsen Distal 11q Deletion Syndrome from the curated CTD Gene-Disease Associations dataset. |
Renal tubular acidosis, distal, autosomal recessive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal tubular acidosis, distal, autosomal recessive from the curated CTD Gene-Disease Associations dataset. |
Neuronopathy, Distal Hereditary Motor, Type IIB Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type IIB from the curated CTD Gene-Disease Associations dataset. |
Arthrogryposis, Distal, Type 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arthrogryposis, Distal, Type 4 from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset. |
ARTHROGRYPOSIS, DISTAL, TYPE 1A Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ARTHROGRYPOSIS, DISTAL, TYPE 1A from the curated CTD Gene-Disease Associations dataset. |
Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Distal, with Progressive Nerve Deafness from the curated CTD Gene-Disease Associations dataset. |
Distal myopathy, Nonaka type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Distal myopathy, Nonaka type from the curated CTD Gene-Disease Associations dataset. |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC from the curated CTD Gene-Disease Associations dataset. |
Neuropathy, Distal Hereditary Motor, Type VIIA Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuropathy, Distal Hereditary Motor, Type VIIA from the curated CTD Gene-Disease Associations dataset. |
Arthrogryposis multiplex congenita, distal, X-linked Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Arthrogryposis multiplex congenita, distal, X-linked from the curated CTD Gene-Disease Associations dataset. |
Distal Myopathies Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Distal Myopathies from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset. |
Neuronopathy, Distal Hereditary Motor, Type Viib Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neuronopathy, Distal Hereditary Motor, Type Viib from the curated CTD Gene-Disease Associations dataset. |
Spinal Muscular Atrophy, Distal, X-Linked 3 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, X-Linked 3 from the curated CTD Gene-Disease Associations dataset. |
Distal arthrogryposis type 2B Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Distal arthrogryposis type 2B from the curated CTD Gene-Disease Associations dataset. |
distal muscular dystrophy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal muscular dystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
distal hereditary motor neuropathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal hereditary motor neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
distal arthrogryposis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease distal arthrogryposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
familial distal renal tubular acidosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease familial distal renal tubular acidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
proximal chromosome 9p to q and distal chromosome 9q Gene SetFrom GAD Gene-Disease Associations genes associated with the disease proximal chromosome 9p to q and distal chromosome 9q in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
distal myopathies; myositis, inclusion body Gene SetFrom GAD Gene-Disease Associations genes associated with the disease distal myopathies; myositis, inclusion body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
distal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term distal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
proximal/distal pattern formation involved in nephron development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation involved in nephron development biological process from the curated GO Biological Process Annotations 2015 dataset. |
metanephric distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metanephric distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
proximal/distal pattern formation involved in metanephric nephron development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation involved in metanephric nephron development biological process from the curated GO Biological Process Annotations 2015 dataset. |
metanephric distal tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metanephric distal tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
metanephric distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the metanephric distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
distal tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the distal tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
lung proximal/distal axis specification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lung proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2015 dataset. |
polarity specification of proximal/distal axis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the polarity specification of proximal/distal axis biological process from the curated GO Biological Process Annotations 2015 dataset. |
proximal/distal axis specification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2015 dataset. |
proximal/distal pattern formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2015 dataset. |
rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in positive regulation of transcription Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in positive regulation of transcription molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
rna polymerase ii distal enhancer sequence-specific dna binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rna polymerase ii distal enhancer sequence-specific dna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in negative regulation of transcription Gene SetFrom GO Molecular Function Annotations 2015 genes performing the rna polymerase ii distal enhancer sequence-specific dna binding transcription factor activity involved in negative regulation of transcription molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
wide tufts of distal phalanges Gene SetFrom HPO Gene-Disease Associations genes associated with the wide tufts of distal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tapering pointed ends of distal finger phalanges Gene SetFrom HPO Gene-Disease Associations genes associated with the tapering pointed ends of distal finger phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal upper limb muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the distal upper limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
osteolytic defects of the distal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the osteolytic defects of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal widening of metacarpals Gene SetFrom HPO Gene-Disease Associations genes associated with the distal widening of metacarpals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
late-onset distal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the late-onset distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
impaired distal vibration sensation Gene SetFrom HPO Gene-Disease Associations genes associated with the impaired distal vibration sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad distal phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the broad distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of distal phalanx of toe Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial duplication of the distal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
impaired distal tactile sensation Gene SetFrom HPO Gene-Disease Associations genes associated with the impaired distal tactile sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of the distal phalanx of hand Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the epiphyses of the distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad distal phalanges of all fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the broad distal phalanges of all fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of the distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sclerosis of distal finger phalanx Gene SetFrom HPO Gene-Disease Associations genes associated with the sclerosis of distal finger phalanx phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial duplication of the distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dysplastic distal thumb phalanges with a central hole Gene SetFrom HPO Gene-Disease Associations genes associated with the dysplastic distal thumb phalanges with a central hole phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
widened distal phalanges Gene SetFrom HPO Gene-Disease Associations genes associated with the widened distal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) Gene SetFrom HPO Gene-Disease Associations genes associated with the osteomyelitis or necrosis, distal, due to sensory neuropathy (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial duplication of the distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad distal hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the broad distal hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent distal interphalangeal creases Gene SetFrom HPO Gene-Disease Associations genes associated with the absent distal interphalangeal creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
triangular shaped distal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the triangular shaped distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
slender distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the slender distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the broad distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal ulnar hypoplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the distal ulnar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive distal muscular atrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive distal muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal upper limb amyotrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the distal upper limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bifid distal phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the bifid distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal lower limb amyotrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the distal lower limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal lower limb muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the distal lower limb muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased distal sensory nerve action potential Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased distal sensory nerve action potential phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
aplasia/hypoplasia of the distal phalanx of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal tapering of metatarsals Gene SetFrom HPO Gene-Disease Associations genes associated with the distal tapering of metatarsals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal ileal atresia Gene SetFrom HPO Gene-Disease Associations genes associated with the distal ileal atresia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal tapering femur Gene SetFrom HPO Gene-Disease Associations genes associated with the distal tapering femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ivory epiphyses of the distal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the ivory epiphyses of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of the distal phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypoplastic distal humeri Gene SetFrom HPO Gene-Disease Associations genes associated with the hypoplastic distal humeri phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
complete duplication of the distal phalanges of the hand Gene SetFrom HPO Gene-Disease Associations genes associated with the complete duplication of the distal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad distal phalanx of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the broad distal phalanx of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal amyotrophy Gene SetFrom HPO Gene-Disease Associations genes associated with the distal amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
broad distal phalanx of the hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the broad distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the 3rd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal shortening of limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the distal shortening of limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
osteolytic defects of the distal phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the osteolytic defects of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal sensory impairment of all modalities Gene SetFrom HPO Gene-Disease Associations genes associated with the distal sensory impairment of all modalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
fifth finger distal phalanx clinodactyly Gene SetFrom HPO Gene-Disease Associations genes associated with the fifth finger distal phalanx clinodactyly phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of the distal phalanx of the hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
club-shaped distal femur Gene SetFrom HPO Gene-Disease Associations genes associated with the club-shaped distal femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanges of the toes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanges of the toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
shortening of all distal phalanges of the fingers Gene SetFrom HPO Gene-Disease Associations genes associated with the shortening of all distal phalanges of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal/middle symphalangism of 5th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the distal/middle symphalangism of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
long distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the long distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent distal phalanges Gene SetFrom HPO Gene-Disease Associations genes associated with the absent distal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal symphalangism Gene SetFrom HPO Gene-Disease Associations genes associated with the distal symphalangism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized distal tubular acidosis Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized distal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
partial duplication of the distal phalanx of the hallux Gene SetFrom HPO Gene-Disease Associations genes associated with the partial duplication of the distal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
bifid distal phalanx of toe Gene SetFrom HPO Gene-Disease Associations genes associated with the bifid distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypermobility of distal interphalangeal joints Gene SetFrom HPO Gene-Disease Associations genes associated with the hypermobility of distal interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of toe Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal renal tubular acidosis Gene SetFrom HPO Gene-Disease Associations genes associated with the distal renal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
short distal phalanx of the 4th finger Gene SetFrom HPO Gene-Disease Associations genes associated with the short distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal sensory impairment Gene SetFrom HPO Gene-Disease Associations genes associated with the distal sensory impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
duplication of the distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the duplication of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
progressive distal muscle weakness Gene SetFrom HPO Gene-Disease Associations genes associated with the progressive distal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
tapered distal phalanges of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the tapered distal phalanges of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal peripheral sensory neuropathy Gene SetFrom HPO Gene-Disease Associations genes associated with the distal peripheral sensory neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
complete duplication of distal phalanx of the thumb Gene SetFrom HPO Gene-Disease Associations genes associated with the complete duplication of distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
acroosteolysis of distal phalanges (feet) Gene SetFrom HPO Gene-Disease Associations genes associated with the acroosteolysis of distal phalanges (feet) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal tibial bowing Gene SetFrom HPO Gene-Disease Associations genes associated with the distal tibial bowing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal urethral duplication Gene SetFrom HPO Gene-Disease Associations genes associated with the distal urethral duplication phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal sensory loss of all modalities Gene SetFrom HPO Gene-Disease Associations genes associated with the distal sensory loss of all modalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal arthrogryposis Gene SetFrom HPO Gene-Disease Associations genes associated with the distal arthrogryposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the distal phalanx of the 2nd finger Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
distal symphalangism (hands) Gene SetFrom HPO Gene-Disease Associations genes associated with the distal symphalangism (hands) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
impaired distal proprioception Gene SetFrom HPO Gene-Disease Associations genes associated with the impaired distal proprioception phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent fourth finger distal interphalangeal crease Gene SetFrom HPO Gene-Disease Associations genes associated with the absent fourth finger distal interphalangeal crease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Distal-less-like homeobox protein, N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Distal-less-like homeobox protein, N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
dilated distal convoluted tubules Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated distal convoluted tubules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal distal convoluted tubule morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal distal convoluted tubule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal distal visceral endoderm morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal distal visceral endoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal proximal-distal axis patterning Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal proximal-distal axis patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent distal visceral endoderm Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent distal visceral endoderm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
chromosome 7q11.23 deletion syndrome, distal, 1.2mb Gene SetFrom OMIM Gene-Disease Associations genes associated with the chromosome 7q11.23 deletion syndrome, distal, 1.2mb phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuronopathy, distal hereditary motor, type vi Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type vi phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, autosomal recessive, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, autosomal recessive, 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, autosomal recessive, 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, distal, 4 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, distal, 4 phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuronopathy, distal hereditary motor, type vb Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type vb phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuronopathy, distal hereditary motor, type viia Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type viia phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 5 Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, chronic distal, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, chronic distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuronopathy, distal hereditary motor, type iid Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuronopathy, distal hereditary motor, type iid phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthyrgryposis, distal, type 2b Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthyrgryposis, distal, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset. |
chromosome 22q11.2 deletion syndrome, distal Gene SetFrom OMIM Gene-Disease Associations genes associated with the chromosome 22q11.2 deletion syndrome, distal phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, jerash type Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, jerash type phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 2b Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 2a Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 2a phenotype from the curated OMIM Gene-Disease Associations dataset. |
welander distal myopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the welander distal myopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
renal tubular acidosis, distal, ar Gene SetFrom OMIM Gene-Disease Associations genes associated with the renal tubular acidosis, distal, ar phenotype from the curated OMIM Gene-Disease Associations dataset. |
renal tubular acidosis, distal, ad Gene SetFrom OMIM Gene-Disease Associations genes associated with the renal tubular acidosis, distal, ad phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, distal 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, distal 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
laing distal myopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the laing distal myopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
?neuronopathy, distal hereditary motor, type iic Gene SetFrom OMIM Gene-Disease Associations genes associated with the ?neuronopathy, distal hereditary motor, type iic phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, type va Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type va phenotype from the curated OMIM Gene-Disease Associations dataset. |
renal tubular acidosis, distal, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the renal tubular acidosis, distal, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis multiplex congenita, distal, type 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis multiplex congenita, distal, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis multiplex congenita, distal, type 2b Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis multiplex congenita, distal, type 2b phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, distal, with anterior tibial onset Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, distal, with anterior tibial onset phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, x-linked 3 Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, x-linked 3 phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, type viib Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type viib phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 1b Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 1b phenotype from the curated OMIM Gene-Disease Associations dataset. |
spinal muscular atrophy, distal, congenital nonprogressive Gene SetFrom OMIM Gene-Disease Associations genes associated with the spinal muscular atrophy, distal, congenital nonprogressive phenotype from the curated OMIM Gene-Disease Associations dataset. |
arthrogryposis, distal, type 5d Gene SetFrom OMIM Gene-Disease Associations genes associated with the arthrogryposis, distal, type 5d phenotype from the curated OMIM Gene-Disease Associations dataset. |
myopathy, distal, tateyama type Gene SetFrom OMIM Gene-Disease Associations genes associated with the myopathy, distal, tateyama type phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, type iib Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type iib phenotype from the curated OMIM Gene-Disease Associations dataset. |
neuropathy, distal hereditary motor, type iia Gene SetFrom OMIM Gene-Disease Associations genes associated with the neuropathy, distal hereditary motor, type iia phenotype from the curated OMIM Gene-Disease Associations dataset. |
distal tip Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue distal tip in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
distal tubular epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue distal tubular epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
renal distal tubule Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue renal distal tubule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
distal tip cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue distal tip cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Distal Amyotrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Arthrogryposis Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Arthrogryposis Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Lower Limb Amyotrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Lower Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Jacobsen Distal 11Q Deletion Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Jacobsen Distal 11Q Deletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Spinal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Renal Tubular Acidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Renal Tubular Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Progressive Distal Muscular Atrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Progressive Distal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Monosomy 3P Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Monosomy 3P Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Periodic Paralysis With Later-Onset Distal Motor Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Periodic Paralysis With Later-Onset Distal Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Broad Distal Phalanges Of All Fingers Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Broad Distal Phalanges Of All Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chromosome 22Q11.2 Deletion Syndrome, Distal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 22Q11.2 Deletion Syndrome, Distal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Complete Duplication Of Distal Phalanx Of The Thumb Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Complete Duplication Of Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Short Distal Phalanx Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Short Distal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Fifth Finger Distal Phalanx Clinodactyly Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Fifth Finger Distal Phalanx Clinodactyly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Welander Distal Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Welander Distal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Upper Limb Amyotrophy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Upper Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Ileal Obstruction Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Ileal Obstruction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Intestinal Obstruction Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Intestinal Obstruction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Tibial Bowing Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Tibial Bowing in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Bile Duct Cancer Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Bile Duct Cancer in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Aortic Dissection Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Aortic Dissection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Tapering Pointed Ends Of Distal Finger Phalanges Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Tapering Pointed Ends Of Distal Finger Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Hereditary Motor Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Hereditary Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Triangular Shaped Distal Phalanx Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Triangular Shaped Distal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Peripheral Sensory Neuropathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Peripheral Sensory Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bifid Distal Phalanx Of Toe Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bifid Distal Phalanx Of Toe in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Arthrogryposis Type 5D Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Arthrogryposis Type 5D in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Monosomy 12P Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Monosomy 12P in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Partial Duplication Of The Distal Phalanx Of The 2Nd Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Partial Duplication Of The Distal Phalanx Of The 2Nd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Partial Duplication Of The Distal Phalanx Of The 3Rd Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Partial Duplication Of The Distal Phalanx Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Tapering Femur Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Tapering Femur in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Generalized Distal Tubular Acidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Generalized Distal Tubular Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Colitis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Colitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Urethral Duplication Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Urethral Duplication in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Dysplastic Distal Thumb Phalanges With A Central Hole Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Dysplastic Distal Thumb Phalanges With A Central Hole in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Broad Distal Phalanx Of The Hallux Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Broad Distal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Long Distal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Long Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Klhl9-Related Early-Onset Distal Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Klhl9-Related Early-Onset Distal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Bile Duct Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Bile Duct Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Complete Duplication Of The Distal Phalanges Of The Hand Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Complete Duplication Of The Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Acroosteolysis Of Distal Phalanges (Feet) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Acroosteolysis Of Distal Phalanges (Feet) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Curved Distal Phalanges Of The Hand Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Curved Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Myopathy 1 Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Myopathy 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Tapering Of Metatarsals Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Tapering Of Metatarsals in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Trisomy 10Q Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Trisomy 10Q Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Absent Fourth Finger Distal Interphalangeal Crease Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Absent Fourth Finger Distal Interphalangeal Crease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hyperkalemic Distal Renal Tubular Acidosis Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hyperkalemic Distal Renal Tubular Acidosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal-Type Epithelioid Sarcoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal-Type Epithelioid Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease B-Cell Immunodeficiency, Distal Limb Anomalies, And Urogenital Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Bullet-Shaped Distal Phalanx Of The Hallux Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Bullet-Shaped Distal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Ivory Epiphyses Of The Distal Phalanges Of The Hand Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Ivory Epiphyses Of The Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Adult-Onset Distal Myopathy Due To Valosin Containing Protein Mutation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal 17P13.3 Microdeletion Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal 17P13.3 Microdeletion Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Monosomy 1Q Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Monosomy 1Q in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Monosomy 13Q Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Distal Monosomy 13Q Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Chromosome 19Q13.11 Deletion Syndrome, Distal Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Chromosome 19Q13.11 Deletion Syndrome, Distal in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Distal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Sensory Impairment Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Sensory Impairment in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Short Distal Phalanx Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Distal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Impaired Distal Proprioception Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impaired Distal Proprioception in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Muscle Atrophy Due To Neurologic Disease Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Muscle Atrophy Due To Neurologic Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Shortening Of All Distal Phalanges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Shortening Of All Distal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fatigable Weakness Of Distal Limb Muscles Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatigable Weakness Of Distal Limb Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Late-Onset Distal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Late-Onset Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Lower Limb Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Lower Limb Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Upper Limb Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Upper Limb Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Broad Distal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Club-Shaped Distal Femur Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Club-Shaped Distal Femur in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Sensory Impairment Of All Modalities Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Sensory Impairment Of All Modalities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Renal Tubular Acidosis Co-Occurrent With Sensorineural Deafness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Renal Tubular Acidosis Co-Occurrent With Sensorineural Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Osteolytic Defects Of The Distal Phalanges Of The Hand Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Osteolytic Defects Of The Distal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Bifid Distal Phalanx Of The Thumb Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Bifid Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Partial Duplication Of The Distal Phalanx Of The Hallux Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Duplication Of The Distal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Impaired Distal Vibration Sensation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impaired Distal Vibration Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Progressive Distal Muscle Weakness Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Distal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Wide Tufts Of Distal Phalanges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wide Tufts Of Distal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hypermobility Of Distal Interphalangeal Joints Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypermobility Of Distal Interphalangeal Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Joint Laxity Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Joint Laxity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of The Distal Phalanx Of The Thumb Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Impaired Distal Tactile Sensation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Impaired Distal Tactile Sensation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Ileal Atresia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Ileal Atresia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Tapered Distal Phalanges Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tapered Distal Phalanges Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Duplication Of The Distal Phalanx Of Hand Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Duplication Of The Distal Phalanx Of Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Broad Distal Hallux Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Distal Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Broad Distal Phalanx Of The Thumb Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Distal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Widened Distal Phalanges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Widened Distal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Shortening Of Limbs Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Shortening Of Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Distal Interphalangeal Creases Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Distal Interphalangeal Creases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Slender Distal Phalanx Of Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slender Distal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Acroosteolysis Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Acroosteolysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Decreased Distal Sensory Nerve Action Potential Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Distal Sensory Nerve Action Potential in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Ulnar Hypoplasia Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Ulnar Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal Widening Of Metacarpals Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Widening Of Metacarpals in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Distal Phalanges Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Distal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Distal/Middle Symphalangism Of 5Th Finger Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal/Middle Symphalangism Of 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
proximal/distal pattern formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
proximal/distal axis specification Gene SetFrom GO Biological Process Annotations 2023 genes participating in the proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2023 dataset. |
metanephric distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the metanephric distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
metanephric distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the metanephric distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2023 dataset. |
metanephric distal tubule development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the metanephric distal tubule development biological process from the curated GO Biological Process Annotations 2023 dataset. |
distal tubule development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the distal tubule development biological process from the curated GO Biological Process Annotations 2023 dataset. |
distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2023 genes participating in the distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset. |
distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2023 dataset. |
distal dendrite Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the distal dendrite cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
apical distal dendrite Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the apical distal dendrite cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
dilated distal convoluted tubule Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated distal convoluted tubule phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal distal convoluted tubule morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal distal convoluted tubule morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal proximal-distal axis patterning Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal proximal-distal axis patterning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal distal visceral endoderm morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal distal visceral endoderm morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent distal visceral endoderm Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent distal visceral endoderm phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased distal limb length Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased distal limb length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Human - Kidney - L1 - Distal Convoluted Tubule Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L1 - Distal Convoluted Tubule cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L2 - Distal Convoluted Tubule Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Distal Convoluted Tubule cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Distal Convoluted Tubule Type 1 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Distal Convoluted Tubule Type 1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Human - Kidney - L3 - Distal Convoluted Tubule Type 2 Gene SetFrom HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Distal Convoluted Tubule Type 2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset. |
Distal epithelial cell_Distal airway_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal epithelial cell_Distal airway_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal Proliferative Progenitor cell_Bone_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal Proliferative Progenitor cell_Bone_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal limb bud cell_Limb bud_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal limb bud cell_Limb bud_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Enterocyte distal cell_Intestine_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Enterocyte distal cell_Intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal cell_Epithelium_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal stem cell_Epithelium_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal stem cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal convoluted tubular cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal convoluted tubular cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal tubule & loop of Henle cell_Fetal kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal tubule & loop of Henle cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal tubular cell_Fetal kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal tubular cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Medial and distal segment cell_Fetal kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Medial and distal segment cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal tubular cell_Kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal tubular cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal tubular cell_Kidney_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal tubular cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal convoluted tubular cell_Kidney_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal convoluted tubular cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal cell_Blood vessel_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal cell_Blood vessel_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal lung progenitor cell_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal lung progenitor cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal epithelial cell_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal epithelial cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal cell_Prostate_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal cell_Prostate_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Distal convoluted tubular cell_Epithelium_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Distal convoluted tubular cell_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
16p11 2 distal deletion syndrome Gene SetFrom WikiPathways Pathways 2024 proteins participating in the 16p11 2 distal deletion syndrome pathway from the WikiPathways Pathways 2024 dataset. |
7q11 23 distal copy number variation Gene SetFrom WikiPathways Pathways 2024 proteins participating in the 7q11 23 distal copy number variation pathway from the WikiPathways Pathways 2024 dataset. |
Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA) Gene Setproteins participating in the Defective SLC4A1 causes hereditary spherocytosis type 4 (HSP4), distal renal tubular acidosis (dRTA) and dRTA with hemolytic anemia (dRTA-HA) pathway from the Reactome Pathways 2024 dataset. |
Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5619114 Gene Setproteins participating in the Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5619114 pathway from the Reactome Pathways 2024 dataset. |
Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5658471 Gene Setproteins participating in the Defective SLC5A7 causes distal hereditary motor neuronopathy 7A (HMN7A)_5658471 pathway from the Reactome Pathways 2024 dataset. |
proximal/distal pattern formation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2025 dataset. |
proximal/distal axis specification Gene SetFrom GO Biological Process Annotations 2025 genes participating in the proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2025 dataset. |
metanephric distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the metanephric distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
metanephric distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the metanephric distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2025 dataset. |
metanephric distal tubule development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the metanephric distal tubule development biological process from the curated GO Biological Process Annotations 2025 dataset. |
distal tubule development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the distal tubule development biological process from the curated GO Biological Process Annotations 2025 dataset. |
distal tubule morphogenesis Gene SetFrom GO Biological Process Annotations 2025 genes participating in the distal tubule morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset. |
distal convoluted tubule development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the distal convoluted tubule development biological process from the curated GO Biological Process Annotations 2025 dataset. |
distal dendrite Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the distal dendrite cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
apical distal dendrite Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the apical distal dendrite cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
Distal arthrogryposis Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal arthrogryposis from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant distal hereditary motor neuronopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 5 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant distal hereditary motor neuronopathy 5 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal arthrogryposis type 1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal arthrogryposis type 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal myopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal myopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive distal hereditary motor neuronopathy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive distal hereditary motor neuronopathy from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2B Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal arthrogryposis type 2B from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal 10q deletion syndrome Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal 10q deletion syndrome from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal myopathy 1 Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Distal myopathy 1 from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Distal arthrogryposis type 5D Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 5D in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy with rimmed vacuoles Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy with rimmed vacuoles in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with dysmorphic facies and distal limb anomalies in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy with anterior tibial onset Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy with anterior tibial onset in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2B Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 14 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Chromosome 22q11.2 deletion syndrome, distal Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chromosome 22q11.2 deletion syndrome, distal in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 9 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
X-linked distal spinal muscular atrophy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked distal spinal muscular atrophy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 1B Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1B in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 10 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 1A Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1A in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant distal hereditary motor neuronopathy 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant distal hereditary motor neuronopathy 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 1C Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 1C in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 7 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Partial trisomy distal 4q Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Partial trisomy distal 4q in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal 10q deletion syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal 10q deletion syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal myopathy 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal myopathy 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 5 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 5 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 4 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 6 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 6 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive distal hereditary motor neuronopathy 8 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive distal hereditary motor neuronopathy 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2B2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2B1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Distal arthrogryposis type 2B3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Distal arthrogryposis type 2B3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Renal distal tubule Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Renal distal tubule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Distal tip cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Distal tip cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Distal tip Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Distal tip in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Distal tubular epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Distal tubular epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Distal axon Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Distal axon cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Distal portion of axoneme Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Distal portion of axoneme cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Distal dendrite Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Distal dendrite cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Apical distal dendrite Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Apical distal dendrite cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Photoreceptor distal connecting cilium Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Photoreceptor distal connecting cilium cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Distal axon Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Distal axon cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Distal dendrite Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Distal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Photoreceptor distal connecting cilium Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Photoreceptor distal connecting cilium cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Distal portion of axoneme Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Distal portion of axoneme cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Basal distal dendrite Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Basal distal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Apical distal dendrite Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Apical distal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
bacterial-type flagellum basal body, distal rod, L ring Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the bacterial-type flagellum basal body, distal rod, L ring cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
bacterial-type flagellum basal body, distal rod Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the bacterial-type flagellum basal body, distal rod cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Distal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive distal renal tubular acidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive distal renal tubular acidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive distal muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive distal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal recessive distal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
X-linked distal spinal muscular atrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked distal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal renal tubular acidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal renal tubular acidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal arthrogryposis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal arthrogryposis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal lower limb muscle weakness Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal lower limb muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal lower limb amyotrophy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal lower limb amyotrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal hereditary motor neuropathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal hereditary motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant distal renal tubular acidosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant distal renal tubular acidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Progressive scapulohumeroperoneal distal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive scapulohumeroperoneal distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Arthrogryposis multiplex congenita distal Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Arthrogryposis multiplex congenita distal phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Welander distal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Welander distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal shortening of limbs Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Distal shortening of limbs phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Finnish upper limb-onset distal myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Finnish upper limb-onset distal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Distal/Left-sided colorectal cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Distal/Left-sided colorectal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Distal colorectal cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Distal colorectal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
PMC8104016-hcg-12-e002353-s006.xlsx-mTHP-1-LPS_Prom-Distal-RefSeq_Name_IRF6 Gene SetFrom Rummagene Transcription Factor Associations 2026 target genes of the PMC8104016-hcg-12-e002353-s006.xlsx-mTHP-1-LPS_Prom-Distal-RefSeq_Name_IRF6 transcription factor from the Rummagene Transcription Factor Associations 2026 dataset. |
Non-small cell lung cancer Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Non-small cell lung cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Brain small vessel disease with hemorrhage Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Brain small vessel disease with hemorrhage phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Congenital sensory neuropathy with selective loss of small myelinated fibers Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Congenital sensory neuropathy with selective loss of small myelinated fibers phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
mitochondrial small ribosomal subunit Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the mitochondrial small ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
preribosome, small subunit precursor Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the preribosome, small subunit precursor cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
small nuclear ribonucleoprotein complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the small nuclear ribonucleoprotein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
small nucleolar ribonucleoprotein complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the small nucleolar ribonucleoprotein complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
organellar small ribosomal subunit Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the organellar small ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
small ribosomal subunit Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the small ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
gamma-tubulin small complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the gamma-tubulin small complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cytosolic small ribosomal subunit Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cytosolic small ribosomal subunit cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
small-subunit processome Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the small-subunit processome cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
mitochondrial small ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitochondrial small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
preribosome, small subunit precursor Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the preribosome, small subunit precursor cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
small nuclear ribonucleoprotein complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the small nuclear ribonucleoprotein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
small nucleolar ribonucleoprotein complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the small nucleolar ribonucleoprotein complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
chloroplast small ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the chloroplast small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
organellar small ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the organellar small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
small ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
gamma-tubulin small complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the gamma-tubulin small complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cytosolic small ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cytosolic small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
plastid small ribosomal subunit Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the plastid small ribosomal subunit cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
small-subunit processome Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the small-subunit processome cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
SNAPc (small nuclear RNA-activating protein) complex Gene Setproteins in the SNAPc (small nuclear RNA-activating protein) complex protein complex from the CORUM Protein Complexes dataset. |
Carcinoma, Small Cell Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carcinoma, Small Cell from the curated CTD Gene-Disease Associations dataset. |
Brain Small Vessel Disease with Hemorrhage Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Brain Small Vessel Disease with Hemorrhage from the curated CTD Gene-Disease Associations dataset. |
Carcinoma, Non-Small-Cell Lung Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Carcinoma, Non-Small-Cell Lung from the curated CTD Gene-Disease Associations dataset. |
Small Cell Lung Carcinoma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Small Cell Lung Carcinoma from the curated CTD Gene-Disease Associations dataset. |
Desmoplastic Small Round Cell Tumor Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Desmoplastic Small Round Cell Tumor from the curated CTD Gene-Disease Associations dataset. |
Carcinoma, Non-Small-Cell Lung Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Carcinoma, Non-Small-Cell Lung in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
non-small cell lung carcinoma Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease non-small cell lung carcinoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
small intestine cancer Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease small intestine cancer in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
ureter small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ureter small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small cell osteogenic sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small cell osteogenic sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine neuroendocrine neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine neuroendocrine neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
prostate small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease prostate small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gallbladder small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gallbladder small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine leiomyoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine leiomyoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lung combined type small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lung combined type small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
laryngeal small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease laryngeal small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lung mixed small cell and squamous cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lung mixed small cell and squamous cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine leiomyosarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine leiomyosarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hypercalcemic type ovarian small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hypercalcemic type ovarian small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine lymphoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine lymphoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gastric small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastric small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small cell sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small cell sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
non-small cell lung carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease non-small cell lung carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine adenocarcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ovarian small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ovarian small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestinal sarcoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestinal sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cervix small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cervix small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
endometrial small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease endometrial small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lung small cell carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lung small cell carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small intestine cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease small intestine cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
urinary bladder small cell neuroendocrine carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease urinary bladder small cell neuroendocrine carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
small for gestational age infant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease small for gestational age infant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, non-small-cell lung; exanthema; lung neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; exanthema; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; head and neck neoplasms; lung neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, small cell; carcinoma, squamous cell; head and neck neoplasms; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; chromosome aberrations; chromosome abnormality; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; lung neoplasms; lymphatic metastasis; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; lung neoplasms; lymphatic metastasis; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, non-small-cell lung; lung neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, non-small-cell lung; lung neoplasms; neoplasm metastasis; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; neoplasm metastasis; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, non-small-cell lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
non-small-cell lung cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease non-small-cell lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, non-small-cell lung; colorectal neoplasms; genitourinary neoplasms; lung neoplasms; neoplasm of lung ; neutropenia; urogenital neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; colorectal neoplasms; genitourinary neoplasms; lung neoplasms; neoplasm of lung ; neutropenia; urogenital neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; lung neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cerebral small-vessel disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cerebral small-vessel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
non-small cell lung carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease non-small cell lung carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
stroke, lacunar; small-vessel disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease stroke, lacunar; small-vessel disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
small artery compliance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease small artery compliance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; colorectal neoplasms; head and neck neoplasms; lung neoplasms; neoplasm of lung ; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; colorectal neoplasms; head and neck neoplasms; lung neoplasms; neoplasm of lung ; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cachexia; carcinoma, non-small-cell lung; gastrointestinal neoplasms; lung neoplasms; neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cachexia; carcinoma, non-small-cell lung; gastrointestinal neoplasms; lung neoplasms; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
non-small cell lung cancer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease non-small cell lung cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; esophageal neoplasms; lung neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; esophageal neoplasms; lung neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, non-small-cell lung; diarrhea; exanthema; head and neck neoplasms; lung neoplasms; neoplasms, squamous cell; ovarian neoplasms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; diarrhea; exanthema; head and neck neoplasms; lung neoplasms; neoplasms, squamous cell; ovarian neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
neuropathy, small fiber Gene SetFrom GAD Gene-Disease Associations genes associated with the disease neuropathy, small fiber in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
carcinoma, non-small-cell lung; lung neoplasms; pleural effusion, malignant Gene SetFrom GAD Gene-Disease Associations genes associated with the disease carcinoma, non-small-cell lung; lung neoplasms; pleural effusion, malignant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, giant cell; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm recurrence, local Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, giant cell; carcinoma, large cell; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm recurrence, local in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
vasculitis, antineutrophil cytoplasmic; antibodies-associated small vessel Gene SetFrom GAD Gene-Disease Associations genes associated with the disease vasculitis, antineutrophil cytoplasmic; antibodies-associated small vessel in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; carcinoma, non-small-cell lung; carcinoma, squamous cell; lung neoplasms; neoplasm of lung ; squamous cell carcinoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
small for gestational age Gene SetFrom GAD Gene-Disease Associations genes associated with the disease small for gestational age in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
differential expansion rates of small abdominal aortic aneurysms Gene SetFrom GAD Gene-Disease Associations genes associated with the disease differential expansion rates of small abdominal aortic aneurysms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adenocarcinoma; adenocarcinoma, bronchiolo-alveolar; adenocarcinoma, mucinous; carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adenocarcinoma; adenocarcinoma, bronchiolo-alveolar; adenocarcinoma, mucinous; carcinoma, non-small-cell lung; lung neoplasms; neoplasm of lung in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
small Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term small in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
Adenoma of small intestine_Intestinal Epithelium_GSE422 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during Adenoma of small intestine_Intestinal Epithelium_GSE422 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
B-cell chronic lymphocytic leukaemia-small lymphocytic lymphoma_Peripheral blood mononuclear cell_GSE8835 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Diseases genes differentially expressed during B-cell chronic lymphocytic leukaemia-small lymphocytic lymphoma_Peripheral blood mononuclear cell_GSE8835 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset. |
PLAGL2_deficiency_GDS3010_139_mouse_embryonic small intestine Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PLAGL2_deficiency_GDS3010_139_mouse_embryonic small intestine gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
PDX1_KO_GDS4348_360_mouse_Proximal small intestine Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PDX1_KO_GDS4348_360_mouse_Proximal small intestine gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
PTEN_KD_GDS2958_100_human_HCC827 - NON-SMALL CELL LUNG carcinoma cell line Gene SetFrom GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the PTEN_KD_GDS2958_100_human_HCC827 - NON-SMALL CELL LUNG carcinoma cell line gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset. |
amoxicillin_rattus norvegicus_gpl341_distal small intestine_gds1273 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the amoxicillin_rattus norvegicus_gpl341_distal small intestine_gds1273 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset. |
amoxicillin_rattus norvegicus_gpl341_proximal small intestine_gds1273 Gene SetFrom GEO Signatures of Differentially Expressed Genes for Small Molecules genes differentially expressed following the amoxicillin_rattus norvegicus_gpl341_proximal small intestine_gds1273 small molecule perturbation from the GEO Signatures of Differentially Expressed Genes for Small Molecules dataset. |
regulation of small gtpase mediated signal transduction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of small gtpase mediated signal transduction biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of small gtpase mediated signal transduction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of small gtpase mediated signal transduction biological process from the curated GO Biological Process Annotations 2015 dataset. |
small molecule catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the small molecule catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein modification by small protein conjugation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2015 dataset. |
ribosomal small subunit biogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ribosomal small subunit biogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of small gtpase mediated signal transduction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of small gtpase mediated signal transduction biological process from the curated GO Biological Process Annotations 2015 dataset. |
production of small rna involved in gene silencing by rna Gene SetFrom GO Biological Process Annotations 2015 genes participating in the production of small rna involved in gene silencing by rna biological process from the curated GO Biological Process Annotations 2015 dataset. |
nucleobase-containing small molecule catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the nucleobase-containing small molecule catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of production of small rna involved in gene silencing by rna Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of production of small rna involved in gene silencing by rna biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
small gtpase mediated signal transduction Gene SetFrom GO Biological Process Annotations 2015 genes participating in the small gtpase mediated signal transduction biological process from the curated GO Biological Process Annotations 2015 dataset. |
small molecule biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the small molecule biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
nucleobase-containing small molecule interconversion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the nucleobase-containing small molecule interconversion biological process from the curated GO Biological Process Annotations 2015 dataset. |
small rna loading onto risc Gene SetFrom GO Biological Process Annotations 2015 genes participating in the small rna loading onto risc biological process from the curated GO Biological Process Annotations 2015 dataset. |
ribosomal small subunit export from nucleus Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ribosomal small subunit export from nucleus biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
small nucleolar ribonucleoprotein complex assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the small nucleolar ribonucleoprotein complex assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
nucleobase-containing small molecule metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the nucleobase-containing small molecule metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
small molecule metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the small molecule metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
ribosomal small subunit assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ribosomal small subunit assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein modification by small protein removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein modification by small protein removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein modification by small protein conjugation or removal Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein modification by small protein conjugation or removal biological process from the curated GO Biological Process Annotations 2015 dataset. |
mitochondrial small ribosomal subunit Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the mitochondrial small ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
preribosome, small subunit precursor Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the preribosome, small subunit precursor cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
small nuclear ribonucleoprotein complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the small nuclear ribonucleoprotein complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
small nucleolar ribonucleoprotein complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the small nucleolar ribonucleoprotein complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
organellar small ribosomal subunit Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the organellar small ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
small ribosomal subunit Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the small ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
gamma-tubulin small complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the gamma-tubulin small complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
cytosolic small ribosomal subunit Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the cytosolic small ribosomal subunit cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
small-subunit processome Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the small-subunit processome cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
small molecule binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the small molecule binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
small gtpase binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the small gtpase binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
small conductance calcium-activated potassium channel activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the small conductance calcium-activated potassium channel activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
small protein activating enzyme binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the small protein activating enzyme binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
small gtpase regulator activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the small gtpase regulator activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
ribosomal small subunit binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the ribosomal small subunit binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
small protein activating enzyme activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the small protein activating enzyme activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
small ribosomal subunit rrna binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the small ribosomal subunit rrna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
small intestine Gene SetFrom GTEx Tissue Gene Expression Profiles genes with high or low expression in small intestine relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset. |
Response to irinotecan in non-small-cell lung cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Response to irinotecan in non-small-cell lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Non-small cell lung cancer (survival) Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Non-small cell lung cancer (survival) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Non-small cell lung cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Non-small cell lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Response to platinum-based chemotherapy in non-small-cell lung cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Response to platinum-based chemotherapy in non-small-cell lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Response to irinotecan and platinum-based chemotherapy in non-small-cell lung cancer Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Response to irinotecan and platinum-based chemotherapy in non-small-cell lung cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
non-small cell lung carcinoma Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease non-small cell lung carcinoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
small intestine neoplasm Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease small intestine neoplasm in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
lung small cell carcinoma Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease lung small cell carcinoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
abnormality of the small intestine Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the small intestine phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
small intestine Gene SetFrom HPA Tissue Gene Expression Profiles genes with high or low expression in small intestine relative to other tissues from the HPA Tissue Gene Expression Profiles dataset. |
small intestine Gene SetFrom HPA Tissue Protein Expression Profiles proteins with high or low expression in small intestine relative to other tissues from the HPA Tissue Protein Expression Profiles dataset. |
small cerebral cortex Gene SetFrom HPO Gene-Disease Associations genes associated with the small cerebral cortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small nail Gene SetFrom HPO Gene-Disease Associations genes associated with the small nail phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small pituitary gland Gene SetFrom HPO Gene-Disease Associations genes associated with the small pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small proximal tibial epiphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the small proximal tibial epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small sella turcica Gene SetFrom HPO Gene-Disease Associations genes associated with the small sella turcica phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypotrophy of the small hand muscles Gene SetFrom HPO Gene-Disease Associations genes associated with the hypotrophy of the small hand muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
neoplasm of the small intestine Gene SetFrom HPO Gene-Disease Associations genes associated with the neoplasm of the small intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small foramen magnum Gene SetFrom HPO Gene-Disease Associations genes associated with the small foramen magnum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small anterior fontanelle Gene SetFrom HPO Gene-Disease Associations genes associated with the small anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small epiphyses Gene SetFrom HPO Gene-Disease Associations genes associated with the small epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
decreased number of small peripheral myelinated nerve fibers Gene SetFrom HPO Gene-Disease Associations genes associated with the decreased number of small peripheral myelinated nerve fibers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
arteriosclerosis of small cerebral arteries Gene SetFrom HPO Gene-Disease Associations genes associated with the arteriosclerosis of small cerebral arteries phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small, conical teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the small, conical teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small earlobe Gene SetFrom HPO Gene-Disease Associations genes associated with the small earlobe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small forehead Gene SetFrom HPO Gene-Disease Associations genes associated with the small forehead phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple small vertebral fractures Gene SetFrom 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. |
small cervical vertebral bodies Gene SetFrom 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 intestine carcinoid Gene SetFrom HPO Gene-Disease Associations genes associated with the small intestine carcinoid phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small intestinal polyposis Gene SetFrom HPO Gene-Disease Associations genes associated with the small intestinal polyposis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small hypothenar eminence Gene SetFrom HPO Gene-Disease Associations genes associated with the small hypothenar eminence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of small intestinal villus morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of small intestinal villus morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small vessel vasculitis Gene SetFrom HPO Gene-Disease Associations genes associated with the small vessel vasculitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small intestinal stenosis Gene SetFrom HPO Gene-Disease Associations genes associated with the small intestinal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small thenar eminence Gene SetFrom HPO Gene-Disease Associations genes associated with the small thenar eminence phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small placenta Gene SetFrom HPO Gene-Disease Associations genes associated with the small placenta phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
ankylosis of feet small joints Gene SetFrom HPO Gene-Disease Associations genes associated with the ankylosis of feet small joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small hand Gene SetFrom HPO Gene-Disease Associations genes associated with the small hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the small intestine Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the small intestine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
multiple small medullary renal cysts Gene SetFrom 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. |
brain very small Gene SetFrom HPO Gene-Disease Associations genes associated with the brain very small phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small face Gene SetFrom HPO Gene-Disease Associations genes associated with the small face phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small for gestational age Gene SetFrom HPO Gene-Disease Associations genes associated with the small for gestational age phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
calcification of the small brain vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the calcification of the small brain vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
small abnormally formed scapulae Gene SetFrom HPO Gene-Disease Associations genes associated with the small abnormally formed scapulae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Carcinoma, Small Cell Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Carcinoma, Small Cell phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Carcinoma, Non-Small-Cell Lung Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Carcinoma, Non-Small-Cell Lung phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Small Cell Lung Carcinoma Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Small Cell Lung Carcinoma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Desmoplastic Small Round Cell Tumor Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Desmoplastic Small Round Cell Tumor phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Large neutral amino acids transporter small subunit 4 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Large neutral amino acids transporter small subunit 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small-subunit processome, Utp21 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small-subunit processome, Utp21 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
GyrI-like small molecule binding domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the GyrI-like small molecule binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U2 auxiliary factor small subunit Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U2 auxiliary factor small subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small proline-rich protein/late cornified envelope protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small proline-rich protein/late cornified envelope protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily, Ras type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, Ras type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U3 small nucleolar ribonucleoprotein complex, subunit Mpp10 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U3 small nucleolar ribonucleoprotein complex, subunit Mpp10 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily, Rho type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, Rho type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U1 small nuclear ribonucleoprotein of 70kDa N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U1 small nuclear ribonucleoprotein of 70kDa N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U6 snRNA-associated Sm-like protein LSm4/Small nuclear ribonucleoprotein Sm D1/D3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U6 snRNA-associated Sm-like protein LSm4/Small nuclear ribonucleoprotein Sm D1/D3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily, mitochondrial Rho Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, mitochondrial Rho protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTP-binding protein domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTP-binding protein domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U4/U6 small nuclear ribonucleoprotein Prp31 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U4/U6 small nuclear ribonucleoprotein Prp31 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small nuclear RNA activating complex subunit 2-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small nuclear RNA activating complex subunit 2-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small acidic protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small acidic protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U1 small nuclear ribonucleoprotein C Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U1 small nuclear ribonucleoprotein C protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Clathrin adaptor complex, small chain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Clathrin adaptor complex, small chain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small nuclear RNA activating complex (SNAPc), subunit SNAP43 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small nuclear RNA activating complex (SNAPc), subunit SNAP43 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U3 small nucleolar RNA-associated protein 10 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U3 small nucleolar RNA-associated protein 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribosomal RNA small subunit methyltransferase H Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribosomal RNA small subunit methyltransferase H protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small membrane A-kinase anchor protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small membrane A-kinase anchor protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small nuclear ribonucleoprotein Sm D2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small nuclear ribonucleoprotein Sm D2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily, GEM/REM/Rad Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, GEM/REM/Rad protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA polymerase delta/II small subunit family Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA polymerase delta/II small subunit family protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U3 small nucleolar RNA-associated protein 6 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U3 small nucleolar RNA-associated protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small proline-rich protein 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small proline-rich protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small-subunit processome, Utp13 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small-subunit processome, Utp13 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small-subunit processome, Utp12 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small-subunit processome, Utp12 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small-subunit processome, Utp11 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small-subunit processome, Utp11 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small-subunit processome, Utp14 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small-subunit processome, Utp14 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Carbamoyl-phosphate synthase, small subunit N-terminal domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Carbamoyl-phosphate synthase, small subunit N-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small ribonucleoprotein associated, SmB/SmN Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small ribonucleoprotein associated, SmB/SmN protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Ribonucleotide reductase small subunit Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Ribonucleotide reductase small subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Methyltransferase small domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Methyltransferase small domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small nuclear ribonucleoprotein E Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small nuclear ribonucleoprotein E protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Iron hydrogenase, small subunit-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Iron hydrogenase, small subunit-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U3 small nucleolar RNA-associated protein 15, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U3 small nucleolar RNA-associated protein 15, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Xanthine dehydrogenase, small subunit Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Xanthine dehydrogenase, small subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U4/U6 small nuclear ribonucleoprotein Prp4 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U4/U6 small nuclear ribonucleoprotein Prp4 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
U4/U6 small nuclear ribonucleoprotein Prp3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the U4/U6 small nuclear ribonucleoprotein Prp3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, CybS Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Succinate dehydrogenase [ubiquinone] cytochrome b small subunit, CybS protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Aconitase A/isopropylmalate dehydratase small subunit, swivel Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Aconitase A/isopropylmalate dehydratase small subunit, swivel protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small integral membrane protein 15 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small integral membrane protein 15 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Citrate synthase-like, small alpha subdomain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Citrate synthase-like, small alpha subdomain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small leucine-rich proteoglycan, class I, decorin/asporin/byglycan Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small leucine-rich proteoglycan, class I, decorin/asporin/byglycan protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small ubiquitin-related modifier, chordates Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small ubiquitin-related modifier, chordates protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small subunit of serine palmitoyltransferase-like Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small subunit of serine palmitoyltransferase-like protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small integral membrane protein 19 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small integral membrane protein 19 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small integral membrane protein 10 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small integral membrane protein 10 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA primase, small subunit, eukaryotic/archaeal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA primase, small subunit, eukaryotic/archaeal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily, ARF type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, ARF type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small muscular protein Chisel Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small muscular protein Chisel protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily, SAR1-type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, SAR1-type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small acidic protein-like domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small acidic protein-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily, ARF/SAR type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, ARF/SAR type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DNA primase, small subunit Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DNA primase, small subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Calpain small subunit 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Calpain small subunit 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Small GTPase superfamily, Rab type Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Small GTPase superfamily, Rab type protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Carbamoyl-phosphate synthase, small subunit Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Carbamoyl-phosphate synthase, small subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Sirtuin family, catalytic core small domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Sirtuin family, catalytic core small domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
non small cell lung cancer Gene SetFrom KEGG Pathways proteins participating in the non small cell lung cancer pathway from the KEGG Pathways dataset. |
small cell lung cancer Gene SetFrom KEGG Pathways proteins participating in the small cell lung cancer pathway from the KEGG Pathways dataset. |
small endolymphatic duct Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small endolymphatic duct phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small sebaceous gland Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small sebaceous gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small pharynx Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small pharynx phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small vagina Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small vagina phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small nasal bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small nasal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small alisphenoid bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small alisphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small trigeminal motor nucleus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small trigeminal motor nucleus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small pituitary gland Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small pituitary gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small alveolar lamellar bodies Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small alveolar lamellar bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small basioccipital bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small basioccipital bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small floor plate Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small floor plate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small epididymis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small epididymis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased small intestinal microvillus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased small intestinal microvillus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal small intestine crypts of lieberkuhn morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal small intestine crypts of lieberkuhn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small premaxilla Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small premaxilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small superior glossopharyngeal ganglion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small superior glossopharyngeal ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small proamniotic cavity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small proamniotic cavity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small gallbladder Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small gallbladder phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small cochlear ganglion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small cochlear ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small malleus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small malleus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small esophagus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small esophagus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small otic capsule Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small otic capsule phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small lymph nodes Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small lymph nodes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small ischium Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small ischium phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small molars Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small molars phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small cecum Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small cecum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small seminal vesicle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small seminal vesicle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small sacral vertebrae Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small sacral vertebrae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small penile bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small penile bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small spleen Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small spleen phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased small intestinal villus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased small intestinal villus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small olfactory bulb Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small olfactory bulb phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small inner medullary pyramid Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small inner medullary pyramid phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small male preputial glands Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small male preputial glands phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small geniculate ganglion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small geniculate ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small popliteal lymph nodes Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small popliteal lymph nodes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small visceral yolk sac Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small visceral yolk sac phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased small intestine adenocarcinoma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased small intestine adenocarcinoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small pterygoid bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small pterygoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal small intestinal crypt cell proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal small intestinal crypt cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small second pharyngeal arch Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small second pharyngeal arch phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small lung saccule Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small lung saccule phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small ears Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small ears phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small caput epididymis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small caput epididymis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small caudal vertebrae Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small caudal vertebrae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small submandibular ganglion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small submandibular ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small trachea Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small trachea phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small exoccipital bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small exoccipital bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small limb buds Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small limb buds phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small myocardial fiber Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small myocardial fiber phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased lung non-small cell carcinoma incidence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased lung non-small cell carcinoma incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small l5 dorsal root ganglion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small l5 dorsal root ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small clavicle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small clavicle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small uterus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small uterus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small vestibular ganglion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small vestibular ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal small intestine placement Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal small intestine placement phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small petrosal ganglion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small petrosal ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small superior cervical ganglion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small superior cervical ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small ectoplacental cone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small ectoplacental cone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small vulva Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small vulva phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small pancreatic islets Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small pancreatic islets phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small thyroid gland Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small thyroid gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small lymphoid organs Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small lymphoid organs phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small interparietal bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small interparietal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small prostate gland ventral lobe Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small prostate gland ventral lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small peyer's patches Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small peyer's patches phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small scrotum Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small scrotum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small vertebrae Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small vertebrae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small ureteric bud Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small ureteric bud phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small seminiferous tubules Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small seminiferous tubules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small maxilla Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small maxilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small testis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small testis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small perianal sebaceous gland Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small perianal sebaceous gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small basisphenoid bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small basisphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small pancreas Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small pancreas phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small lens Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small lens phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small inguinal lymph nodes Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small inguinal lymph nodes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small endometrial glands Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small endometrial glands phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small pubis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small pubis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small thymus Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small thymus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small pituitary intermediate lobe Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small pituitary intermediate lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small parietal bone Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small parietal bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small adenohypophysis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small adenohypophysis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small kidney Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small kidney phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small xiphoid process Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small xiphoid process phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |