Name

MCOPCT1 Gene

cataract, congenital, with microphthalmia

CFTDX Gene

Myopathy, congenital, with fiber-type disproportion, X-linked

NPHS1 Gene

nephrosis 1, congenital, Finnish type (nephrin)

This gene encodes a member of the immunoglobulin family of cell adhesion molecules that functions in the glomerular filtration barrier in the kidney. The gene is primarily expressed in renal tissues, and the protein is a type-1 transmembrane protein found at the slit diaphragm of glomerular podocytes. The slit diaphragm is thought to function as an ultrafilter to exclude albumin and other plasma macromolecules in the formation of urine. Mutations in this gene result in Finnish-type congenital nephrosis 1, characterized by severe proteinuria and loss of the slit diaphragm and foot processes.[provided by RefSeq, Oct 2009]

CTRCT37 Gene

Cataract, congenital cerulean type, 5

CTRCT34 Gene

Cataract, autosomal recessive congenital 3

CTRCT35 Gene

cataract, congenital nuclear, autosomal recessive

BSCL2 Gene

Berardinelli-Seip congenital lipodystrophy 2 (seipin)

This gene encodes the multi-pass transmembrane protein seipin. This protein localizes to the endoplasmic reticulum and may be important for lipid droplet morphology. Mutations in this gene have been associated with congenital generalized lipodystrophy type 2 or Berardinelli-Seip syndrome, a rare autosomal recessive disease characterized by a near absence of adipose tissue and severe insulin resistance. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. Naturally occurring read-through transcription occurs between this locus and the neighboring locus HNRNPUL2 (heterogeneous nuclear ribonucleoprotein U-like 2).[provided by RefSeq, Jul 2024]

HTC1 Gene

hypertrichosis 1 (universalis, congenital)

HTC2 Gene

hypertrichosis 2 (generalized, congenital)

RNANC Gene

Retinal nonattachment, nonsyndromic congenital

NHS Gene

Nance-Horan syndrome (congenital cataracts and dental anomalies)

This gene encodes a protein containing four conserved nuclear localization signals. The encoded protein functions in eye, tooth, craniofacial and brain development, and it can regulate actin remodeling and cell morphology. Mutations in this gene have been shown to cause Nance-Horan syndrome, and also X-linked cataract-40. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, May 2014]

MDC1B Gene

Muscular dystrophy, congenital, 1B

CDAN3 Gene

congenital dyserythropoietic anemia, type III

LCA5L Gene

Leber congenital amaurosis 5-like

Predicted to be involved in intraciliary transport. Predicted to be active in axoneme. [provided by Alliance of Genome Resources, Mar 2025]

NDNC9 Gene

Nail disorder, nonsyndromic congenital, 9

NYS2 Gene

nystagmus 2, congenital autosomal dominant

NYS3 Gene

nystagmus 3, congenital autosomal dominant

NYS7 Gene

Nystagmus 7, congenital

NYS4 Gene

nystagmus 4, congenital autosomal dominant

NDIC Gene

Nail dysplasia, isolated congenital

CTRCT27 Gene

Cataract, congenital, nuclear progressive

PTOS2 Gene

Ptosis, hereditary congenital 2

PTOS1 Gene

ptosis, congenital 1 (autosomal dominant)

GLC3C Gene

glaucoma 3, primary congenital, C

SMAL Gene

spinal muscular atrophy, congenital nonprogressive, of lower limbs

ANIC Gene

Anosmia, isolated congenital

CHDT3 Gene

Congenital heart defects, multiple types, 3

MDCMP Gene

muscular dystrophy, congenital, merosin-positive

CHNG3 Gene

Hypothyroidism, congenital, nongoitrous, 3

LCA5 Gene

Leber congenital amaurosis 5

This gene encodes a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Alternatively spliced transcript variants are described. [provided by RefSeq, Oct 2009]

CCA1 Gene

cataract, congenital, cerulean type, 1

CCT Gene

cataract, congenital, total

CCV Gene

cataract, congenital, Volkmann type

MCOR Gene

microcoria, congenital

DIH2 Gene

Hernia, congenital diaphragmatic 2

ARCI9 Gene

Ichthyosis, congenital, autosomal recessive 9

ARCI7 Gene

Ichthyosis, congenital, autosomal recessive 7

PAFC Gene

Preauricular fistulae, congenital

GJC2 Gene

gap junction protein, gamma 2, 47kDa

This gene encodes a gap junction protein. Gap junction proteins are members of a large family of homologous connexins and comprise 4 transmembrane, 2 extracellular, and 3 cytoplasmic domains. This gene plays a key role in central myelination and is involved in peripheral myelination in humans. Defects in this gene are the cause of autosomal recessive Pelizaeus-Merzbacher-like disease-1. [provided by RefSeq, Jul 2008]

GJC3 Gene

gap junction protein, gamma 3, 30.2kDa

This gene encodes a gap junction protein. The encoded protein, also known as a connexin, plays a role in formation of gap junctions, which provide direct connections between neighboring cells. Mutations in this gene have been reported to be associated with nonsyndromic hearing loss.[provided by RefSeq, Feb 2010]

GJC1 Gene

gap junction protein, gamma 1, 45kDa

This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Alternatively spliced transcript variants encoding the same isoform have been described. [provided by RefSeq, Jul 2008]

GJB6 Gene

gap junction protein, beta 6, 30kDa

Gap junctions allow the transport of ions and metabolites between the cytoplasm of adjacent cells. They are formed by two hemichannels, made up of six connexin proteins assembled in groups. Each connexin protein has four transmembrane segments, two extracellular loops, a cytoplasmic loop formed between the two inner transmembrane segments, and the N- and C-terminus both being in the cytoplasm. The specificity of the gap junction is determined by which connexin proteins comprise the hemichannel. In the past, connexin protein names were based on their molecular weight, however the new nomenclature uses sequential numbers based on which form (alpha or beta) of the gap junction is present. This gene encodes one of the connexin proteins. Mutations in this gene have been found in some forms of deafness and in some families with hidrotic ectodermal dysplasia. [provided by RefSeq, Jul 2008]

GJE1 Gene

gap junction protein, epsilon 1, 23kDa

Predicted to enable gap junction channel activity. Predicted to be involved in cell-cell signaling. Predicted to act upstream of or within cell morphogenesis; lens development in camera-type eye; and organ growth. Predicted to be located in plasma membrane. Predicted to be part of connexin complex. [provided by Alliance of Genome Resources, Mar 2025]

PUJO Gene

pelviureteric junction obstruction

JUP Gene

junction plakoglobin

This gene encodes a major cytoplasmic protein which is the only known constituent common to submembranous plaques of both desmosomes and intermediate junctions. This protein forms distinct complexes with cadherins and desmosomal cadherins and is a member of the catenin family since it contains a distinct repeating amino acid motif called the armadillo repeat. Mutation in this gene has been associated with Naxos disease. Alternative splicing occurs in this gene; however, not all transcripts have been fully described. [provided by RefSeq, Jul 2008]

TJAP1 Gene

tight junction associated protein 1 (peripheral)

This gene encodes a tight junction-associated protein. Incorporation of the encoded protein into tight junctions occurs at a late stage of formation of the junctions. The encoded protein localizes to the Golgi and may function in vesicle trafficking. Alternatively spliced transcript variants have been described. A related pseudogene exists on the X chromosome. [provided by RefSeq, Mar 2009]

JMY Gene

junction mediating and regulatory protein, p53 cofactor

Enables microtubule binding activity. Involved in cellular response to starvation. Located in autophagosome membrane; cell leading edge; and cytoplasmic vesicle. [provided by Alliance of Genome Resources, Mar 2025]

LOC126987 Gene

tight junction protein 3 (zona occludens 3) pseudogene

GEN1 Gene

GEN1 Holliday junction 5' flap endonuclease

This gene encodes a member of the Rad2/xeroderma pigmentosum group G nuclease family, whose members are characterized by N-terminal and internal xeroderma pigmentosum group G nuclease domains followed by helix-hairpin-helix domains and disordered C-terminal domains. The protein encoded by this gene is involved in resolution of Holliday junctions, which are intermediate four-way structures that covalently link DNA during homologous recombination and double-strand break repair. The protein resolves Holliday junctions by creating dual incisions across the junction to produce nicked duplex products that can be ligated. In addition, this protein has been found to localize to centrosomes where it has been implicated in regulation of centrosome integrity. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2016]

GJB7 Gene

gap junction protein, beta 7, 25kDa

Connexins, such as GJB7, are involved in the formation of gap junctions, intercellular conduits that directly connect the cytoplasms of contacting cells. Each gap junction channel is formed by docking of 2 hemichannels, each of which contains 6 connexin subunits (Sohl et al., 2003 [PubMed 12881038]).[supplied by OMIM, Mar 2008]

GJA1P1 Gene

gap junction protein, alpha 1, 43kDa pseudogene 1

LOC100128334 Gene

gap junction protein, gamma 3, 30.2kDa pseudogene

TJP2 Gene

tight junction protein 2

This gene encodes a zonula occluden that is a member of the membrane-associated guanylate kinase homolog family. The encoded protein functions as a component of the tight junction barrier in epithelial and endothelial cells and is necessary for proper assembly of tight junctions. Mutations in this gene have been identified in patients with hypercholanemia, and genomic duplication of a 270 kb region including this gene causes autosomal dominant deafness-51. Alternatively spliced transcripts encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]

TJP3 Gene

tight junction protein 3

The protein encoded by this gene is a member of the membrane-associated guanylate kinase-like (MAGUK) protein family which is characterized by members having multiple PDZ domains, a single SH3 domain, and a single guanylate kinase-like (GUK)-domain. In addition, members of the zonula occludens protein subfamily have an acidic domain, a basic arginine-rich region, and a proline-rich domain. The protein encoded by this gene plays a role in the linkage between the actin cytoskeleton and tight-junctions and also sequesters cyclin D1 at tight junctions during mitosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms. This gene has a partial pseudogene on chromosome 1. [provided by RefSeq, May 2012]

TJP1 Gene

tight junction protein 1

This gene encodes a member of the membrane-associated guanylate kinase (MAGUK) family of proteins, and acts as a tight junction adaptor protein that also regulates adherens junctions. Tight junctions regulate the movement of ions and macromolecules between endothelial and epithelial cells. The multidomain structure of this scaffold protein, including a postsynaptic density 95/disc-large/zona occludens (PDZ) domain, a Src homology (SH3) domain, a guanylate kinase (GuK) domain and unique (U) motifs all help to co-ordinate binding of transmembrane proteins, cytosolic proteins, and F-actin, which are required for tight junction function. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Aug 2017]

GJB1 Gene

gap junction protein, beta 1, 32kDa

This gene encodes a member of the gap junction protein family. The gap junction proteins are membrane-spanning proteins that assemble to form gap junction channels that facilitate the transfer of ions and small molecules between cells. According to sequence similarities at the nucleotide and amino acid levels, the gap junction proteins are divided into two categories, alpha and beta. Mutations in this gene cause X-linked Charcot-Marie-Tooth disease, an inherited peripheral neuropathy. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Oct 2008]

GJB3 Gene

gap junction protein, beta 3, 31kDa

This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Mutations in this gene can cause non-syndromic deafness or erythrokeratodermia variabilis, a skin disorder. Alternative splicing results in multiple transcript variants encoding the same protein. [provided by RefSeq, Jul 2008]

GJB2 Gene

gap junction protein, beta 2, 26kDa

This gene encodes a member of the gap junction protein family. The gap junctions were first characterized by electron microscopy as regionally specialized structures on plasma membranes of contacting adherent cells. These structures were shown to consist of cell-to-cell channels that facilitate the transfer of ions and small molecules between cells. The gap junction proteins, also known as connexins, purified from fractions of enriched gap junctions from different tissues differ. According to sequence similarities at the nucleotide and amino acid levels, the gap junction proteins are divided into two categories, alpha and beta. Mutations in this gene are responsible for as much as 50% of pre-lingual, recessive deafness. [provided by RefSeq, Oct 2008]

GJB5 Gene

gap junction protein, beta 5, 31.1kDa

This gene encodes a member of the beta-type (group I) connexin family. The encoded protein is a gap junction protein involved in intercellular communication related to epidermal differentiation and environmental sensing. This gene has been linked to non-small cell lung cancer. [provided by RefSeq, Nov 2012]

GJB4 Gene

gap junction protein, beta 4, 30.3kDa

This gene encodes a transmembrane connexin protein that is a component of gap junctions. Mutations in this gene have been associated with erythrokeratodermia variabilis, progressive symmetric erythrokeratoderma and hearing impairment. [provided by RefSeq, Dec 2009]

GJA10 Gene

gap junction protein, alpha 10, 62kDa

Connexins, such as GJA10, are involved in the formation of gap junctions, intercellular conduits that directly connect the cytoplasms of contacting cells. Each gap junction channel is formed by docking of 2 hemichannels, each of which contains 6 connexin subunits (Sohl et al., 2003 [PubMed 12881038]).[supplied by OMIM, Mar 2008]

LOC100421028 Gene

gap junction protein, alpha 4, 37kDa pseudogene

GJA1 Gene

gap junction protein, alpha 1, 43kDa

This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. The encoded protein is the major protein of gap junctions in the heart that are thought to have a crucial role in the synchronized contraction of the heart and in embryonic development. A related intronless pseudogene has been mapped to chromosome 5. Mutations in this gene have been associated with oculodentodigital dysplasia, autosomal recessive craniometaphyseal dysplasia and heart malformations. [provided by RefSeq, May 2014]

GJA3 Gene

gap junction protein, alpha 3, 46kDa

The protein encoded by this gene is a connexin and is a component of lens fiber gap junctions. Defects in this gene are a cause of zonular pulverulent cataract type 3 (CZP3). [provided by RefSeq, Jan 2010]

GJA4 Gene

gap junction protein, alpha 4, 37kDa

This gene encodes a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Mutations in this gene have been associated with atherosclerosis and a higher risk of myocardial infarction. [provided by RefSeq, Jul 2008]

GJA5 Gene

gap junction protein, alpha 5, 40kDa

This gene is a member of the connexin gene family. The encoded protein is a component of gap junctions, which are composed of arrays of intercellular channels that provide a route for the diffusion of low molecular weight materials from cell to cell. Mutations in this gene may be associated with atrial fibrillation. Alternatively spliced transcript variants encoding the same isoform have been described. [provided by RefSeq, Jul 2008]

GJA8 Gene

gap junction protein, alpha 8, 50kDa

This gene encodes a transmembrane connexin protein that is necessary for lens growth and maturation of lens fiber cells. The encoded protein is a component of gap junction channels and functions in a calcium and pH-dependent manner. Mutations in this gene have been associated with zonular pulverulent cataracts, nuclear progressive cataracts, and cataract-microcornea syndrome. [provided by RefSeq, Dec 2009]

GJA9 Gene

gap junction protein, alpha 9, 59kDa

Connexins, such as GJA9, are involved in the formation of gap junctions, intercellular conduits that directly connect the cytoplasms of contacting cells. Each gap junction channel is formed by docking of 2 hemichannels, each of which contains 6 connexin subunits (Sohl et al., 2003 [PubMed 12881038]).[supplied by OMIM, Mar 2008]

GJA6P Gene

gap junction protein, alpha 6, pseudogene

LOC392539 Gene

tight junction associated protein 1 pseudogene

GJD4 Gene

gap junction protein, delta 4, 40.1kDa

Connexins, such as GJD4, are involved in the formation of gap junctions, intercellular conduits that directly connect the cytoplasms of contacting cells. Each gap junction channel is formed by docking of 2 hemichannels, each of which contains 6 connexin subunits (Sohl et al., 2003 [PubMed 12881038]).[supplied by OMIM, Mar 2008]

GJD3 Gene

gap junction protein, delta 3, 31.9kDa

This gene is a member of the large family of connexins that are required for the formation of gap junctions. Six connexin monomers form a hemichannel, or connexon, on the cell surface. This connexon can interact with a connexon from a neighboring cell, thus forming a channel linking the cytoplasm of the 2 cells. [provided by RefSeq, Jul 2008]

GJD2 Gene

gap junction protein, delta 2, 36kDa

This gene encodes a member of the connexin protein family. Connexins are gap junction proteins which are arranged in groups of 6 around a central pore to form a connexon, a component of the gap junction intercellular channel. The channels formed by this protein allow cationic molecule exchange between human beta cells and may function in the regulation of insulin secretion. [provided by RefSeq, Oct 2012]

TJP1P Gene

tight junction protein 1 pseudogene

HJURP Gene

Holliday junction recognition protein

Enables histone binding activity and identical protein binding activity. Involved in CENP-A containing chromatin assembly; chromosome segregation; and regulation of protein-containing complex assembly. Located in cytosol; kinetochore; and nuclear lumen. [provided by Alliance of Genome Resources, Mar 2025]

PYM1 Gene

PYM homolog 1, exon junction complex associated factor

Enables ribosome binding activity. Involved in exon-exon junction complex disassembly; nuclear-transcribed mRNA catabolic process, nonsense-mediated decay; and positive regulation of translation. Located in cell junction; cytosol; and nuclear lumen. Part of exon-exon junction complex. [provided by Alliance of Genome Resources, Mar 2025]

LNPK Gene

lunapark, ER junction formation factor

Enables identical protein binding activity. Involved in endoplasmic reticulum tubular network maintenance and positive regulation of endoplasmic reticulum tubular network organization. Located in endoplasmic reticulum tubular network membrane and nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025]

AFDN Gene

afadin, adherens junction formation factor

This gene encodes a multi-domain protein involved in signaling and organization of cell junctions during embryogenesis. It has also been identified as the fusion partner of acute lymphoblastic leukemia (ALL-1) gene, involved in acute myeloid leukemias with t(6;11)(q27;q23) translocation. Alternatively spliced transcript variants encoding different isoforms have been described for this gene, however, not all have been fully characterized.[provided by RefSeq, May 2011]

AJM1 Gene

apical junction component 1 homolog

Predicted to be involved in cell-cell junction organization. Predicted to be located in adherens junction; apical plasma membrane; and cilium. Predicted to be active in apical junction complex and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025]

JAML Gene

junction adhesion molecule like

Enables integrin binding activity and protein homodimerization activity. Involved in heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules and myeloid leukocyte migration. Located in bicellular tight junction; nucleoplasm; and plasma membrane. [provided by Alliance of Genome Resources, Mar 2025]

MAJIN Gene

membrane anchored junction protein

Predicted to enable DNA binding activity. Predicted to be involved in homologous chromosome pairing at meiosis and meiotic attachment of telomere to nuclear envelope. Predicted to act upstream of or within double-strand break repair involved in meiotic recombination; oogenesis; and spermatogenesis. Predicted to be located in chromosome, telomeric region. Predicted to be active in nuclear inner membrane. [provided by Alliance of Genome Resources, Mar 2025]

Congenital Ureteropelvic Junction Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Ureteropelvic Junction Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

ureteropelvic junction obstruction Gene Set

From HPO Gene-Disease Associations

genes associated with the ureteropelvic junction obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ureteropelvic junction obstruction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ureteropelvic junction obstruction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ureteropelvic junction obstruction Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the ureteropelvic junction obstruction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Ureteropelvic junction obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Ureteropelvic junction obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

ureteropelvic junction atresia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ureteropelvic junction atresia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ureteropelvic junction stenosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ureteropelvic junction stenosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ureteropelvic junction morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ureteropelvic junction morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ureteropelvic junction morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal ureteropelvic junction morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

ureteropelvic junction atresia Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the ureteropelvic junction atresia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

ureteropelvic junction stenosis Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the ureteropelvic junction stenosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Congenital Pelviureteric Junction Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Pelviureteric Junction Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; ventricular outflow obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; ventricular outflow obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ureterovesical junction obstruction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ureterovesical junction obstruction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

pelviureteric junction obstruction Gene Set

From OMIM Gene-Disease Associations

genes associated with the pelviureteric junction obstruction phenotype from the curated OMIM Gene-Disease Associations dataset.

Ureterovesical Junction Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ureterovesical Junction Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Obstruction Of Pelviureteric Junction Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Obstruction Of Pelviureteric Junction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

ureterovesical junction obstruction Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the ureterovesical junction obstruction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

ureteropelvic Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ureteropelvic in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Congenital Obstruction Of Bladder Neck Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Obstruction Of Bladder Neck in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Urinary Tract Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Urinary Tract Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Duodenal Obstruction Due To Malrotation Of Intestine Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Duodenal Obstruction Due To Malrotation Of Intestine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Congenital Intestinal Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Congenital Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Familial congenital nasolacrimal duct obstruction Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Familial congenital nasolacrimal duct obstruction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Airway Obstruction Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Airway Obstruction from the curated CTD Gene-Disease Associations dataset.

Nasal Obstruction Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nasal Obstruction from the curated CTD Gene-Disease Associations dataset.

Renal Artery Obstruction Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal Artery Obstruction from the curated CTD Gene-Disease Associations dataset.

Intestinal Obstruction Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Intestinal Obstruction from the curated CTD Gene-Disease Associations dataset.

Ventricular Outflow Obstruction Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ventricular Outflow Obstruction from the curated CTD Gene-Disease Associations dataset.

Urinary Bladder Neck Obstruction Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Urinary Bladder Neck Obstruction from the curated CTD Gene-Disease Associations dataset.

Ureteral Obstruction Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ureteral Obstruction from the curated CTD Gene-Disease Associations dataset.

intestinal pseudo-obstruction Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease intestinal pseudo-obstruction from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

intestinal obstruction Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease intestinal obstruction from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

gastric outlet obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease gastric outlet obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

urinary tract obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease urinary tract obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

lacrimal duct obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease lacrimal duct obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

colonic pseudo-obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease colonic pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease intestinal obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

ureteral obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease ureteral obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

bladder neck obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease bladder neck obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

urethral obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease urethral obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

renal artery obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease renal artery obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

intestinal pseudo-obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease intestinal pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

duodenal obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease duodenal obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

atherosclerosis; hypertension, renovascular; renal artery obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atherosclerosis; hypertension, renovascular; renal artery obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intestinal pseudo-obstruction; mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intestinal pseudo-obstruction; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

airway obstruction; alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease airway obstruction; alpha 1-antitrypsin deficiency; pulmonary disease, chronic obstructive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary artery disease; hypertension; renal artery obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery disease; hypertension; renal artery obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fibromuscular dysplasia; hypertension; renal artery obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fibromuscular dysplasia; hypertension; renal artery obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hay fever; nasal obstruction; rhinitis, allergic, perennial; rhinitis, allergic, seasonal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hay fever; nasal obstruction; rhinitis, allergic, perennial; rhinitis, allergic, seasonal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

late-onset airflow obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease late-onset airflow obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; intestinal obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease constriction, pathologic; crohn disease; crohn's disease; intestinal fistula; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

deafness; diabetes complications; diabetes mellitus; intestinal pseudo-obstruction; pancreatitis; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease deafness; diabetes complications; diabetes mellitus; intestinal pseudo-obstruction; pancreatitis; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

crohn disease; crohn's disease; intestinal obstruction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease crohn disease; crohn's disease; intestinal obstruction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

airway obstruction; asthma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease airway obstruction; asthma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obstruction Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term obstruction in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Airflow obstruction Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Airflow obstruction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

gastric outlet obstruction Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease gastric outlet obstruction in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

urethral obstruction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the urethral obstruction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

gastrointestinal obstruction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the gastrointestinal obstruction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

intestinal obstruction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the intestinal obstruction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

intestinal obstruction Gene Set

From HPO Gene-Disease Associations

genes associated with the intestinal obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intestinal pseudo-obstruction Gene Set

From HPO Gene-Disease Associations

genes associated with the intestinal pseudo-obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

gastrointestinal obstruction Gene Set

From HPO Gene-Disease Associations

genes associated with the gastrointestinal obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

episodic upper airway obstruction Gene Set

From HPO Gene-Disease Associations

genes associated with the episodic upper airway obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

right ventricular outlet obstruction Gene Set

From HPO Gene-Disease Associations

genes associated with the right ventricular outlet obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

nasal obstruction Gene Set

From HPO Gene-Disease Associations

genes associated with the nasal obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

nasolacrimal duct obstruction Gene Set

From HPO Gene-Disease Associations

genes associated with the nasolacrimal duct obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

upper airway obstruction Gene Set

From HPO Gene-Disease Associations

genes associated with the upper airway obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ureteral obstruction Gene Set

From HPO Gene-Disease Associations

genes associated with the ureteral obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

urethral obstruction Gene Set

From HPO Gene-Disease Associations

genes associated with the urethral obstruction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Airway Obstruction Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Airway Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Nasal Obstruction Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Nasal Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Renal Artery Obstruction Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Renal Artery Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Intestinal Obstruction Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Intestinal Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ventricular Outflow Obstruction Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ventricular Outflow Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Gastric Outlet Obstruction Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Gastric Outlet Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Intestinal Pseudo-Obstruction Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Intestinal Pseudo-Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ureteral Obstruction Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ureteral Obstruction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

urinary bladder obstruction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the urinary bladder obstruction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

intestinal obstruction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the intestinal obstruction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

rete testis obstruction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the rete testis obstruction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ureter obstruction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ureter obstruction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

urethra obstruction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the urethra obstruction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Obstruction Of Biliary Tree Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Obstruction Of Biliary Tree in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Urinary Tract Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Urinary Tract Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Chronic Intestinal Pseudo-Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Chronic Intestinal Pseudo-Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Pseudo-Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Pseudo-Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Bladder Neck Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Bladder Neck Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Prostatic Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Prostatic Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Urinary Outflow Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Urinary Outflow Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Unilateral Nasal Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Unilateral Nasal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Upper Airway Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Upper Airway Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Urethral Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Urethral Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Bronchial Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Bronchial Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Chronic Airflow Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Chronic Airflow Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Left Ventricular Outflow Tract Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Left Ventricular Outflow Tract Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Distal Ileal Obstruction Syndrome Gene Set

From 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 Set

From 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.

Urethral Obstruction Sequence Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Urethral Obstruction Sequence in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Obstruction Of Colon Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Obstruction Of Colon in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Intestinal Obstruction Co-Occurrent And Due To Decreased Peristalsis Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Intestinal Obstruction Co-Occurrent And Due To Decreased Peristalsis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Neonatal Intestinal Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Neonatal Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Portal Vein Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Portal Vein Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Acute Intestinal Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Acute Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Malignant Biliary Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Malignant Biliary Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lacrimal Duct Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lacrimal Duct Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Lower Airway Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Lower Airway Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Ventricular Outflow Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Ventricular Outflow Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Bladder Outflow Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Bladder Outflow Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Small Bowel Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Small Bowel Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Bilateral Nasal Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Bilateral Nasal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Primary Acquired Nasolacrimal Duct Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Primary Acquired Nasolacrimal Duct Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Renal Artery Obstruction Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Renal Artery Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Other Ureteric Obstruction Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Other Ureteric Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Ureteral Obstruction Gene Set

From DisGeNET Gene-Phenotype Associations

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

Nasal Obstruction Present Finding Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Nasal Obstruction Present Finding in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Functional Intestinal Obstruction Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Functional Intestinal Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Laryngeal Obstruction Gene Set

From DisGeNET Gene-Phenotype Associations

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

Malignant Bowel Obstruction Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Malignant Bowel Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Obstruction Of Nasolacrimal Duct Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Obstruction Of Nasolacrimal Duct in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Episodic Upper Airway Obstruction Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Episodic Upper Airway Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Ventricular Outflow Obstruction Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Ventricular Outflow Obstruction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Stricture Obstruction Gene Set

From DisGeNET Gene-Phenotype Associations

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

Gastrointestinal Obstruction Gene Set

From DisGeNET Gene-Phenotype Associations

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

Lymphatic Obstruction Gene Set

From DisGeNET Gene-Phenotype Associations

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

intestinal obstruction Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the intestinal obstruction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

rete testis obstruction Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the rete testis obstruction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

urinary bladder obstruction Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the urinary bladder obstruction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

urethra obstruction Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the urethra obstruction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

ureter obstruction Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the ureter obstruction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

nasal obstruction Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the nasal obstruction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

urinary bladder obstruction Gene Set

From IMPC Knockout Mouse Phenotypes

gene knockouts causing the urinary bladder obstruction phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.

Intestinal pseudo-obstruction Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Intestinal pseudo-obstruction from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Intestinal obstruction Gene Set

From DISEASES Experimental Gene-Disease Association Evidence Scores 2025

genes associated with the disease Intestinal obstruction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.

Gastric outlet obstruction Gene Set

From DISEASES Experimental Gene-Disease Association Evidence Scores 2025

genes associated with the disease Gastric outlet obstruction in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intestinal obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Urinary tract obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Urinary tract obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Ureteral obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Ureteral obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Duodenal obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Duodenal obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Gastric outlet obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Gastric outlet obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal pseudo-obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Intestinal pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Colonic pseudo-obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Colonic pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Urethral obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Urethral obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Lacrimal duct obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Lacrimal duct obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Bladder neck obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Bladder neck obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Renal artery obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Renal artery obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

X-linked chronic idiopathic intestinal pseudo-obstruction Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease X-linked chronic idiopathic intestinal pseudo-obstruction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Intestinal pseudo-obstruction Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Intestinal pseudo-obstruction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Intestinal obstruction Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Intestinal obstruction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Lower urinary tract obstruction Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Lower urinary tract obstruction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Airflow obstruction in ever smokers Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Airflow obstruction in ever smokers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Airway obstruction (FEV1/FVC<70%) in never smokers Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Airway obstruction (FEV1/FVC<70%) in never smokers phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Airway obstruction (FEV1/FVC Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Airway obstruction (FEV1/FVC

Airflow obstruction Gene Set

From GWAS Catalog SNP-Phenotype Associations 2025

genes associated with the Airflow obstruction phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

congenital heart defects; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; folic acid deficiency; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; folic acid deficiency; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal hyperplasia, congenital; congenital adrenal hyperplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; congenital heart defects; growth disorders; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; down syndrome; heart defects, congenital; heart septal defects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; down syndrome; heart defects, congenital; heart septal defects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Heart Defects, Congenital, And Other Congenital Anomalies Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Heart Defects, Congenital, And Other Congenital Anomalies in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

cell junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cell junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

spot adherens junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the spot adherens junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

gap junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the gap junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

tight junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the tight junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cell-substrate junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cell-substrate junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cell-cell junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cell-cell junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

muscle tendon junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the muscle tendon junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

apical junction complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the apical junction complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

occluding junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the occluding junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cell-cell adherens junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cell-cell adherens junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cell-substrate adherens junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cell-substrate adherens junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

exon-exon junction complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the exon-exon junction complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

adherens junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the adherens junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

anchoring junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the anchoring junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

paranodal junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the paranodal junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

neuromuscular junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the neuromuscular junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cell-substrate junction Gene Set

From COMPARTMENTS Experimental Protein Localization Evidence Scores

proteins localized to the cell-substrate junction cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.

adherens junction Gene Set

From COMPARTMENTS Experimental Protein Localization Evidence Scores

proteins localized to the adherens junction cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.

anchoring junction Gene Set

From COMPARTMENTS Experimental Protein Localization Evidence Scores

proteins localized to the anchoring junction cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.

cell junction Gene Set

From COMPARTMENTS Experimental Protein Localization Evidence Scores

proteins localized to the cell junction cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.

cell-substrate adherens junction Gene Set

From COMPARTMENTS Experimental Protein Localization Evidence Scores

proteins localized to the cell-substrate adherens junction cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.

cell junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cell junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

spot adherens junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the spot adherens junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

gap junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the gap junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

tight junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the tight junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

cell-substrate junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cell-substrate junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

septate junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the septate junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

anchoring junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the anchoring junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

nucleus-vacuole junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the nucleus-vacuole junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

cell-cell junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cell-cell junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

smooth septate junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the smooth septate junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

muscle tendon junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the muscle tendon junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

holliday junction resolvase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the holliday junction resolvase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

apical junction complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the apical junction complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

occluding junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the occluding junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

pleated septate junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the pleated septate junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

cell-cell adherens junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cell-cell adherens junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

cell-substrate adherens junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cell-substrate adherens junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

exon-exon junction complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the exon-exon junction complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

mitochondrial crista junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the mitochondrial crista junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

adherens junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the adherens junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

paranodal junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the paranodal junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

neuromuscular junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the neuromuscular junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Exon junction complex (EIF4A3-MLN51-MAGOH-Y14) Gene Set

From CORUM Protein Complexes

proteins in the Exon junction complex (EIF4A3-MLN51-MAGOH-Y14) protein complex from the CORUM Protein Complexes dataset.

Exon junction complex (EIF4A3-MLN51-MAGOH-Y14), RNA-protein complex Gene Set

From CORUM Protein Complexes

proteins in the Exon junction complex (EIF4A3-MLN51-MAGOH-Y14), RNA-protein complex protein complex from the CORUM Protein Complexes dataset.

Exon junction complex (mRNA splicing-dependent) Gene Set

From CORUM Protein Complexes

proteins in the Exon junction complex (mRNA splicing-dependent) protein complex from the CORUM Protein Complexes dataset.

Cell-cell junction complex (ARHGAP10-CTNNA1) Gene Set

From CORUM Protein Complexes

proteins in the Cell-cell junction complex (ARHGAP10-CTNNA1) protein complex from the CORUM Protein Complexes dataset.

Exon junction complex, EIF4A3-MLN51-MAGOH-Y14 (RNA-protein complex) Gene Set

From CORUM Protein Complexes

proteins in the Exon junction complex, EIF4A3-MLN51-MAGOH-Y14 (RNA-protein complex) protein complex from the CORUM Protein Complexes dataset.

Exon junction complex Gene Set

From CORUM Protein Complexes

proteins in the Exon junction complex protein complex from the CORUM Protein Complexes dataset.

Exon junction complex (EIF4A3-MLN51-UPF3B-MAGOH-Y14) Gene Set

From CORUM Protein Complexes

proteins in the Exon junction complex (EIF4A3-MLN51-UPF3B-MAGOH-Y14) protein complex from the CORUM Protein Complexes dataset.

Exon junction complex (F4A3-MLN51-UPF3B-MAGOH-Y14-PYM) Gene Set

From CORUM Protein Complexes

proteins in the Exon junction complex (F4A3-MLN51-UPF3B-MAGOH-Y14-PYM) protein complex from the CORUM Protein Complexes dataset.

Cell-cell junction complex (CDH1-CTNNB1) Gene Set

From CORUM Protein Complexes

proteins in the Cell-cell junction complex (CDH1-CTNNB1) protein complex from the CORUM Protein Complexes dataset.

neuromuscular junction disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease neuromuscular junction disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

rectosigmoid junction cancer Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease rectosigmoid junction cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

gastroesophageal junction adenocarcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease gastroesophageal junction adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

neuromuscular junction disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease neuromuscular junction disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

junction Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term junction in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

regulation of cell-substrate junction assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of cell-substrate junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of adherens junction organization Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of adherens junction organization biological process from the curated GO Biological Process Annotations 2015 dataset.

establishment of synaptic specificity at neuromuscular junction Gene Set

From GO Biological Process Annotations 2015

genes participating in the establishment of synaptic specificity at neuromuscular junction biological process from the curated GO Biological Process Annotations 2015 dataset.

cell-substrate junction assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the cell-substrate junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of synaptic growth at neuromuscular junction Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of synaptic growth at neuromuscular junction biological process from the curated GO Biological Process Annotations 2015 dataset.

cell-cell junction assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the cell-cell junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

protein localization to tight junction Gene Set

From GO Biological Process Annotations 2015

genes participating in the protein localization to tight junction biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of synaptic growth at neuromuscular junction Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of synaptic growth at neuromuscular junction biological process from the curated GO Biological Process Annotations 2015 dataset.

negative regulation of cell junction assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of cell junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

adherens junction maintenance Gene Set

From GO Biological Process Annotations 2015

genes participating in the adherens junction maintenance biological process from the curated GO Biological Process Annotations 2015 dataset.

apical junction assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the apical junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

cell-substrate adherens junction assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the cell-substrate adherens junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

cell junction assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the cell junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

adherens junction assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the adherens junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

paranodal junction assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the paranodal junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

cell junction maintenance Gene Set

From GO Biological Process Annotations 2015

genes participating in the cell junction maintenance biological process from the curated GO Biological Process Annotations 2015 dataset.

tight junction assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the tight junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of cell junction assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of cell junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

protein localization to adherens junction Gene Set

From GO Biological Process Annotations 2015

genes participating in the protein localization to adherens junction biological process from the curated GO Biological Process Annotations 2015 dataset.

cell junction organization Gene Set

From GO Biological Process Annotations 2015

genes participating in the cell junction organization biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of cell junction assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of cell junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

gap junction assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the gap junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

negative regulation of gap junction assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of gap junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of tight junction assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of tight junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

synaptic growth at neuromuscular junction Gene Set

From GO Biological Process Annotations 2015

genes participating in the synaptic growth at neuromuscular junction biological process from the curated GO Biological Process Annotations 2015 dataset.

neuromuscular junction development Gene Set

From GO Biological Process Annotations 2015

genes participating in the neuromuscular junction development biological process from the curated GO Biological Process Annotations 2015 dataset.

cell-cell junction organization Gene Set

From GO Biological Process Annotations 2015

genes participating in the cell-cell junction organization biological process from the curated GO Biological Process Annotations 2015 dataset.

atrial ventricular junction remodeling Gene Set

From GO Biological Process Annotations 2015

genes participating in the atrial ventricular junction remodeling biological process from the curated GO Biological Process Annotations 2015 dataset.

positive regulation of gap junction assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the positive regulation of gap junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

cell-cell junction maintenance Gene Set

From GO Biological Process Annotations 2015

genes participating in the cell-cell junction maintenance biological process from the curated GO Biological Process Annotations 2015 dataset.

cell-cell signaling involved in cell-cell junction organization Gene Set

From GO Biological Process Annotations 2015

genes participating in the cell-cell signaling involved in cell-cell junction organization biological process from the curated GO Biological Process Annotations 2015 dataset.

negative regulation of adherens junction organization Gene Set

From GO Biological Process Annotations 2015

genes participating in the negative regulation of adherens junction organization biological process from the curated GO Biological Process Annotations 2015 dataset.

protein localization to cell junction Gene Set

From GO Biological Process Annotations 2015

genes participating in the protein localization to cell junction biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of adherens junction organization Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of adherens junction organization biological process from the curated GO Biological Process Annotations 2015 dataset.

adherens junction organization Gene Set

From GO Biological Process Annotations 2015

genes participating in the adherens junction organization biological process from the curated GO Biological Process Annotations 2015 dataset.

regulation of gap junction assembly Gene Set

From GO Biological Process Annotations 2015

genes participating in the regulation of gap junction assembly biological process from the curated GO Biological Process Annotations 2015 dataset.

cell junction Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the cell junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

spot adherens junction Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the spot adherens junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

tight junction Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the tight junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

cell-substrate junction Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the cell-substrate junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

nucleus-vacuole junction Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the nucleus-vacuole junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

cell-cell junction Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the cell-cell junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

muscle tendon junction Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the muscle tendon junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

holliday junction resolvase complex Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the holliday junction resolvase complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.

apical junction complex Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the apical junction complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.

occluding junction Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the occluding junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

anchoring junction Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the anchoring junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

cell-cell adherens junction Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the cell-cell adherens junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

cell-substrate adherens junction Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the cell-substrate adherens junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

exon-exon junction complex Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the exon-exon junction complex cellular component from the curated GO Cellular Component Annotations 2015 dataset.

adherens junction Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the adherens junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

gap junction Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the gap junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

paranodal junction Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the paranodal junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

neuromuscular junction Gene Set

From GO Cellular Component Annotations 2015

proteins localized to the neuromuscular junction cellular component from the curated GO Cellular Component Annotations 2015 dataset.

gap junction hemi-channel activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the gap junction hemi-channel activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

gap junction channel activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the gap junction channel activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

double-strand/single-strand dna junction binding Gene Set

From GO Molecular Function Annotations 2015

genes performing the double-strand/single-strand dna junction binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.

crossover junction endodeoxyribonuclease activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the crossover junction endodeoxyribonuclease activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

gap junction channel activity involved in cell communication by electrical coupling Gene Set

From GO Molecular Function Annotations 2015

genes performing the gap junction channel activity involved in cell communication by electrical coupling molecular function from the curated GO Molecular Function Annotations 2015 dataset.

four-way junction helicase activity Gene Set

From GO Molecular Function Annotations 2015

genes performing the four-way junction helicase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.

gap junction channel activity involved in av node cell-bundle of his cell electrical coupling Gene Set

From GO Molecular Function Annotations 2015

genes performing the gap junction channel activity involved in av node cell-bundle of his cell electrical coupling molecular function from the curated GO Molecular Function Annotations 2015 dataset.

four-way junction dna binding Gene Set

From GO Molecular Function Annotations 2015

genes performing the four-way junction dna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.

gap junction channel activity involved in cardiac conduction electrical coupling Gene Set

From GO Molecular Function Annotations 2015

genes performing the gap junction channel activity involved in cardiac conduction electrical coupling molecular function from the curated GO Molecular Function Annotations 2015 dataset.

neuromuscular junction disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease neuromuscular junction disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

abnormality of the costochondral junction Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the costochondral junction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

enlargement of the costochondral junction Gene Set

From HPO Gene-Disease Associations

genes associated with the enlargement of the costochondral junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal synaptic transmission at the neuromuscular junction Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal synaptic transmission at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the costochondral junction Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the costochondral junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

generalized hypotonia due to defect at the neuromuscular junction Gene Set

From HPO Gene-Disease Associations

genes associated with the generalized hypotonia due to defect at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bulging of the costochondral junction Gene Set

From HPO Gene-Disease Associations

genes associated with the bulging of the costochondral junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Holliday junction recognition protein, HJURP Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Holliday junction recognition protein, HJURP protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Holliday junction regulator protein family C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Holliday junction regulator protein family C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tight junction protein ZO Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tight junction protein ZO protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Gap junction beta-5 protein (Cx30.3) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Gap junction beta-5 protein (Cx30.3) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Gap junction alpha-6 protein (Cx45) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Gap junction alpha-6 protein (Cx45) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Gap junction delta-2 protein (Cx36) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Gap junction delta-2 protein (Cx36) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Gap junction beta-4 protein (Cx31.1) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Gap junction beta-4 protein (Cx31.1) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Gap junction alpha-5 protein (Cx40) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Gap junction alpha-5 protein (Cx40) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Gap junction alpha-1 protein (Cx43), C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Gap junction alpha-1 protein (Cx43), C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Gap junction alpha-8 protein (Cx50) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Gap junction alpha-8 protein (Cx50) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Gap junction beta-1 protein (Cx32) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Gap junction beta-1 protein (Cx32) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Gap junction beta-2 protein (Cx26) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Gap junction beta-2 protein (Cx26) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neuromodulin gap junction N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neuromodulin gap junction N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Gap junction alpha-4 protein (Cx37) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Gap junction alpha-4 protein (Cx37) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Exon junction complex, Pym Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Exon junction complex, Pym protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tight junction-associated protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tight junction-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Gap junction protein, cysteine-rich domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Gap junction protein, cysteine-rich domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Gap junction beta-3 protein (Cx31) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Gap junction beta-3 protein (Cx31) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tight junction protein ZO-2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tight junction protein ZO-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tight junction protein ZO-3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tight junction protein ZO-3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Tight junction protein ZO-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Tight junction protein ZO-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Gap junction alpha-3 protein (Cx46) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Gap junction alpha-3 protein (Cx46) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Gap junction alpha-1 protein (Cx43) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Gap junction alpha-1 protein (Cx43) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

adherens junction Gene Set

From KEGG Pathways

proteins participating in the adherens junction pathway from the KEGG Pathways dataset.

tight junction Gene Set

From KEGG Pathways

proteins participating in the tight junction pathway from the KEGG Pathways dataset.

gap junction Gene Set

From KEGG Pathways

proteins participating in the gap junction pathway from the KEGG Pathways dataset.

cell junction Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the cell junction cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

tight junction Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the tight junction cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

cell-cell junction Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the cell-cell junction cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

occluding junction Gene Set

From LOCATE Curated Protein Localization Annotations

proteins localized to the occluding junction cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset.

esophagogastric junction metaplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the esophagogastric junction metaplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal epidermal-dermal junction morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal epidermal-dermal junction morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal paranodal axoglial junction morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal paranodal axoglial junction morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ureterovesical junction morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ureterovesical junction morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal podocyte slit junction morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal podocyte slit junction morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Posttranslational regulation of adherens junction stability and dissassembly Gene Set

From PID Pathways

proteins participating in the Posttranslational regulation of adherens junction stability and dissassembly pathway from the PID Pathways dataset.

E-cadherin signaling in the nascent adherens junction Gene Set

From PID Pathways

proteins participating in the E-cadherin signaling in the nascent adherens junction pathway from the PID Pathways dataset.

Stabilization and expansion of the E-cadherin adherens junction Gene Set

From PID Pathways

proteins participating in the Stabilization and expansion of the E-cadherin adherens junction pathway from the PID Pathways dataset.

Gap junction degradation Gene Set

From Reactome Pathways 2014

proteins participating in the Gap junction degradation pathway from the Reactome Pathways dataset.

Gap junction trafficking Gene Set

From Reactome Pathways 2014

proteins participating in the Gap junction trafficking pathway from the Reactome Pathways dataset.

Gap junction trafficking and regulation Gene Set

From Reactome Pathways 2014

proteins participating in the Gap junction trafficking and regulation pathway from the Reactome Pathways dataset.

Tight junction interactions Gene Set

From Reactome Pathways 2014

proteins participating in the Tight junction interactions pathway from the Reactome Pathways dataset.

Regulation of gap junction activity Gene Set

From Reactome Pathways 2014

proteins participating in the Regulation of gap junction activity pathway from the Reactome Pathways dataset.

Cell junction organization Gene Set

From Reactome Pathways 2014

proteins participating in the Cell junction organization pathway from the Reactome Pathways dataset.

Gap junction assembly Gene Set

From Reactome Pathways 2014

proteins participating in the Gap junction assembly pathway from the Reactome Pathways dataset.

Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) Gene Set

From Reactome Pathways 2014

proteins participating in the Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) pathway from the Reactome Pathways dataset.

Cell-cell junction organization Gene Set

From Reactome Pathways 2014

proteins participating in the Cell-cell junction organization pathway from the Reactome Pathways dataset.

Resolution of D-loop structures through Holliday junction intermediates Gene Set

From Reactome Pathways 2014

proteins participating in the Resolution of D-loop structures through Holliday junction intermediates pathway from the Reactome Pathways dataset.

Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) Gene Set

From Reactome Pathways 2014

proteins participating in the Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) pathway from the Reactome Pathways dataset.

gastroesophageal junction Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue gastroesophageal junction from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

gastroesophageal junction Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue gastroesophageal junction in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Diencephalic Mesencephalic Junction Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Diencephalic Mesencephalic Junction Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Generalized Hypotonia Due To Defect At The Neuromuscular Junction Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Generalized Hypotonia Due To Defect At The Neuromuscular Junction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Bulging Of The Costochondral Junction Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Bulging Of The Costochondral Junction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

Enlargement Of The Costochondral Junction Gene Set

From DisGeNET Gene-Phenotype Associations

genes associated with the phenotype Enlargement Of The Costochondral Junction in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.

cell junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the cell junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of bicellular tight junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of bicellular tight junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of synaptic assembly at neuromuscular junction Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of synaptic assembly at neuromuscular junction biological process from the curated GO Biological Process Annotations 2023 dataset.

cell-cell junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the cell-cell junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

tight junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the tight junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of bicellular tight junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of bicellular tight junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

neuromuscular junction development Gene Set

From GO Biological Process Annotations 2023

genes participating in the neuromuscular junction development biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of bicellular tight junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of bicellular tight junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

adherens junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the adherens junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of synaptic assembly at neuromuscular junction Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of synaptic assembly at neuromuscular junction biological process from the curated GO Biological Process Annotations 2023 dataset.

cell junction maintenance Gene Set

From GO Biological Process Annotations 2023

genes participating in the cell junction maintenance biological process from the curated GO Biological Process Annotations 2023 dataset.

bicellular tight junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the bicellular tight junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of cell junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of cell junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

apical junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the apical junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

gap junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the gap junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

cell-cell junction organization Gene Set

From GO Biological Process Annotations 2023

genes participating in the cell-cell junction organization biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of gap junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of gap junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of gap junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of gap junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

cell-cell junction maintenance Gene Set

From GO Biological Process Annotations 2023

genes participating in the cell-cell junction maintenance biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of tight junction disassembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of tight junction disassembly biological process from the curated GO Biological Process Annotations 2023 dataset.

adherens junction organization Gene Set

From GO Biological Process Annotations 2023

genes participating in the adherens junction organization biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of adherens junction organization Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of adherens junction organization biological process from the curated GO Biological Process Annotations 2023 dataset.

protein localization to cell-cell junction Gene Set

From GO Biological Process Annotations 2023

genes participating in the protein localization to cell-cell junction biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of protein localization to cell-cell junction Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of protein localization to cell-cell junction biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of protein localization to adherens junction Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of protein localization to adherens junction biological process from the curated GO Biological Process Annotations 2023 dataset.

paranodal junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the paranodal junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

cell-substrate junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the cell-substrate junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

establishment of synaptic specificity at neuromuscular junction Gene Set

From GO Biological Process Annotations 2023

genes participating in the establishment of synaptic specificity at neuromuscular junction biological process from the curated GO Biological Process Annotations 2023 dataset.

protein localization to bicellular tight junction Gene Set

From GO Biological Process Annotations 2023

genes participating in the protein localization to bicellular tight junction biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of gap junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of gap junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of adherens junction organization Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of adherens junction organization biological process from the curated GO Biological Process Annotations 2023 dataset.

protein localization to adherens junction Gene Set

From GO Biological Process Annotations 2023

genes participating in the protein localization to adherens junction biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of cell junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of cell junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

adherens junction maintenance Gene Set

From GO Biological Process Annotations 2023

genes participating in the adherens junction maintenance biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of neuromuscular junction development Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of neuromuscular junction development biological process from the curated GO Biological Process Annotations 2023 dataset.

protein localization to tricellular tight junction Gene Set

From GO Biological Process Annotations 2023

genes participating in the protein localization to tricellular tight junction biological process from the curated GO Biological Process Annotations 2023 dataset.

tricellular tight junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the tricellular tight junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

cell-substrate junction organization Gene Set

From GO Biological Process Annotations 2023

genes participating in the cell-substrate junction organization biological process from the curated GO Biological Process Annotations 2023 dataset.

protein localization to cell junction Gene Set

From GO Biological Process Annotations 2023

genes participating in the protein localization to cell junction biological process from the curated GO Biological Process Annotations 2023 dataset.

exon-exon junction complex disassembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the exon-exon junction complex disassembly biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of protein localization to cell-cell junction Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of protein localization to cell-cell junction biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of cell-substrate junction organization Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of cell-substrate junction organization biological process from the curated GO Biological Process Annotations 2023 dataset.

cell junction organization Gene Set

From GO Biological Process Annotations 2023

genes participating in the cell junction organization biological process from the curated GO Biological Process Annotations 2023 dataset.

tight junction organization Gene Set

From GO Biological Process Annotations 2023

genes participating in the tight junction organization biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of cell-substrate junction organization Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of cell-substrate junction organization biological process from the curated GO Biological Process Annotations 2023 dataset.

negative regulation of cell junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the negative regulation of cell junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

positive regulation of cell-substrate junction organization Gene Set

From GO Biological Process Annotations 2023

genes participating in the positive regulation of cell-substrate junction organization biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of neuromuscular junction development Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of neuromuscular junction development biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of cell-substrate junction assembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of cell-substrate junction assembly biological process from the curated GO Biological Process Annotations 2023 dataset.

cell-cell junction disassembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the cell-cell junction disassembly biological process from the curated GO Biological Process Annotations 2023 dataset.

cell junction disassembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the cell junction disassembly biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of tight junction disassembly Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of tight junction disassembly biological process from the curated GO Biological Process Annotations 2023 dataset.

regulation of adherens junction organization Gene Set

From GO Biological Process Annotations 2023

genes participating in the regulation of adherens junction organization biological process from the curated GO Biological Process Annotations 2023 dataset.

adherens junction Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the adherens junction cellular component from the curated GO Cellular Component Annotations 2023 dataset.

apical junction complex Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the apical junction complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.

tight junction Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the tight junction cellular component from the curated GO Cellular Component Annotations 2023 dataset.

cell-cell junction Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the cell-cell junction cellular component from the curated GO Cellular Component Annotations 2023 dataset.

bicellular tight junction Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the bicellular tight junction cellular component from the curated GO Cellular Component Annotations 2023 dataset.

neuromuscular junction Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the neuromuscular junction cellular component from the curated GO Cellular Component Annotations 2023 dataset.

tricellular tight junction Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the tricellular tight junction cellular component from the curated GO Cellular Component Annotations 2023 dataset.

gap junction Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the gap junction cellular component from the curated GO Cellular Component Annotations 2023 dataset.

cell-substrate junction Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the cell-substrate junction cellular component from the curated GO Cellular Component Annotations 2023 dataset.

spot adherens junction Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the spot adherens junction cellular component from the curated GO Cellular Component Annotations 2023 dataset.

muscle tendon junction Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the muscle tendon junction cellular component from the curated GO Cellular Component Annotations 2023 dataset.

paranodal junction Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the paranodal junction cellular component from the curated GO Cellular Component Annotations 2023 dataset.

Holliday junction resolvase complex Gene Set

From GO Cellular Component Annotations 2023

proteins localized to the Holliday junction resolvase complex cellular component from the curated GO Cellular Component Annotations 2023 dataset.

four-way junction DNA binding Gene Set

From GO Molecular Function Annotations 2023

genes performing the four-way junction DNA binding molecular function from the curated GO Molecular Function Annotations 2023 dataset.

crossover junction DNA endonuclease activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the crossover junction DNA endonuclease activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

gap junction channel activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the gap junction channel activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

gap junction channel activity involved in cell communication by electrical coupling Gene Set

From GO Molecular Function Annotations 2023

genes performing the gap junction channel activity involved in cell communication by electrical coupling molecular function from the curated GO Molecular Function Annotations 2023 dataset.

gap junction hemi-channel activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the gap junction hemi-channel activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

gap junction channel activity involved in cardiac conduction electrical coupling Gene Set

From GO Molecular Function Annotations 2023

genes performing the gap junction channel activity involved in cardiac conduction electrical coupling molecular function from the curated GO Molecular Function Annotations 2023 dataset.

gap junction channel activity involved in SA node cell-atrial cardiac muscle cell electrical coupling Gene Set

From GO Molecular Function Annotations 2023

genes performing the gap junction channel activity involved in SA node cell-atrial cardiac muscle cell electrical coupling molecular function from the curated GO Molecular Function Annotations 2023 dataset.

gap junction channel activity involved in atrial cardiac muscle cell-AV node cell electrical coupling Gene Set

From GO Molecular Function Annotations 2023

genes performing the gap junction channel activity involved in atrial cardiac muscle cell-AV node cell electrical coupling molecular function from the curated GO Molecular Function Annotations 2023 dataset.

gap junction channel activity involved in AV node cell-bundle of His cell electrical coupling Gene Set

From GO Molecular Function Annotations 2023

genes performing the gap junction channel activity involved in AV node cell-bundle of His cell electrical coupling molecular function from the curated GO Molecular Function Annotations 2023 dataset.

gap junction channel activity involved in bundle of His cell-Purkinje myocyte electrical coupling Gene Set

From GO Molecular Function Annotations 2023

genes performing the gap junction channel activity involved in bundle of His cell-Purkinje myocyte electrical coupling molecular function from the curated GO Molecular Function Annotations 2023 dataset.

gap junction channel activity involved in Purkinje myocyte-ventricular cardiac muscle cell electrical coupling Gene Set

From GO Molecular Function Annotations 2023

genes performing the gap junction channel activity involved in Purkinje myocyte-ventricular cardiac muscle cell electrical coupling molecular function from the curated GO Molecular Function Annotations 2023 dataset.

four-way junction helicase activity Gene Set

From GO Molecular Function Annotations 2023

genes performing the four-way junction helicase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset.

esophagogastric junction metaplasia Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the esophagogastric junction metaplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal podocyte slit junction morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal podocyte slit junction morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal paranodal axoglial junction morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal paranodal axoglial junction morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal epidermal-dermal junction morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal epidermal-dermal junction morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal forestomach-glandular stomach junction morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal forestomach-glandular stomach junction morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

abnormal ureterovesical junction morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal ureterovesical junction morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Esophagus - Gastroesophageal Junction Gene Set

From GTEx Tissue Gene Expression Profiles 2023

genes with high or low expression in Esophagus - Gastroesophageal Junction relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset.

Neuromuscular junction cell_Muscle_Mouse Gene Set

From CellMarker Gene-Cell Type Associations

genes associated with the Neuromuscular junction cell_Muscle_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.

Cell junction organization Gene Set

From Reactome Pathways 2024

proteins participating in the Cell junction organization pathway from the Reactome Pathways 2024 dataset.

Cell-cell junction organization Gene Set

From Reactome Pathways 2024

proteins participating in the Cell-cell junction organization pathway from the Reactome Pathways 2024 dataset.

Gap junction assembly Gene Set

From Reactome Pathways 2024

proteins participating in the Gap junction assembly pathway from the Reactome Pathways 2024 dataset.

Gap junction degradation Gene Set

From Reactome Pathways 2024

proteins participating in the Gap junction degradation pathway from the Reactome Pathways 2024 dataset.

Gap junction trafficking Gene Set

From Reactome Pathways 2024

proteins participating in the Gap junction trafficking pathway from the Reactome Pathways 2024 dataset.

Gap junction trafficking and regulation Gene Set

From Reactome Pathways 2024

proteins participating in the Gap junction trafficking and regulation pathway from the Reactome Pathways 2024 dataset.

Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) Gene Set

From Reactome Pathways 2024

proteins participating in the Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) pathway from the Reactome Pathways 2024 dataset.

Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) Gene Set

From Reactome Pathways 2024

proteins participating in the Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) pathway from the Reactome Pathways 2024 dataset.

Regulation of gap junction activity Gene Set

From Reactome Pathways 2024

proteins participating in the Regulation of gap junction activity pathway from the Reactome Pathways 2024 dataset.

Resolution of D-loop Structures through Holliday Junction Intermediates Gene Set

From Reactome Pathways 2024

proteins participating in the Resolution of D-loop Structures through Holliday Junction Intermediates pathway from the Reactome Pathways 2024 dataset.

SARS-CoV-1 targets PDZ proteins in cell-cell junction Gene Set

From Reactome Pathways 2024

proteins participating in the SARS-CoV-1 targets PDZ proteins in cell-cell junction pathway from the Reactome Pathways 2024 dataset.

SARS-CoV-2 targets PDZ proteins in cell-cell junction Gene Set

From Reactome Pathways 2024

proteins participating in the SARS-CoV-2 targets PDZ proteins in cell-cell junction pathway from the Reactome Pathways 2024 dataset.

Tight junction interactions Gene Set

From Reactome Pathways 2024

proteins participating in the Tight junction interactions pathway from the Reactome Pathways 2024 dataset.

cell junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the cell junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of bicellular tight junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of bicellular tight junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of synaptic assembly at neuromuscular junction Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of synaptic assembly at neuromuscular junction biological process from the curated GO Biological Process Annotations 2025 dataset.

cell-cell junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the cell-cell junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

tight junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the tight junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of bicellular tight junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of bicellular tight junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

neuromuscular junction development Gene Set

From GO Biological Process Annotations 2025

genes participating in the neuromuscular junction development biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of bicellular tight junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of bicellular tight junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

adherens junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the adherens junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of synaptic assembly at neuromuscular junction Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of synaptic assembly at neuromuscular junction biological process from the curated GO Biological Process Annotations 2025 dataset.

cell junction maintenance Gene Set

From GO Biological Process Annotations 2025

genes participating in the cell junction maintenance biological process from the curated GO Biological Process Annotations 2025 dataset.

cell-cell junction maintenance Gene Set

From GO Biological Process Annotations 2025

genes participating in the cell-cell junction maintenance biological process from the curated GO Biological Process Annotations 2025 dataset.

bicellular tight junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the bicellular tight junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of protein localization to cell-cell junction Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of protein localization to cell-cell junction biological process from the curated GO Biological Process Annotations 2025 dataset.

apical junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the apical junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of cell junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of cell junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

gap junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the gap junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

cell-cell junction organization Gene Set

From GO Biological Process Annotations 2025

genes participating in the cell-cell junction organization biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of gap junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of gap junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of tight junction disassembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of tight junction disassembly biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of gap junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of gap junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

adherens junction organization Gene Set

From GO Biological Process Annotations 2025

genes participating in the adherens junction organization biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of adherens junction organization Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of adherens junction organization biological process from the curated GO Biological Process Annotations 2025 dataset.

protein localization to cell-cell junction Gene Set

From GO Biological Process Annotations 2025

genes participating in the protein localization to cell-cell junction biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of protein localization to adherens junction Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of protein localization to adherens junction biological process from the curated GO Biological Process Annotations 2025 dataset.

paranodal junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the paranodal junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

cell-substrate junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the cell-substrate junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

establishment of synaptic specificity at neuromuscular junction Gene Set

From GO Biological Process Annotations 2025

genes participating in the establishment of synaptic specificity at neuromuscular junction biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of protein localization to adherens junction Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of protein localization to adherens junction biological process from the curated GO Biological Process Annotations 2025 dataset.

protein localization to bicellular tight junction Gene Set

From GO Biological Process Annotations 2025

genes participating in the protein localization to bicellular tight junction biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of gap junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of gap junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of adherens junction organization Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of adherens junction organization biological process from the curated GO Biological Process Annotations 2025 dataset.

tight junction organization Gene Set

From GO Biological Process Annotations 2025

genes participating in the tight junction organization biological process from the curated GO Biological Process Annotations 2025 dataset.

protein localization to adherens junction Gene Set

From GO Biological Process Annotations 2025

genes participating in the protein localization to adherens junction biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of cell junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of cell junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

adherens junction maintenance Gene Set

From GO Biological Process Annotations 2025

genes participating in the adherens junction maintenance biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of neuromuscular junction development Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of neuromuscular junction development biological process from the curated GO Biological Process Annotations 2025 dataset.

protein localization to tricellular tight junction Gene Set

From GO Biological Process Annotations 2025

genes participating in the protein localization to tricellular tight junction biological process from the curated GO Biological Process Annotations 2025 dataset.

tricellular tight junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the tricellular tight junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

cell-substrate junction organization Gene Set

From GO Biological Process Annotations 2025

genes participating in the cell-substrate junction organization biological process from the curated GO Biological Process Annotations 2025 dataset.

protein localization to cell junction Gene Set

From GO Biological Process Annotations 2025

genes participating in the protein localization to cell junction biological process from the curated GO Biological Process Annotations 2025 dataset.

exon-exon junction complex disassembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the exon-exon junction complex disassembly biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of protein localization to cell-cell junction Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of protein localization to cell-cell junction biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of cell-substrate junction organization Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of cell-substrate junction organization biological process from the curated GO Biological Process Annotations 2025 dataset.

cell junction organization Gene Set

From GO Biological Process Annotations 2025

genes participating in the cell junction organization biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of cell-substrate junction organization Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of cell-substrate junction organization biological process from the curated GO Biological Process Annotations 2025 dataset.

negative regulation of cell junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the negative regulation of cell junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

positive regulation of cell-substrate junction organization Gene Set

From GO Biological Process Annotations 2025

genes participating in the positive regulation of cell-substrate junction organization biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of neuromuscular junction development Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of neuromuscular junction development biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of cell-substrate junction assembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of cell-substrate junction assembly biological process from the curated GO Biological Process Annotations 2025 dataset.

cell-cell junction disassembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the cell-cell junction disassembly biological process from the curated GO Biological Process Annotations 2025 dataset.

cell junction disassembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the cell junction disassembly biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of tight junction disassembly Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of tight junction disassembly biological process from the curated GO Biological Process Annotations 2025 dataset.

regulation of adherens junction organization Gene Set

From GO Biological Process Annotations 2025

genes participating in the regulation of adherens junction organization biological process from the curated GO Biological Process Annotations 2025 dataset.

adherens junction Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the adherens junction cellular component from the curated GO Cellular Component Annotations 2025 dataset.

apical junction complex Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the apical junction complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.

tight junction Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the tight junction cellular component from the curated GO Cellular Component Annotations 2025 dataset.

cell-cell junction Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the cell-cell junction cellular component from the curated GO Cellular Component Annotations 2025 dataset.

bicellular tight junction Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the bicellular tight junction cellular component from the curated GO Cellular Component Annotations 2025 dataset.

neuromuscular junction Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the neuromuscular junction cellular component from the curated GO Cellular Component Annotations 2025 dataset.

tricellular tight junction Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the tricellular tight junction cellular component from the curated GO Cellular Component Annotations 2025 dataset.

gap junction Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the gap junction cellular component from the curated GO Cellular Component Annotations 2025 dataset.

cell-substrate junction Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the cell-substrate junction cellular component from the curated GO Cellular Component Annotations 2025 dataset.

spot adherens junction Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the spot adherens junction cellular component from the curated GO Cellular Component Annotations 2025 dataset.

muscle tendon junction Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the muscle tendon junction cellular component from the curated GO Cellular Component Annotations 2025 dataset.

paranodal junction Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the paranodal junction cellular component from the curated GO Cellular Component Annotations 2025 dataset.

Holliday junction resolvase complex Gene Set

From GO Cellular Component Annotations 2025

proteins localized to the Holliday junction resolvase complex cellular component from the curated GO Cellular Component Annotations 2025 dataset.

four-way junction DNA binding Gene Set

From GO Molecular Function Annotations 2025

genes performing the four-way junction DNA binding molecular function from the curated GO Molecular Function Annotations 2025 dataset.

crossover junction DNA endonuclease activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the crossover junction DNA endonuclease activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

gap junction channel activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the gap junction channel activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

gap junction channel activity involved in cell communication by electrical coupling Gene Set

From GO Molecular Function Annotations 2025

genes performing the gap junction channel activity involved in cell communication by electrical coupling molecular function from the curated GO Molecular Function Annotations 2025 dataset.

gap junction hemi-channel activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the gap junction hemi-channel activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

gap junction channel activity involved in cardiac conduction electrical coupling Gene Set

From GO Molecular Function Annotations 2025

genes performing the gap junction channel activity involved in cardiac conduction electrical coupling molecular function from the curated GO Molecular Function Annotations 2025 dataset.

gap junction channel activity involved in SA node cell-atrial cardiac muscle cell electrical coupling Gene Set

From GO Molecular Function Annotations 2025

genes performing the gap junction channel activity involved in SA node cell-atrial cardiac muscle cell electrical coupling molecular function from the curated GO Molecular Function Annotations 2025 dataset.

gap junction channel activity involved in atrial cardiac muscle cell-AV node cell electrical coupling Gene Set

From GO Molecular Function Annotations 2025

genes performing the gap junction channel activity involved in atrial cardiac muscle cell-AV node cell electrical coupling molecular function from the curated GO Molecular Function Annotations 2025 dataset.

gap junction channel activity involved in AV node cell-bundle of His cell electrical coupling Gene Set

From GO Molecular Function Annotations 2025

genes performing the gap junction channel activity involved in AV node cell-bundle of His cell electrical coupling molecular function from the curated GO Molecular Function Annotations 2025 dataset.

gap junction channel activity involved in bundle of His cell-Purkinje myocyte electrical coupling Gene Set

From GO Molecular Function Annotations 2025

genes performing the gap junction channel activity involved in bundle of His cell-Purkinje myocyte electrical coupling molecular function from the curated GO Molecular Function Annotations 2025 dataset.

gap junction channel activity involved in Purkinje myocyte-ventricular cardiac muscle cell electrical coupling Gene Set

From GO Molecular Function Annotations 2025

genes performing the gap junction channel activity involved in Purkinje myocyte-ventricular cardiac muscle cell electrical coupling molecular function from the curated GO Molecular Function Annotations 2025 dataset.

four-way junction helicase activity Gene Set

From GO Molecular Function Annotations 2025

genes performing the four-way junction helicase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset.

Neuromuscular junction disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores 2025

genes involed in the disease Neuromuscular junction disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.

Neuromuscular junction disease Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Neuromuscular junction disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Gastroesophageal junction adenocarcinoma Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Gastroesophageal junction adenocarcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Rectosigmoid junction cancer Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Rectosigmoid junction cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Rectosigmoid junction neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Rectosigmoid junction neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Gastroesophageal junction Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025

proteins co-occuring with the tissue Gastroesophageal junction in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.

Mitochondrial crista junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Mitochondrial crista junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Apical junction complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Apical junction complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Tight junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Tight junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Anchoring junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Anchoring junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

cell-cell junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the cell-cell junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Bicellular tight junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Bicellular tight junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Cell junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Cell junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Gap junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Gap junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

exon-exon junction complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the exon-exon junction complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

cell-substrate junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the cell-substrate junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Adherens junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Adherens junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Neuromuscular junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Neuromuscular junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Tricellular tight junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Tricellular tight junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Spot adherens junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Spot adherens junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Muscle tendon junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Muscle tendon junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Paranodal junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Paranodal junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

nucleus-vacuole junction Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the nucleus-vacuole junction cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

exon-exon junction subcomplex mago-y14 Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the exon-exon junction subcomplex mago-y14 cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Holliday junction resolvase complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores 2025

proteins localized to the Holliday junction resolvase complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.

Cell junction Gene Set

From COMPARTMENTS Experimental Protein Localization Evidence Scores 2025

proteins localized to the Cell junction cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 dataset.

cell-substrate junction Gene Set

From COMPARTMENTS Experimental Protein Localization Evidence Scores 2025

proteins localized to the cell-substrate junction cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 dataset.

Anchoring junction Gene Set

From COMPARTMENTS Experimental Protein Localization Evidence Scores 2025

proteins localized to the Anchoring junction cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 dataset.

Apical junction complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Apical junction complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Bicellular tight junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Bicellular tight junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Cell junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Cell junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Anchoring junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Anchoring junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

cell-cell junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the cell-cell junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Tight junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Tight junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Gap junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Gap junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

cell-substrate junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the cell-substrate junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Neuromuscular junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Neuromuscular junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Adherens junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Adherens junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Paranodal junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Paranodal junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Tricellular tight junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Tricellular tight junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

exon-exon junction complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the exon-exon junction complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Holliday junction resolvase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Holliday junction resolvase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Mitochondrial crista junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Mitochondrial crista junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Septate junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Septate junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Muscle tendon junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Muscle tendon junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

exon-exon junction subcomplex mago-y14 Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the exon-exon junction subcomplex mago-y14 cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

nucleus-vacuole junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the nucleus-vacuole junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Pleated septate junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Pleated septate junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Inhibitory neuromuscular junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Inhibitory neuromuscular junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Spot adherens junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Spot adherens junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Postsynapse of neuromuscular junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Postsynapse of neuromuscular junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Holliday junction helicase complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Holliday junction helicase complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Neuromuscular junction of somatic muscle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Neuromuscular junction of somatic muscle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Excitatory neuromuscular junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Excitatory neuromuscular junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Smooth septate junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the Smooth septate junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

host-symbiont bicellular tight junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the host-symbiont bicellular tight junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

bacterial-type flagellum hook-filament junction Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025

proteins co-occuring with the bacterial-type flagellum hook-filament junction cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.

Diencephalic-mesencephalic junction dysplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Diencephalic-mesencephalic junction dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Atrioventricular septal defect and common atrioventricular junction Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Atrioventricular septal defect and common atrioventricular junction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Diencephalic-mesencephalic junction dysplasia Gene Set

From ClinVar Gene-Phenotype Associations 2025

genes associated with the Diencephalic-mesencephalic junction dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Adherens junction Gene Set

From KEGG Pathways 2026

proteins participating in the Adherens junction pathway from the KEGG Pathways 2026 dataset.

Tight junction Gene Set

From KEGG Pathways 2026

proteins participating in the Tight junction pathway from the KEGG Pathways 2026 dataset.

Gap junction Gene Set

From KEGG Pathways 2026

proteins participating in the Gap junction pathway from the KEGG Pathways 2026 dataset.

Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital myotonia, autosomal dominant form Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital myotonia, autosomal dominant form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital adrenal hyperplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital adrenal hyperplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital human immunodeficiency virus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital human immunodeficiency virus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diarrhea 5, with tufting enteropathy, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diarrhea 5, with tufting enteropathy, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vertical talus, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vertical talus, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital generalized lipodystrophy type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital generalized lipodystrophy type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IV, congenital neuromuscular Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IV, congenital neuromuscular phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Facial paresis, hereditary congenital, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Facial paresis, hereditary congenital, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital glucose-galactose malabsorption Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital glucose-galactose malabsorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital sensory neuropathy with selective loss of small myelinated fibers Gene Set

From 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.

Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, actin, congenital, with cores Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, actin, congenital, with cores phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aphakia, congenital primary Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aphakia, congenital primary phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lipodystrophy, congenital generalized, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lipodystrophy, congenital generalized, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital contractural arachnodactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital contractural arachnodactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital absence of salivary gland Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital absence of salivary gland phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Merosin deficient congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Merosin deficient congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nystagmus 6, congenital, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nystagmus 6, congenital, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, autosomal dominant 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, autosomal dominant 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Afibrinogenemia, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Afibrinogenemia, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, congenital heart defects, and posterior embryotoxon Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Walker-Warburg congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Walker-Warburg congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibrosis of extraocular muscles, congenital, 3b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibrosis of extraocular muscles, congenital, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital amegakaryocytic thrombocytopenia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital amegakaryocytic thrombocytopenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, fast-channel Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, fast-channel phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, autosomal recessive congenital 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, autosomal recessive congenital 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diarrhea 3, secretory sodium, congenital, syndromic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diarrhea 3, secretory sodium, congenital, syndromic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia 3, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia 3, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital dyserythropoietic anemia, type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital dyserythropoietic anemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital adrenal hypoplasia, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital adrenal hypoplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lethal congenital contracture syndrome 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal congenital contracture syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital secretory diarrhea, chloride type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital secretory diarrhea, chloride type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination and Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibrosis of extraocular muscles, congenital, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibrosis of extraocular muscles, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibrosis of extraocular muscles, congenital, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibrosis of extraocular muscles, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Testicular anomalies with or without congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

LIPOPROTEIN(a) DEFICIENCY, CONGENITAL Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the LIPOPROTEIN(a) DEFICIENCY, CONGENITAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital short bowel syndrome, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital short bowel syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital heart disease, multiple types, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, slow-channel congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, slow-channel congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Indifference to pain, congenital, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Indifference to pain, congenital, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, autosomal dominant 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, autosomal dominant 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lethal congenital contractural syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal congenital contractural syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital heart defects, multiple types, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital heart defects, multiple types, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital erythropoietic porphyria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital erythropoietic porphyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

congenital neutropenia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the congenital neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypothyroidism, congenital, nongoitrous, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypothyroidism, congenital, nongoitrous, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypothyroidism, congenital, nongoitrous, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypothyroidism, congenital, nongoitrous, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypothyroidism, congenital, nongoitrous, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypothyroidism, congenital, nongoitrous, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1s Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1L Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, actin, congenital, with excess of thin myofilaments Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, actin, congenital, with excess of thin myofilaments phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Rett syndrome, congenital variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rett syndrome, congenital variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Eichsfeld type congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Eichsfeld type congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2L Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2k Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2k phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, congenital, with excess of muscle spindles Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, congenital, with excess of muscle spindles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital lactase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital lactase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital myotonia, autosomal recessive form Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital myotonia, autosomal recessive form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia 6, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia 6, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1Q Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1P Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1P phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1H Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, with tubular aggregates 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, with tubular aggregates 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1N Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Finnish congenital nephrotic syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Finnish congenital nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bile acid synthesis defect, congenital, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bile acid synthesis defect, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bile acid synthesis defect, congenital, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bile acid synthesis defect, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1v Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1v phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, congenital nuclear, autosomal recessive 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, congenital nuclear, autosomal recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, congenital nuclear, autosomal recessive 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, congenital nuclear, autosomal recessive 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepiphyseal dysplasia with congenital joint dislocations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepiphyseal dysplasia with congenital joint dislocations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adult i Blood Group with or without Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, congenital, compton-north Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, congenital, compton-north phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital cystic disease of liver Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital cystic disease of liver phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pancreatic agenesis and congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type Ix Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type Ix phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital order of glycosylation type 1r Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital order of glycosylation type 1r phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ullrich congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ullrich congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital dyserythropoietic anemia, type II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital dyserythropoietic anemia, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy, congenital hypomyelinating, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy, congenital hypomyelinating, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital central hypoventilation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital central hypoventilation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital ocular coloboma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital ocular coloboma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1K Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1K phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1O Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1O phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1G Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1y Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1y phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Digital clubbing, isolated congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Digital clubbing, isolated congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1u Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1u phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1t Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1t phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anti-plasmin deficiency, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anti-plasmin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Prothrombin deficiency, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Prothrombin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia 2, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital defect of folate absorption Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital defect of folate absorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia 4, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia 4, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lethal congenital contracture syndrome 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal congenital contracture syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital aniridia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital aniridia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital long QT syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital long QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital hyperammonemia, type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital hyperammonemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital exostosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital exostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glutamine deficiency, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glutamine deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital microvillous atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital microvillous atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Partial congenital absence of teeth Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Partial congenital absence of teeth phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 4A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 4A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 4B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital myasthenic syndrome, acetazolamide-responsive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital myasthenic syndrome, acetazolamide-responsive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glaucoma, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glaucoma, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular hypertrophy-cerebral syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular hypertrophy-cerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Stromal Corneal Dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital Stromal Corneal Dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital myopathy with fiber type disproportion Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital myopathy with fiber type disproportion phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Hyperinsulinism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Hyperinsulinism from the curated CTD Gene-Disease Associations dataset.

Cataract congenital Volkmann type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract congenital Volkmann type from the curated CTD Gene-Disease Associations dataset.

Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital adrenal hyperplasia due to 21 hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.

Congenital Hypothyroidism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Hypothyroidism from the curated CTD Gene-Disease Associations dataset.

Congenital bilateral aplasia of vas deferens Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital bilateral aplasia of vas deferens from the curated CTD Gene-Disease Associations dataset.

Congenital Abnormalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Abnormalities from the curated CTD Gene-Disease Associations dataset.

Anemia, Hemolytic, Congenital Nonspherocytic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Hemolytic, Congenital Nonspherocytic from the curated CTD Gene-Disease Associations dataset.

Night Blindness, Congenital Stationary, Autosomal Dominant 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 3 from the curated CTD Gene-Disease Associations dataset.

Hypothyroidism, Congenital, Nongoitrous, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 4 from the curated CTD Gene-Disease Associations dataset.

Leber Congenital Amaurosis 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leber Congenital Amaurosis 4 from the curated CTD Gene-Disease Associations dataset.

Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset.

Congenital idiopathic intestinal pseudoobstruction Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital idiopathic intestinal pseudoobstruction from the curated CTD Gene-Disease Associations dataset.

Vertical talus, congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Vertical talus, congenital from the curated CTD Gene-Disease Associations dataset.

Nystagmus 1, congenital, X- linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nystagmus 1, congenital, X- linked from the curated CTD Gene-Disease Associations dataset.

Facial paresis, hereditary, congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Facial paresis, hereditary, congenital from the curated CTD Gene-Disease Associations dataset.

Congenital anosmia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital anosmia from the curated CTD Gene-Disease Associations dataset.

Hypothyroidism, Congenital, Nongoitrous, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 5 from the curated CTD Gene-Disease Associations dataset.

Hyperferritinemia, hereditary, with congenital cataracts Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperferritinemia, hereditary, with congenital cataracts from the curated CTD Gene-Disease Associations dataset.

Ichthyosiform erythroderma, Brocq congenital, nonbullous form Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosiform erythroderma, Brocq congenital, nonbullous form from the curated CTD Gene-Disease Associations dataset.

Neutropenia, Severe Congenital, Autosomal Dominant 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.

Hernias, Diaphragmatic, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hernias, Diaphragmatic, Congenital from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder Of Glycosylation, Type IIF Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIF from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1A from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation, type 2C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation, type 2C from the curated CTD Gene-Disease Associations dataset.

Lethal Congenital Contracture Syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lethal Congenital Contracture Syndrome 2 from the curated CTD Gene-Disease Associations dataset.

Aphakia, congenital primary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aphakia, congenital primary from the curated CTD Gene-Disease Associations dataset.

Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.

Congenital thrombotic disease, due to Protein C deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset.

Nystagmus 2, congenital, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nystagmus 2, congenital, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Hypothyroidism, Congenital, Nongoitrous, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 3 from the curated CTD Gene-Disease Associations dataset.

Congenital contractural arachnodactyly Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital contractural arachnodactyly from the curated CTD Gene-Disease Associations dataset.

Lactase Deficiency, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lactase Deficiency, Congenital from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 2D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 2D from the curated CTD Gene-Disease Associations dataset.

Nystagmus 4, congenital, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nystagmus 4, congenital, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset.

Anti-plasmin deficiency, congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anti-plasmin deficiency, congenital from the curated CTD Gene-Disease Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq from the curated CTD Gene-Disease Associations dataset.

Muscular dystrophy congenital, merosin negative Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular dystrophy congenital, merosin negative from the curated CTD Gene-Disease Associations dataset.

Indifference to Pain, Congenital, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Indifference to Pain, Congenital, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Ptosis, Hereditary Congenital 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ptosis, Hereditary Congenital 1 from the curated CTD Gene-Disease Associations dataset.

Pain Insensitivity, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pain Insensitivity, Congenital from the curated CTD Gene-Disease Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi from the curated CTD Gene-Disease Associations dataset.

MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1G from the curated CTD Gene-Disease Associations dataset.

Congenital amegakaryocytic thrombocytopenia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital amegakaryocytic thrombocytopenia from the curated CTD Gene-Disease Associations dataset.

Adrenal Hyperplasia, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adrenal Hyperplasia, Congenital from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B from the curated CTD Gene-Disease Associations dataset.

Anemia, Hypoplastic, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Hypoplastic, Congenital from the curated CTD Gene-Disease Associations dataset.

Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset.

Lipodystrophy, Congenital Generalized Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lipodystrophy, Congenital Generalized from the curated CTD Gene-Disease Associations dataset.

Congenital hypertrichosis lanuginosa Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital hypertrichosis lanuginosa from the curated CTD Gene-Disease Associations dataset.

Leber Congenital Amaurosis 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leber Congenital Amaurosis 10 from the curated CTD Gene-Disease Associations dataset.

Hypothyroidism, Congenital, Nongoitrous, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 2 from the curated CTD Gene-Disease Associations dataset.

Myopathy, Congenital, Compton-North Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Congenital, Compton-North from the curated CTD Gene-Disease Associations dataset.

Leber Congenital Amaurosis 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leber Congenital Amaurosis 3 from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder of Glycosylation, Type Io Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder of Glycosylation, Type Io from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.

Congenital central hypoventilation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital central hypoventilation syndrome from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder Of Glycosylation, Type Im Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type Im from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder Of Glycosylation, Type In Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type In from the curated CTD Gene-Disease Associations dataset.

Cataract, Congenital Zonular, with Sutural Opacities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Congenital Zonular, with Sutural Opacities from the curated CTD Gene-Disease Associations dataset.

Lethal congenital contracture syndrome 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lethal congenital contracture syndrome 1 from the curated CTD Gene-Disease Associations dataset.

Microcoria, congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcoria, congenital from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.

Anemia, Hemolytic, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Hemolytic, Congenital from the curated CTD Gene-Disease Associations dataset.

Bile acid synthesis defect, congenital, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 2 from the curated CTD Gene-Disease Associations dataset.

Bile acid synthesis defect, congenital, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 4 from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, 1B from the curated CTD Gene-Disease Associations dataset.

Leber Congenital Amaurosis 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leber Congenital Amaurosis 14 from the curated CTD Gene-Disease Associations dataset.

ADRENAL HYPOPLASIA, CONGENITAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ADRENAL HYPOPLASIA, CONGENITAL from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1H from the curated CTD Gene-Disease Associations dataset.

Ptosis, Hereditary Congenital 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ptosis, Hereditary Congenital 2 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 from the curated CTD Gene-Disease Associations dataset.

Diarrhea 4, Malabsorptive, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diarrhea 4, Malabsorptive, Congenital from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1J Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1J from the curated CTD Gene-Disease Associations dataset.

CAPILLARY MALFORMATIONS, CONGENITAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CAPILLARY MALFORMATIONS, CONGENITAL from the curated CTD Gene-Disease Associations dataset.

Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1B from the curated CTD Gene-Disease Associations dataset.

Nephrosis, congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nephrosis, congenital from the curated CTD Gene-Disease Associations dataset.

Neutropenia, Severe Congenital, Autosomal Dominant 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Dominant 1 from the curated CTD Gene-Disease Associations dataset.

GLAUCOMA 3, PRIMARY CONGENITAL, C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GLAUCOMA 3, PRIMARY CONGENITAL, C from the curated CTD Gene-Disease Associations dataset.

Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 2A from the curated CTD Gene-Disease Associations dataset.

ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 2E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 2E from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Merosin-Positive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Merosin-Positive from the curated CTD Gene-Disease Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip from the curated CTD Gene-Disease Associations dataset.

Myopathies, Structural, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathies, Structural, Congenital from the curated CTD Gene-Disease Associations dataset.

Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism from the curated CTD Gene-Disease Associations dataset.

ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.

Bile acid synthesis defect, congenital, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 1 from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1F from the curated CTD Gene-Disease Associations dataset.

Cataract, Autosomal Recessive Congenital 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Autosomal Recessive Congenital 3 from the curated CTD Gene-Disease Associations dataset.

Congenital myasthenic syndrome with episodic apnea Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital myasthenic syndrome with episodic apnea from the curated CTD Gene-Disease Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj from the curated CTD Gene-Disease Associations dataset.

Preauricular Fistulae, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Preauricular Fistulae, Congenital from the curated CTD Gene-Disease Associations dataset.

Leber Congenital Amaurosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leber Congenital Amaurosis from the curated CTD Gene-Disease Associations dataset.

Lower Extremity Deformities, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lower Extremity Deformities, Congenital from the curated CTD Gene-Disease Associations dataset.

Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.

NYSTAGMUS 5, CONGENITAL, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NYSTAGMUS 5, CONGENITAL, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Night blindness, congenital stationary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Night blindness, congenital stationary from the curated CTD Gene-Disease Associations dataset.

Fibrosis of Extraocular Muscles, Congenital, 3B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibrosis of Extraocular Muscles, Congenital, 3B from the curated CTD Gene-Disease Associations dataset.

Sucrase-isomaltase deficiency, congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sucrase-isomaltase deficiency, congenital from the curated CTD Gene-Disease Associations dataset.

Congenital myasthenic syndrome ib Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital myasthenic syndrome ib from the curated CTD Gene-Disease Associations dataset.

Polycythemia, primary familial and congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycythemia, primary familial and congenital from the curated CTD Gene-Disease Associations dataset.

Marie Unna congenital hypotrichosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Marie Unna congenital hypotrichosis from the curated CTD Gene-Disease Associations dataset.

NYSTAGMUS 6, CONGENITAL, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NYSTAGMUS 6, CONGENITAL, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Nystagmus 3, congenital, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nystagmus 3, congenital, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails from the curated CTD Gene-Disease Associations dataset.

Leber Congenital Amaurosis 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leber Congenital Amaurosis 12 from the curated CTD Gene-Disease Associations dataset.

Leber Congenital Amaurosis 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leber Congenital Amaurosis 13 from the curated CTD Gene-Disease Associations dataset.

Congenital atransferrinemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital atransferrinemia from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type II Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type II from the curated CTD Gene-Disease Associations dataset.

Fibrosis Of Extraocular Muscles, Congenital, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 2 from the curated CTD Gene-Disease Associations dataset.

Neutropenia, Severe Congenital, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, Severe Congenital, X-Linked from the curated CTD Gene-Disease Associations dataset.

ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR from the curated CTD Gene-Disease Associations dataset.

RETT SYNDROME, CONGENITAL VARIANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RETT SYNDROME, CONGENITAL VARIANT from the curated CTD Gene-Disease Associations dataset.

Myasthenic syndrome, congenital, postsynaptic slow-channel Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myasthenic syndrome, congenital, postsynaptic slow-channel from the curated CTD Gene-Disease Associations dataset.

Nystagmus, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nystagmus, Congenital from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1K Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1K from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1L Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1L from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1C from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1E from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1D from the curated CTD Gene-Disease Associations dataset.

Myasthenic Syndromes, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myasthenic Syndromes, Congenital from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Congenital Stromal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Congenital Stromal from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.

Hand Deformities, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hand Deformities, Congenital from the curated CTD Gene-Disease Associations dataset.

PROTHROMBIN DEFICIENCY, CONGENITAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PROTHROMBIN DEFICIENCY, CONGENITAL from the curated CTD Gene-Disease Associations dataset.

LEBER CONGENITAL AMAUROSIS 15 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease LEBER CONGENITAL AMAUROSIS 15 from the curated CTD Gene-Disease Associations dataset.

Diarrhea 3, Secretory Sodium, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diarrhea 3, Secretory Sodium, Congenital from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation, type 2G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation, type 2G from the curated CTD Gene-Disease Associations dataset.

Limb Deformities, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Limb Deformities, Congenital from the curated CTD Gene-Disease Associations dataset.

Pancreatic Agenesis, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pancreatic Agenesis, Congenital from the curated CTD Gene-Disease Associations dataset.

Hypertrichosis congenital generalized X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertrichosis congenital generalized X-linked from the curated CTD Gene-Disease Associations dataset.

Nail dysplasia, isolated congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nail dysplasia, isolated congenital from the curated CTD Gene-Disease Associations dataset.

Foot Deformities, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Foot Deformities, Congenital from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.

Lethal Congenital Contractural Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lethal Congenital Contractural Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

Cataract, Congenital Nuclear, Autosomal Recessive 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Congenital Nuclear, Autosomal Recessive 1 from the curated CTD Gene-Disease Associations dataset.

Heart Defects, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heart Defects, Congenital from the curated CTD Gene-Disease Associations dataset.

Glaucoma 3, Primary Congenital, D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma 3, Primary Congenital, D from the curated CTD Gene-Disease Associations dataset.

Glaucoma 3, Primary Congenital, A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma 3, Primary Congenital, A from the curated CTD Gene-Disease Associations dataset.

Adrenal hyperplasia, congenital, type 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adrenal hyperplasia, congenital, type 5 from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, Congenital Nonprogressive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, Congenital Nonprogressive from the curated CTD Gene-Disease Associations dataset.

Cataract, congenital, with microcornea or slight microphthalmia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, congenital, with microcornea or slight microphthalmia from the curated CTD Gene-Disease Associations dataset.

Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital adrenal hyperplasia due to 11-Beta-hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.

Lipoid congenital adrenal hyperplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lipoid congenital adrenal hyperplasia from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 from the curated CTD Gene-Disease Associations dataset.

Myasthenic Syndrome, Congenital, Fast-Channel Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myasthenic Syndrome, Congenital, Fast-Channel from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder Of Glycosylation, Type IIH Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIH from the curated CTD Gene-Disease Associations dataset.

Glutamine deficiency, congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glutamine deficiency, congenital from the curated CTD Gene-Disease Associations dataset.

Retinal Nonattachment, Nonsyndromic Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Retinal Nonattachment, Nonsyndromic Congenital from the curated CTD Gene-Disease Associations dataset.

SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPONDYLOEPIPHYSEAL DYSPLASIA WITH CONGENITAL JOINT DISLOCATIONS from the curated CTD Gene-Disease Associations dataset.

MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

Woolly hair, congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Woolly hair, congenital from the curated CTD Gene-Disease Associations dataset.

Glycogen Storage Disease of Heart, Lethal Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glycogen Storage Disease of Heart, Lethal Congenital from the curated CTD Gene-Disease Associations dataset.

Cataract, Congenital Nuclear, Autosomal Recessive 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Congenital Nuclear, Autosomal Recessive 3 from the curated CTD Gene-Disease Associations dataset.

Diarrhea 5, With Tufting Enteropathy, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diarrhea 5, With Tufting Enteropathy, Congenital from the curated CTD Gene-Disease Associations dataset.

Afibrinogenemia congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Afibrinogenemia congenital from the curated CTD Gene-Disease Associations dataset.

T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease T-cell immunodeficiency, congenital alopecia and nail dystrophy from the curated CTD Gene-Disease Associations dataset.

CATARACT, CONGENITAL OR JUVENILE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CATARACT, CONGENITAL OR JUVENILE from the curated CTD Gene-Disease Associations dataset.

Night Blindness, Congenital Stationary, Autosomal Dominant 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.

Cataract, Congenital Nuclear, Autosomal Recessive 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Congenital Nuclear, Autosomal Recessive 2 from the curated CTD Gene-Disease Associations dataset.

Lipodystrophy, Congenital Generalized, Type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lipodystrophy, Congenital Generalized, Type 3 from the curated CTD Gene-Disease Associations dataset.

Lipodystrophy, Congenital Generalized, Type 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lipodystrophy, Congenital Generalized, Type 4 from the curated CTD Gene-Disease Associations dataset.

Night Blindness, Congenital Stationary, Autosomal Dominant 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 1 from the curated CTD Gene-Disease Associations dataset.

Anemia, Dyserythropoietic, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Dyserythropoietic, Congenital from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder Of Glycosylation, Type IIB Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIB from the curated CTD Gene-Disease Associations dataset.

Neutropenia, Severe Congenital, Autosomal Recessive 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Recessive 3 from the curated CTD Gene-Disease Associations dataset.

Neutropenia, Severe Congenital, Autosomal Recessive 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Recessive 4 from the curated CTD Gene-Disease Associations dataset.

Hyperostosis, Cortical, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperostosis, Cortical, Congenital from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Lmna-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Lmna-Related from the curated CTD Gene-Disease Associations dataset.

congenital afibrinogenemia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease congenital afibrinogenemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital disorder of glycosylation Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease congenital disorder of glycosylation from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital heart disease Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease congenital heart disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

ullrich congenital muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease ullrich congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital diaphragmatic hernia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease congenital diaphragmatic hernia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

fukuyama congenital muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease fukuyama congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital dyserythropoietic anemia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease congenital dyserythropoietic anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

severe congenital neutropenia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease severe congenital neutropenia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital generalized lipodystrophy Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease congenital generalized lipodystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital hemolytic anemia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease congenital hemolytic anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital structural myopathy Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease congenital structural myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital nervous system abnormality Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease congenital nervous system abnormality from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital hypoplastic anemia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease congenital hypoplastic anemia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital muscular dystrophy Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease congenital muscular dystrophy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital hypothyroidism Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease congenital hypothyroidism from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital myasthenic syndrome Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease congenital myasthenic syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

leber congenital amaurosis Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease leber congenital amaurosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital stationary night blindness Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease congenital stationary night blindness from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

congenital ichthyosiform erythroderma Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease congenital ichthyosiform erythroderma from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

late congenital syphilis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease late congenital syphilis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

congenital disorder of glycosylation Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease congenital disorder of glycosylation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

congenital disorder of glycosylation type ii Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease congenital disorder of glycosylation type ii in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

congenital intrinsic factor deficiency Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease congenital intrinsic factor deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

congenital generalized lipodystrophy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease congenital generalized lipodystrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

congenital structural myopathy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease congenital structural myopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

congenital nervous system abnormality Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease congenital nervous system abnormality in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

congenital afibrinogenemia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease congenital afibrinogenemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

congenital granular cell tumor Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease congenital granular cell tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

congenital hypogammaglobulinemia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease congenital hypogammaglobulinemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

congenital syphilis Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease congenital syphilis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.