Name

MANF Gene

mesencephalic astrocyte-derived neurotrophic factor

The protein encoded by this gene is localized in the endoplasmic reticulum (ER) and golgi, and is also secreted. Reducing expression of this gene increases susceptibility to ER stress-induced death and results in cell proliferation. Activity of this protein is important in promoting the survival of dopaminergic neurons. The presence of polymorphisms in the N-terminal arginine-rich region, including a specific mutation that changes an ATG start codon to AGG, have been reported in a variety of solid tumors; however, these polymorphisms were later shown to exist in normal tissues and are thus no longer thought to be tumor-related. [provided by RefSeq, Apr 2014]

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]

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.

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.

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.

diencephalic neoplasm Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

Diencephalic Neoplasm Gene Set

From DisGeNET Gene-Disease Associations

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

Diencephalic neoplasm Gene Set

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

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

Diencephalic astrocytoma Gene Set

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

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

r1 part of the 'mesencephalic' trigeminal nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in r1 part of the 'mesencephalic' trigeminal nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

isthmic part of mesencephalic trigeminal nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in isthmic part of mesencephalic trigeminal nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

mesencephalic Gene Set

From GeneRIF Biological Term Annotations

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

absent mesencephalic trigeminal nucleus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent mesencephalic trigeminal nucleus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small mesencephalic trigeminal nucleus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small mesencephalic trigeminal nucleus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal trigeminal v mesencephalic nucleus morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal trigeminal v mesencephalic nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Mesencephalic Neoplasms Gene Set

From DisGeNET Gene-Disease Associations

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

abnormal trigeminal V mesencephalic nucleus morphology Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the abnormal trigeminal V mesencephalic nucleus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

absent mesencephalic trigeminal nucleus Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the absent mesencephalic trigeminal nucleus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

small mesencephalic trigeminal nucleus Gene Set

From MGI Mouse Phenotype Associations 2023

gene mutations causing the small mesencephalic trigeminal nucleus phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

carcinoma, squamous cell; cervical dysplasia; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; squamous cell carcinoma; tumor virus infections; uterine cervical dysplasia; uterine cervical neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, squamous cell; cervical dysplasia; cervical intraepithelial neoplasia; cervical neoplasm; papillomavirus infections; squamous cell carcinoma; tumor virus infections; uterine cervical dysplasia; uterine cervical neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia 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.

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.

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.

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.

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.

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 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.

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.

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 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.

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.

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.

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.

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.

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.

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.

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.

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 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 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 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.

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.

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.

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.

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.

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.

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.

Frontometaphyseal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Frontometaphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Czech dysplasia metatarsal type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Czech dysplasia metatarsal type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epiphyseal dysplasia, multiple, 3, with myopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epiphyseal dysplasia, multiple, 3, with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloperipheral dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloperipheral dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Wolcott-Rallison dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Wolcott-Rallison dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniodiaphyseal dysplasia, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniodiaphyseal dysplasia, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypohidrotic X-linked ectodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypohidrotic X-linked ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive pseudorheumatoid dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive pseudorheumatoid dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteoglophonic dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteoglophonic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gracile bone dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gracile bone dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Frontonasal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Frontonasal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondylometaphyseal dysplasia, Kozlowski type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylometaphyseal dysplasia, Kozlowski type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Odontoonychodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Odontoonychodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepimetaphyseal dysplasia with multiple dislocations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepimetaphyseal dysplasia with multiple dislocations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal-hepatic-pancreatic dysplasia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal-hepatic-pancreatic dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acampomelic campomelic dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acampomelic campomelic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia/short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia/short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepimetaphyseal dysplasia, Missouri type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepimetaphyseal dysplasia, Missouri type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypohidrotic ectodermal dysplasia with immune deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypohidrotic ectodermal dysplasia with immune deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofrontonasal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofrontonasal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anhidrotic ectodermal dysplasia with immune deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anhidrotic ectodermal dysplasia with immune deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepiphyseal dysplasia, kimberley type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepiphyseal dysplasia, kimberley type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 11 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cardiac valvular dysplasia, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cardiac valvular dysplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Trichorhinophalangeal dysplasia type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Trichorhinophalangeal dysplasia type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diastrophic dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diastrophic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thanatophoric dysplasia type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thanatophoric dysplasia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diaphyseal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diaphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive hypohidrotic ectodermal dysplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive hypohidrotic ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cleidocranial dysplasia, forme fruste, with brachydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cleidocranial dysplasia, forme fruste, with brachydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniometaphyseal dysplasia, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniometaphyseal dysplasia, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Schneckenbecken dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Schneckenbecken dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acromicric dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acromicric dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Terminal osseous dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Terminal osseous dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vitreoretinopathy with phalangeal epiphyseal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vitreoretinopathy with phalangeal epiphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acromesomelic dysplasia Maroteaux type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acromesomelic dysplasia Maroteaux type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Rapp-Hodgkin ectodermal dysplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rapp-Hodgkin ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Schimke immunoosseous dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Schimke immunoosseous dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Acrocapitofemoral dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Acrocapitofemoral dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hay-Wells syndrome of ectodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hay-Wells syndrome of ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Oculodentodigital dysplasia, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Oculodentodigital dysplasia, autosomal recessive 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.

Short-rib thoracic dysplasia 10 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Greenberg dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Greenberg dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Boomerang dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Boomerang dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniolenticulosutural dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniolenticulosutural dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Oculodentodigital dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Oculodentodigital dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Desbuquois dysplasia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Desbuquois dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia, complex, with other brain malformations 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia, complex, with other brain malformations 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia, complex, with other brain malformations 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia, complex, with other brain malformations 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia, complex, with other brain malformations 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia, complex, with other brain malformations 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia, complex, with other brain malformations 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia, complex, with other brain malformations 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia, complex, with other brain malformations 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia, complex, with other brain malformations 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bent bone dysplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bent bone dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylometaphyseal dysplasia with cone-rod dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chondroectodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chondroectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ischiopatellar dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ischiopatellar dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Geleophysic dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Geleophysic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autoimmune polyglandular syndrome type 1, with reversible metaphyseal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autoimmune polyglandular syndrome type 1, with reversible metaphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Geleophysic dysplasia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Geleophysic dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepimetaphyseal dysplasia, Aggrecan type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepimetaphyseal dysplasia, Aggrecan type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alveolar capillary dysplasia with misalignment of pulmonary veins Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alveolar capillary dysplasia with misalignment of pulmonary veins phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Brachyrachia (short spine dysplasia) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Brachyrachia (short spine dysplasia) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cortical dysplasia-focal epilepsy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cortical dysplasia-focal epilepsy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepimetaphyseal dysplasia Strudwick type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepimetaphyseal dysplasia Strudwick type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 3 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Septo-optic dysplasia sequence Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Septo-optic dysplasia sequence phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepiphyseal dysplasia Maroteaux type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepiphyseal dysplasia Maroteaux type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondylo-megaepiphyseal-metaphyseal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylo-megaepiphyseal-metaphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cranioectodermal dysplasia 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cranioectodermal dysplasia 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cranioectodermal dysplasia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cranioectodermal dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cranioectodermal dysplasia 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cranioectodermal dysplasia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epiphyseal dysplasia, multiple, with myopia and conductive deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epiphyseal dysplasia, multiple, with myopia and conductive deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cranioectodermal dysplasia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cranioectodermal dysplasia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibrous dysplasia of jaw Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibrous dysplasia of jaw phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Smith McCort dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Smith McCort dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepiphyseal dysplasia congenita Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepiphyseal dysplasia congenita phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple epiphyseal dysplasia 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple epiphyseal dysplasia 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple epiphyseal dysplasia 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple epiphyseal dysplasia 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple epiphyseal dysplasia 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple epiphyseal dysplasia 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia skin fragility syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia skin fragility syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepimetaphyseal dysplasia, pakistani type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepimetaphyseal dysplasia, pakistani type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Kniest dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Kniest dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Otospondylomegaepiphyseal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Otospondylomegaepiphyseal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondylometaepiphyseal dysplasia short limb-hand type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylometaepiphyseal dysplasia short limb-hand type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia-syndactyly syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia-syndactyly syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Metatrophic dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Metatrophic dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Frontonasal dysplasia 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Frontonasal dysplasia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Frontonasal dysplasia 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Frontonasal dysplasia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hidrotic ectodermal dysplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hidrotic ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dyssegmental dysplasia Gene Set

From CTD Gene-Disease Associations

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

Frontometaphyseal dysplasia Gene Set

From CTD Gene-Disease Associations

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

DEVELOPMENTAL DYSPLASIA OF THE HIP 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEVELOPMENTAL DYSPLASIA OF THE HIP 1 from the curated CTD Gene-Disease Associations dataset.

GNATHODIAPHYSEAL DYSPLASIA Gene Set

From CTD Gene-Disease Associations

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

Ectodermal Dysplasia 3, Anhidrotic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal Dysplasia 3, Anhidrotic from the curated CTD Gene-Disease Associations dataset.

Acrocapitofemoral Dysplasia Gene Set

From CTD Gene-Disease Associations

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

Thanatophoric dysplasia, type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thanatophoric dysplasia, type 2 from the curated CTD Gene-Disease Associations dataset.

Cardiac valvular dysplasia, X-linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiac valvular dysplasia, X-linked from the curated CTD Gene-Disease Associations dataset.

GREENBERG DYSPLASIA Gene Set

From CTD Gene-Disease Associations

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

Craniolenticulosutural Dysplasia Gene Set

From CTD Gene-Disease Associations

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

Mandibuloacral dysplasia with type B lipodystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mandibuloacral dysplasia with type B lipodystrophy from the curated CTD Gene-Disease Associations dataset.

CRANIOECTODERMAL DYSPLASIA 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CRANIOECTODERMAL DYSPLASIA 2 from the curated CTD Gene-Disease Associations dataset.

ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2 from the curated CTD Gene-Disease Associations dataset.

Focal cortical dysplasia of Taylor Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Focal cortical dysplasia of Taylor from the curated CTD Gene-Disease Associations dataset.

Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema from the curated CTD Gene-Disease Associations dataset.

Multicystic renal dysplasia, bilateral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Multicystic renal dysplasia, bilateral from the curated CTD Gene-Disease Associations dataset.

Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal Dysplasia, Multiple, with Myopia and Conductive Deafness from the curated CTD Gene-Disease Associations dataset.

Cranioectodermal Dysplasia Gene Set

From CTD Gene-Disease Associations

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

TERMINAL OSSEOUS DYSPLASIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TERMINAL OSSEOUS DYSPLASIA from the curated CTD Gene-Disease Associations dataset.

Thanatophoric Dysplasia, Type I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thanatophoric Dysplasia, Type I from the curated CTD Gene-Disease Associations dataset.

Acromicric dysplasia Gene Set

From CTD Gene-Disease Associations

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

Langer mesomelic dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Langer mesomelic dysplasia from the curated CTD Gene-Disease Associations dataset.

Cleidocranial Dysplasia Gene Set

From CTD Gene-Disease Associations

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

FRONTONASAL DYSPLASIA 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FRONTONASAL DYSPLASIA 1 from the curated CTD Gene-Disease Associations dataset.

FRONTONASAL DYSPLASIA 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FRONTONASAL DYSPLASIA 2 from the curated CTD Gene-Disease Associations dataset.

Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Bronchopulmonary Dysplasia Gene Set

From CTD Gene-Disease Associations

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

Spondylo-Megaepiphyseal-Metaphyseal Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondylo-Megaepiphyseal-Metaphyseal Dysplasia from the curated CTD Gene-Disease Associations dataset.

Spondyloepiphyseal Dysplasia Tarda, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondyloepiphyseal Dysplasia Tarda, X-Linked from the curated CTD Gene-Disease Associations dataset.

Polyostotic osteolytic dysplasia, hereditary expansile Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polyostotic osteolytic dysplasia, hereditary expansile from the curated CTD Gene-Disease Associations dataset.

FRONTONASAL DYSPLASIA 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FRONTONASAL DYSPLASIA 3 from the curated CTD Gene-Disease Associations dataset.

Schimke immunoosseous dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Schimke immunoosseous dysplasia from the curated CTD Gene-Disease Associations dataset.

Ectodermal Dysplasia Gene Set

From CTD Gene-Disease Associations

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

ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE from the curated CTD Gene-Disease Associations dataset.

Immunodeficiency without anhidrotic ectodermal dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Immunodeficiency without anhidrotic ectodermal dysplasia from the curated CTD Gene-Disease Associations dataset.

Craniofrontonasal dysplasia Gene Set

From CTD Gene-Disease Associations

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

Oculodentodigital Dysplasia Gene Set

From CTD Gene-Disease Associations

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

Anal sphincter dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anal sphincter dysplasia from the curated CTD Gene-Disease Associations dataset.

Platyspondylic Lethal Skeletal Dysplasia, Torrance Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Platyspondylic Lethal Skeletal Dysplasia, Torrance Type from the curated CTD Gene-Disease Associations dataset.

Anauxetic dysplasia Gene Set

From CTD Gene-Disease Associations

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

Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Skeletal Dysplasia, and Abducens Palsy from the curated CTD Gene-Disease Associations dataset.

Hypopituitarism and septooptic 'dysplasia' Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypopituitarism and septooptic 'dysplasia' from the curated CTD Gene-Disease Associations dataset.

Odontoonychodermal dysplasia Gene Set

From CTD Gene-Disease Associations

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

Spondylometaphyseal dysplasia, Kozlowski type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondylometaphyseal dysplasia, Kozlowski type from the curated CTD Gene-Disease Associations dataset.

Cortical Dysplasia-Focal Epilepsy Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cortical Dysplasia-Focal Epilepsy Syndrome from the curated CTD Gene-Disease Associations dataset.

Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 from the curated CTD Gene-Disease Associations dataset.

SPONDYLOPERIPHERAL DYSPLASIA Gene Set

From CTD Gene-Disease Associations

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

RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 from the curated CTD Gene-Disease Associations dataset.

Spondyloepiphyseal Dysplasia, Kimberley Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondyloepiphyseal Dysplasia, Kimberley Type from the curated CTD Gene-Disease Associations dataset.

Craniometaphyseal Dysplasia, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Craniometaphyseal Dysplasia, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Schneckenbecken dysplasia Gene Set

From CTD Gene-Disease Associations

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

Thanatophoric Dysplasia Gene Set

From CTD Gene-Disease Associations

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

Ectodermal dysplasia/ skin fragility syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal dysplasia/ skin fragility syndrome from the curated CTD Gene-Disease Associations dataset.

Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Ghosal Hematodiaphyseal Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ghosal Hematodiaphyseal Dysplasia from the curated CTD Gene-Disease Associations dataset.

Smith-McCort Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Smith-McCort Dysplasia from the curated CTD Gene-Disease Associations dataset.

Diastrophic dysplasia Gene Set

From CTD Gene-Disease Associations

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

Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 from the curated CTD Gene-Disease Associations dataset.

Fibrous Dysplasia, Polyostotic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibrous Dysplasia, Polyostotic from the curated CTD Gene-Disease Associations dataset.

RETINAL DYSPLASIA, PRIMARY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RETINAL DYSPLASIA, PRIMARY from the curated CTD Gene-Disease Associations dataset.

SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPONDYLOEPIPHYSEAL DYSPLASIA, MAROTEAUX TYPE from the curated CTD Gene-Disease Associations dataset.

Fibrous Dysplasia of Bone Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibrous Dysplasia of Bone from the curated CTD Gene-Disease Associations dataset.

Metaphyseal Dysplasia without Hypotrichosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Metaphyseal Dysplasia without Hypotrichosis from the curated CTD Gene-Disease Associations dataset.

OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA Gene Set

From CTD Gene-Disease Associations

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

Boomerang dysplasia Gene Set

From CTD Gene-Disease Associations

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

Pelviscapular dysplasia Gene Set

From CTD Gene-Disease Associations

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

Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 from the curated CTD Gene-Disease Associations dataset.

GELEOPHYSIC DYSPLASIA 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GELEOPHYSIC DYSPLASIA 1 from the curated CTD Gene-Disease Associations dataset.

Torticollis keloids cryptorchidism renal dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Torticollis keloids cryptorchidism renal dysplasia from the curated CTD Gene-Disease Associations dataset.

Campomelic Dysplasia Gene Set

From CTD Gene-Disease Associations

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

Alveolar capillary dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alveolar capillary dysplasia from the curated CTD Gene-Disease Associations dataset.

Ischiopatellar dysplasia Gene Set

From CTD Gene-Disease Associations

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

Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 from the curated CTD Gene-Disease Associations dataset.

ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE from the curated CTD Gene-Disease Associations dataset.

Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

Renal hepatic pancreatic dysplasia Dandy Walker cyst Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal hepatic pancreatic dysplasia Dandy Walker cyst from the curated CTD Gene-Disease Associations dataset.

Ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal dysplasia, ectrodactyly, and macular dystrophy 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.

ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.

DENTIN DYSPLASIA, TYPE II Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DENTIN DYSPLASIA, TYPE II from the curated CTD Gene-Disease Associations dataset.

Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondyloepimetaphyseal Dysplasia, Matrilin-3 Related from the curated CTD Gene-Disease Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 from the curated CTD Gene-Disease Associations dataset.

Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type from the curated CTD Gene-Disease Associations dataset.

Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies from the curated CTD Gene-Disease Associations dataset.

Mandibuloacral dysplasia with type A lipodystrophy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mandibuloacral dysplasia with type A lipodystrophy from the curated CTD Gene-Disease Associations dataset.

Oculodentodigital Dysplasia, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Oculodentodigital Dysplasia, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Spondyloepimetaphyseal Dysplasia, Missouri Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondyloepimetaphyseal Dysplasia, Missouri Type 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.

Acromesomelic dysplasia, Maroteaux type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Acromesomelic dysplasia, Maroteaux type from the curated CTD Gene-Disease Associations dataset.

Ectodermal Dysplasia 1, Anhidrotic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal Dysplasia 1, Anhidrotic from the curated CTD Gene-Disease Associations dataset.

ACROPECTOROVERTEBRAL DYSPLASIA Gene Set

From CTD Gene-Disease Associations

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

Spondyloepiphyseal dysplasia, congenita Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondyloepiphyseal dysplasia, congenita from the curated CTD Gene-Disease Associations dataset.

Spondyloepimetaphyseal Dysplasia, Pakistani Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondyloepimetaphyseal Dysplasia, Pakistani Type from the curated CTD Gene-Disease Associations dataset.

Spondyloepimetaphyseal Dysplasia, Aggrecan Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondyloepimetaphyseal Dysplasia, Aggrecan Type from the curated CTD Gene-Disease Associations dataset.

Parietal Foramina With Cleidocranial Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parietal Foramina With Cleidocranial Dysplasia from the curated CTD Gene-Disease Associations dataset.

Eiken Skeletal Dysplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Eiken Skeletal Dysplasia from the curated CTD Gene-Disease Associations dataset.

Kniest dysplasia Gene Set

From CTD Gene-Disease Associations

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

SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY from the curated CTD Gene-Disease Associations dataset.

Frontonasal dysplasia Gene Set

From CTD Gene-Disease Associations

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

Ectodermal dysplasia, hypohidrotic, with immune deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal dysplasia, hypohidrotic, with immune deficiency from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 1 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 3 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 2 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 5 from the curated CTD Gene-Disease Associations dataset.

Epiphyseal dysplasia, multiple, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epiphyseal dysplasia, multiple, 4 from the curated CTD Gene-Disease Associations dataset.

Hip Dysplasia, Beukes Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hip Dysplasia, Beukes Type from the curated CTD Gene-Disease Associations dataset.

craniometaphyseal dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

spondyloepimetaphyseal dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

thanatophoric dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

campomelic dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

otospondylomegaepiphyseal dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

kniest dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

sost-related sclerosing bone dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease sost-related sclerosing bone dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

boomerang dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

cleidocranial dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

spondyloepiphyseal dysplasia congenita Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease spondyloepiphyseal dysplasia congenita from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

spondyloepimetaphyseal dysplasia, strudwick type Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease spondyloepimetaphyseal dysplasia, strudwick type from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

diastrophic dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

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

hypohidrotic ectodermal dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease hypohidrotic ectodermal dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

multiple epiphyseal dysplasia Gene Set

From DISEASES Curated Gene-Disease Association Evidence Scores

genes involed in the disease multiple epiphyseal dysplasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

thanatophoric dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

metaphyseal dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

spondyloepimetaphyseal dysplasia, strudwick type Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease spondyloepimetaphyseal dysplasia, strudwick type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

dentin dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

spondyloepimetaphyseal dysplasia, missouri type Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease spondyloepimetaphyseal dysplasia, missouri type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spondyloepiphyseal dysplasia congenita Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

spondyloepimetaphyseal dysplasia, sponastrime type Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease spondyloepimetaphyseal dysplasia, sponastrime type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

multiple epiphyseal dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

acromesomelic dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

anauxetic dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

craniometaphyseal dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

sost-related sclerosing bone dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease sost-related sclerosing bone dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cleidocranial dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

benign mammary dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

acromesomelic dysplasia, maroteaux type Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

genes co-occuring with the disease acromesomelic dysplasia, maroteaux type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

schneckenbecken dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

otospondylomegaepiphyseal dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

craniodiaphyseal dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

diastrophic dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

thymic dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

hypohidrotic ectodermal dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

campomelic dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

spondyloepimetaphyseal dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

kniest dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

boomerang dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

acrocapitofemoral dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

fibrous dysplasia Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores

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

achondroplasia; musculoskeletal abnormalities; osteochondrodysplasias; thanatophoric dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease achondroplasia; musculoskeletal abnormalities; osteochondrodysplasias; thanatophoric dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple epiphyseal dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple epiphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia; infant, newborn, diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchopulmonary dysplasia; infant, newborn, diseases 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.

thanatophoric dysplasia Gene Set

From GAD Gene-Disease Associations

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

arrhythmogenic right ventricular dysplasia; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intestinal neuronal dysplasia type b (ind b) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease intestinal neuronal dysplasia type b (ind b) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia Gene Set

From GAD Gene-Disease Associations

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

bronchopulmonary dysplasia; respiratory distress syndrome, neonatal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchopulmonary dysplasia; respiratory distress syndrome, neonatal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; tachycardia, ventricular Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; tachycardia, ventricular in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia; respiratory distress syndrome, newborn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchopulmonary dysplasia; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; heart failure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; heart failure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple epiphyseal dysplasia; pseudoachondroplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple epiphyseal dysplasia; pseudoachondroplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular cardiomyopathy/dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular cardiomyopathy/dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ectodermal dysplasia; esophageal neoplasms; neoplasms, squamous cell; oesophageal neoplasm Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ectodermal dysplasia; esophageal neoplasms; neoplasms, squamous cell; oesophageal neoplasm in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; cardiomyopathies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; cardiomyopathies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; syncope Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; syncope in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

isolated congenital pituitary hypoplasia and septo-optic dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease isolated congenital pituitary hypoplasia and septo-optic dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone neoplasms; fibrous dysplasia, polyostotic; ossification, heterotopic; osteoma; pseudohypoparathyroidism; skin neoplasms; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spondyloepiphyseal dysplasia tall stature and precocious osteoarthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spondyloepiphyseal dysplasia tall stature and precocious osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoarthritis; hip dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoarthritis; hip dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fibrous dysplasia of bone; osteitis fibrosa disseminata; osteosarcoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fibrous dysplasia of bone; osteitis fibrosa disseminata; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

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

pseudoachondroplasia and multiple epiphyseal dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pseudoachondroplasia and multiple epiphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

strudwick variant of spondyloepimetaphyseal dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease strudwick variant of spondyloepimetaphyseal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

multiple oesophageal dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple oesophageal dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

risk of cervical dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease risk of cervical dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia; death, sudden, cardiac; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hpv-associated cervical dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hpv-associated cervical dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia; chorioamnionitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchopulmonary dysplasia; chorioamnionitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmogenic right ventricular dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autosomal dominant anhidrotic ectodermal dysplasia and t cell immunodeficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autosomal dominant anhidrotic ectodermal dysplasia and t cell immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleidocranial dysplasia Gene Set

From GAD Gene-Disease Associations

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

familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease familial spondyloepiphyseal dysplasia tarda, brachydactyly, and precocious osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia. Gene Set

From GAD Gene-Disease Associations

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

bronchopulmonary dysplasia; Gene Set

From GAD Gene-Disease Associations

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

arrhythmias, cardiac; arrhythmogenic right ventricular dysplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arrhythmias, cardiac; arrhythmogenic right ventricular dysplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cleft lip; cleft palate; ectodermal dysplasia; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip; cleft palate; ectodermal dysplasia; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fibrous dysplasia Gene Set

From GAD Gene-Disease Associations

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

dysplasia Gene Set

From GeneRIF Biological Term Annotations

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

Bronchopulmonary dysplasia Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

nail dysplasia Gene Set

From HPO Gene-Disease Associations

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

retinal dysplasia Gene Set

From HPO Gene-Disease Associations

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

multiple epiphyseal dysplasia Gene Set

From HPO Gene-Disease Associations

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

acetabular dysplasia Gene Set

From HPO Gene-Disease Associations

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

skeletal dysplasia Gene Set

From HPO Gene-Disease Associations

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

hip dysplasia Gene Set

From HPO Gene-Disease Associations

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

chorioretinal dysplasia Gene Set

From HPO Gene-Disease Associations

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

metaphyseal dysplasia Gene Set

From HPO Gene-Disease Associations

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

spondyloepimetaphyseal dysplasia Gene Set

From HPO Gene-Disease Associations

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

fibrous dysplasia of the bones Gene Set

From HPO Gene-Disease Associations

genes associated with the fibrous dysplasia of the bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

frontoparietal cortical dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the frontoparietal cortical dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lethal skeletal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the lethal skeletal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cortical dysplasia Gene Set

From HPO Gene-Disease Associations

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

brainstem dysplasia Gene Set

From HPO Gene-Disease Associations

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

spondylometaphyseal dysplasia Gene Set

From HPO Gene-Disease Associations

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

polyostotic fibrous dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the polyostotic fibrous dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cystic renal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the cystic renal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fingernail dysplasia Gene Set

From HPO Gene-Disease Associations

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

epiphyseal dysplasia Gene Set

From HPO Gene-Disease Associations

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

ectodermal dysplasia Gene Set

From HPO Gene-Disease Associations

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

spondyloepiphyseal dysplasia Gene Set

From HPO Gene-Disease Associations

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

optic nerve dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the optic nerve dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multicystic kidney dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the multicystic kidney dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

hypohidrotic ectodermal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the hypohidrotic ectodermal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

polycystic kidney dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the polycystic kidney dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar dysplasia Gene Set

From HPO Gene-Disease Associations

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

hair-nail ectodermal dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the hair-nail ectodermal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

toenail dysplasia Gene Set

From HPO Gene-Disease Associations

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

renal dysplasia Gene Set

From HPO Gene-Disease Associations

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

diaphyseal dysplasia Gene Set

From HPO Gene-Disease Associations

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

septo-optic dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the septo-optic dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dysplasia of the femoral head Gene Set

From HPO Gene-Disease Associations

genes associated with the dysplasia of the femoral head phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Septo-Optic Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Septo-Optic Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Bronchopulmonary Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Ectodermal Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Thanatophoric Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Fibromuscular Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Fibrous Dysplasia, Polyostotic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Fibrous Dysplasia, Polyostotic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Fibrous Dysplasia of Bone Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Fibrous Dysplasia of Bone phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Cleidocranial Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Uterine Cervical Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Uterine Cervical Dysplasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Arrhythmogenic Right Ventricular Dysplasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Adrenocortical dysplasia protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Adrenocortical dysplasia protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

?corneal intraepithelial dyskeratosis and ectodermal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?corneal intraepithelial dyskeratosis and ectodermal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

?epiphyseal dysplasia, multiple, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?epiphyseal dysplasia, multiple, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloperipheral dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloperipheral dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 10 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

acampomelic campomelic dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the acampomelic campomelic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal, dysplasia, anhidrotic, lymphedema and immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

frontometaphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the frontometaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

campomelic dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the campomelic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

metaphyseal dysplasia without hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the metaphyseal dysplasia without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 4 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 4 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

developmental dysplasia of the hip 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the developmental dysplasia of the hip 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

smith-mccort dysplasia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the smith-mccort dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

parietal foramina with cleidocranial dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the parietal foramina with cleidocranial dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

craniometaphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniometaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

renal-hepatic-pancreatic dysplasia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal-hepatic-pancreatic dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 6, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 6, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia/short stature syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia/short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 6 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 6 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

craniofacial-skeletal-dermatologic dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniofacial-skeletal-dermatologic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

focal cortical dysplasia, taylor balloon cell type Gene Set

From OMIM Gene-Disease Associations

genes associated with the focal cortical dysplasia, taylor balloon cell type phenotype from the curated OMIM Gene-Disease Associations dataset.

thanatophoric dysplasia, type i Gene Set

From OMIM Gene-Disease Associations

genes associated with the thanatophoric dysplasia, type i phenotype from the curated OMIM Gene-Disease Associations dataset.

mandibuloacral dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the mandibuloacral dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia, ectrodactyly, and macular dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia, ectrodactyly, and macular dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

diastrophic dysplasia, broad bone-platyspondylic variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the diastrophic dysplasia, broad bone-platyspondylic variant phenotype from the curated OMIM Gene-Disease Associations dataset.

cleft lip/palate-ectodermal dysplasia syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the cleft lip/palate-ectodermal dysplasia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

otospondylomegaepiphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the otospondylomegaepiphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

boomerang dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the boomerang dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

frontonasal dysplasia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the frontonasal dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

frontonasal dysplasia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the frontonasal dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

craniolenticulosutural dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniolenticulosutural dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cranioectodermal dysplasia 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cranioectodermal dysplasia 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

cranioectodermal dysplasia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cranioectodermal dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cranioectodermal dysplasia 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cranioectodermal dysplasia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cranioectodermal dysplasia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cranioectodermal dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 7 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 7 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 3, witkop type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 3, witkop type phenotype from the curated OMIM Gene-Disease Associations dataset.

spondylometaepiphyseal dysplasia, short limb-hand type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondylometaepiphyseal dysplasia, short limb-hand type phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 7, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 7, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

oculodentodigital dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the oculodentodigital dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia, anhidrotic, with t-cell immunodeficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia, anhidrotic, with t-cell immunodeficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

greenberg skeletal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the greenberg skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

acromesomelic dysplasia, maroteaux type Gene Set

From OMIM Gene-Disease Associations

genes associated with the acromesomelic dysplasia, maroteaux type phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 11 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 5, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 5, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

smith-mccort dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the smith-mccort dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

craniodiaphyseal dysplasia, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniodiaphyseal dysplasia, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, with myopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, with myopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

septooptic dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the septooptic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

acromesomelic dysplasia, hunter-thompson type Gene Set

From OMIM Gene-Disease Associations

genes associated with the acromesomelic dysplasia, hunter-thompson type phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepimetaphyseal dysplasia, missouri type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepimetaphyseal dysplasia, missouri type phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

macrocephaly with multiple epiphyseal dysplasia and distinctive facies Gene Set

From OMIM Gene-Disease Associations

genes associated with the macrocephaly with multiple epiphyseal dysplasia and distinctive facies phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepiphyseal dysplasia tarda Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepiphyseal dysplasia tarda phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune polyendocrinopathy syndrome , type i, with or without reversible metaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepimetaphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepimetaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 1, hypohidrotic, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 1, hypohidrotic, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

diastrophic dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the diastrophic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

platyspondylic skeletal dysplasia, torrance type Gene Set

From OMIM Gene-Disease Associations

genes associated with the platyspondylic skeletal dysplasia, torrance type phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia-syndactyly syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia-syndactyly syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

schneckenbecken dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the schneckenbecken dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

dentin dysplasia, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the dentin dysplasia, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

de la chapelle dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the de la chapelle dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

cortical dysplasia-focal epilepsy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the cortical dysplasia-focal epilepsy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

craniometaphyseal dysplasia, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniometaphyseal dysplasia, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 4, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 4, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

alveolar capillary dysplasia with misalignment of pulmonary veins Gene Set

From OMIM Gene-Disease Associations

genes associated with the alveolar capillary dysplasia with misalignment of pulmonary veins phenotype from the curated OMIM Gene-Disease Associations dataset.

kniest dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the kniest dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

otodental dysplasia chromsome deletion syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the otodental dysplasia chromsome deletion syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, with myopia and deafness Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, with myopia and deafness phenotype from the curated OMIM Gene-Disease Associations dataset.

acrocapitofemoral dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the acrocapitofemoral dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

spondylometaphyseal dysplasia with cone-rod dystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondylometaphyseal dysplasia with cone-rod dystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepiphyseal dysplasia tarda with progressive arthropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepiphyseal dysplasia tarda with progressive arthropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

craniofrontonasal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniofrontonasal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

{renal dysplasia, cystic, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {renal dysplasia, cystic, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

langer mesomelic dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the langer mesomelic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

vitreoretinopathy with phalangeal epiphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the vitreoretinopathy with phalangeal epiphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

bent bone dysplasia syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the bent bone dysplasia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

acromicric dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the acromicric dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 9 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 9 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

acropectorovertebral dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the acropectorovertebral dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

dentin dysplasia, type i, with microdontia and misshapen teeth Gene Set

From OMIM Gene-Disease Associations

genes associated with the dentin dysplasia, type i, with microdontia and misshapen teeth phenotype from the curated OMIM Gene-Disease Associations dataset.

?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

spondylometaphyseal dysplasia, kozlowski type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondylometaphyseal dysplasia, kozlowski type phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypoparathyroidism, sensorineural deafness, and renal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypoparathyroidism, sensorineural deafness, and renal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation-skeletal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation-skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

desbuquois dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the desbuquois dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

spondylo-megaepiphyseal-metaphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondylo-megaepiphyseal-metaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

anauxetic dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the anauxetic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 3 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 9, hair/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 9, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

cleidocranial dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the cleidocranial dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia/skin fragility syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia/skin fragility syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

gnathodiaphyseal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the gnathodiaphyseal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

focal facial dermal dysplasia 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the focal facial dermal dysplasia 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepimetaphyseal dysplasia with joint laxity, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepimetaphyseal dysplasia with joint laxity, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 8, hair/tooth/nail type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 8, hair/tooth/nail type phenotype from the curated OMIM Gene-Disease Associations dataset.

schimke immunoosseous dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the schimke immunoosseous dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia, hypohidrotic, with immune deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia, hypohidrotic, with immune deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 8 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 8 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia-syndactyly syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia-syndactyly syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia, familial, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia, familial, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

mandibuloacral dysplasia with type b lipodystrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the mandibuloacral dysplasia with type b lipodystrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

terminal osseous dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the terminal osseous dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

desbuquois dysplasia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the desbuquois dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

?frontonasal dysplasia 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?frontonasal dysplasia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

epiphyseal dysplasia, multiple, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the epiphyseal dysplasia, multiple, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

cardiac valvular dysplasia, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the cardiac valvular dysplasia, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

campomelic dysplasia with autosomal sex reversal Gene Set

From OMIM Gene-Disease Associations

genes associated with the campomelic dysplasia with autosomal sex reversal phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

geleophysic dysplasia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the geleophysic dysplasia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

geleophysic dysplasia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the geleophysic dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

dyssegmental dysplasia, silverman-handmaker type Gene Set

From OMIM Gene-Disease Associations

genes associated with the dyssegmental dysplasia, silverman-handmaker type phenotype from the curated OMIM Gene-Disease Associations dataset.

gracile bone dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the gracile bone dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 2 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 2 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

odontoonychodermal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the odontoonychodermal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

hip dysplasia, beukes type Gene Set

From OMIM Gene-Disease Associations

genes associated with the hip dysplasia, beukes type phenotype from the curated OMIM Gene-Disease Associations dataset.

cleidocranial dysplasia, forme fruste, with brachydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the cleidocranial dysplasia, forme fruste, with brachydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

cortical dysplasia, complex, with other brain malformations 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cortical dysplasia, complex, with other brain malformations 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cortical dysplasia, complex, with other brain malformations 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cortical dysplasia, complex, with other brain malformations 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

cortical dysplasia, complex, with other brain malformations 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cortical dysplasia, complex, with other brain malformations 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

cortical dysplasia, complex, with other brain malformations 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cortical dysplasia, complex, with other brain malformations 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

cortical dysplasia, complex, with other brain malformations 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cortical dysplasia, complex, with other brain malformations 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

cortical dysplasia, complex, with other brain malformations 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cortical dysplasia, complex, with other brain malformations 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair Gene Set

From OMIM Gene-Disease Associations

genes associated with the arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair phenotype from the curated OMIM Gene-Disease Associations dataset.

focal facial dermal dysplasia 3, setleis type Gene Set

From OMIM Gene-Disease Associations

genes associated with the focal facial dermal dysplasia 3, setleis type phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 5 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 5 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

czech dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the czech dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepimetaphyseal dysplasia, aggrecan type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepimetaphyseal dysplasia, aggrecan type phenotype from the curated OMIM Gene-Disease Associations dataset.

oculodentodigital dysplasia, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the oculodentodigital dysplasia, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

mesomelic dysplasia, kantaputra type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mesomelic dysplasia, kantaputra type phenotype from the curated OMIM Gene-Disease Associations dataset.

cleidocranial dysplasia, forme fruste, dental anomalies only Gene Set

From OMIM Gene-Disease Associations

genes associated with the cleidocranial dysplasia, forme fruste, dental anomalies only phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepiphyseal dysplasia, kimberley type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepiphyseal dysplasia, kimberley type phenotype from the curated OMIM Gene-Disease Associations dataset.

metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

metatropic dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the metatropic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

thanatophoric dysplasia, type ii Gene Set

From OMIM Gene-Disease Associations

genes associated with the thanatophoric dysplasia, type ii phenotype from the curated OMIM Gene-Disease Associations dataset.

?renal-hepatic-pancreatic dysplasia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?renal-hepatic-pancreatic dysplasia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

osteoglophonic dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteoglophonic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

spondyloepiphyseal dysplasia with congenital joint dislocations Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondyloepiphyseal dysplasia with congenital joint dislocations phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 2, clouston type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 2, clouston type phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD) Gene Set

From Reactome Pathways 2014

proteins participating in the Defective TBXAS1 causes Ghosal hematodiaphyseal dysplasia (GHDD) pathway from the Reactome Pathways dataset.

Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) Gene Set

From Reactome Pathways 2014

proteins participating in the Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) pathway from the Reactome Pathways dataset.

Defective SLC35D1 causes Schneckenbecken dysplasia (SCHBCKD) Gene Set

From Reactome Pathways 2014

proteins participating in the Defective SLC35D1 causes Schneckenbecken dysplasia (SCHBCKD) pathway from the Reactome Pathways dataset.

chronic ulcerative colitis (CUC), ulcerative colitis?associated dysplasia (UCD), colitis-associated cancer (CAC) Gene Set

From PhosphoSitePlus Phosphosite-Disease Associations

proteins associated with the disease chronic ulcerative colitis (CUC), ulcerative colitis?associated dysplasia (UCD), colitis-associated cancer (CAC) from the curated PhosphoSitePlus Phosphosite-Disease Associations dataset.

Congenital Dysplasia Of The Hip Gene Set

From DisGeNET Gene-Disease Associations

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

Nail Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Alveolar Capillary Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Bronchopulmonary Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Acute Myeloid Leukemia With Multilineage Dysplasia Following Myelodysplastic Syndrome Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Acute Myeloid Leukemia With Multilineage Dysplasia Following Myelodysplastic Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Pyle Metaphyseal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Skeletal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Ectodermal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Dysplasia Of Anus Gene Set

From DisGeNET Gene-Disease Associations

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

Multiple Epiphyseal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Spondyloepiphyseal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Polyostotic Fibrous Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Arrhythmogenic Right Ventricular Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Campomelic Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Craniometaphyseal Dysplasia, Autosomal Dominant Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Craniometaphyseal Dysplasia, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Diastrophic Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Mild Bronchopulmonary Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Neuronal Intestinal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Thanatophoric Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Thanatophoric Dysplasia, Type I (Disorder) Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Thanatophoric Dysplasia, Type I (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Fibrous Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Primary Pigmented Nodular Adrenal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Primary Pigmented Nodular Adrenal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Progressive Pseudorheumatoid Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Cervical Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Fibromuscular Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Smith-Mccort Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Dentin Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Lethal Skeletal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Bone Marrow Myeloid Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Bone Marrow Myeloid Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Acromicric Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Cleidocranial Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Geleophysic Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Craniofacial Fibrous Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Hip Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Cortical Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Esophageal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Mesomelic Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Focal Cortical Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Spondylometaphyseal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Mitral Valve Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Autoimmune Polyendocrinopathy Syndrome, Type I, With Reversible Metaphyseal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Autoimmune Polyendocrinopathy Syndrome, Type I, With Reversible Metaphyseal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Schimke Immunoosseous Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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

Focal Dysplasia Gene Set

From DisGeNET Gene-Disease Associations

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