Limited mobility of proximal interphalangeal joint

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Results for "Limited mobility of proximal interphalangeal joint": 192 genes, 611 gene sets

Name
HMGN2P31 Gene high mobility* group nucleosomal binding domain 2 pseudogene 31*
HMGB3P5 Gene high mobility* group box 3 pseudogene 5*
HMGN2P19 Gene high mobility* group nucleosomal binding domain 2 pseudogene 19*
HMGN2P18 Gene high mobility* group nucleosomal binding domain 2 pseudogene 18*
HMGN2P12 Gene high mobility* group nucleosomal binding domain 2 pseudogene 12*
HMGN2P11 Gene high mobility* group nucleosomal binding domain 2 pseudogene 11*
HMGN2P10 Gene high mobility* group nucleosomal binding domain 2 pseudogene10*
HMGN2P17 Gene high mobility* group nucleosomal binding domain 2 pseudogene 17*
HMGN2P16 Gene high mobility* group nucleosomal binding domain 2 pseudogene 16*
HMGN2P15 Gene high mobility* group nucleosomal binding domain 2 pseudogene 15*
HMGN2P14 Gene high mobility* group nucleosomal binding domain 2 pseudogene14*
HMGN1P9 Gene high mobility* group nucleosome binding domain 1 pseudogene*
HMGN1P4 Gene high mobility* group nucleosome binding domain 1 pseudogene 4*
HMGN1P5 Gene high mobility* group nucleosome binding domain 1 pseudogene 5*
HMGN1P6 Gene high mobility* group nucleosome binding domain 1 pseudogene 6*
HMGN1P7 Gene high mobility* group nucleosome binding domain 1 pseudogene 7*
HMGN1P1 Gene high mobility* group nucleosome binding domain 1 pseudogene 1*
HMGN1P2 Gene high mobility* group nucleosome binding domain 1 pseudogene 2*
LOC100129956 Gene high mobility* group nucleosomal binding domain 2 pseudogene*
HMGB3 Gene high mobility* group box 3* This gene encodes a member of a family of proteins containing one or more high mobility group DNA-binding motifs. The encoded protein plays an important role in maintaining stem cell populations, and may be aberrantly expressed in tumor cells. A mutation in this gene was associated with microphthalmia, syndromic 13. There are numerous pseudogenes of this gene on multiple chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]
HMGB4 Gene high mobility* group box 4* Predicted to enable DNA binding activity, bending. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleus. [provided by Alliance of Genome Resources, Mar 2025]
HMGN2P13 Gene high mobility* group nucleosomal binding domain 2 pseudogene 13*
HMGB1P12 Gene high mobility* group box 1 pseudogene 12*
HMGB1P10 Gene high mobility* group box 1 pseudogene 10*
HMGB1P16 Gene high mobility* group box 1 pseudogene 16*
HMGB1P17 Gene high mobility* group box 1 pseudogene 17*
HMGB1P36 Gene high mobility* group box 1 pseudogene 36*
HMGB3P22 Gene high mobility* group box 3 pseudogene 22*
HMGN1P8 Gene high mobility* group nucleosome binding domain 1 pseudogene 8*
HMGN1P3 Gene high mobility* group nucleosome binding domain 1 pseudogene 3*
HMGB1P1 Gene high mobility* group box 1 pseudogene 1* This gene may represent an evolving retropseudogene of the high-mobility group box 1 gene, which has multiple pseudogenes. This gene has an intact open reading frame, where the length of encoded protein is conserved, compared to the high-mobility group box 1 protein. However, due to the lack of conclusive evidence for specific transcription at this location, this locus is currently represented as a pseudogene. [provided by RefSeq, Jan 2010]
HMGB1P3 Gene high mobility* group box 1 pseudogene 3*
HMGB1P4 Gene high mobility* group box 1 pseudogene 4*
HMGB1P5 Gene high mobility* group box 1 pseudogene 5*
HMGN1P16 Gene high mobility* group nucleosome binding domain 1 pseudogene 16*
HMGN1P17 Gene high mobility* group nucleosome binding domain 1 pseudogene 17*
HMGN1P13 Gene high mobility* group nucleosome binding domain 1 pseudogene 13*
HMGN1P10 Gene high mobility* group nucleosome binding domain 1 pseudogene 10*
HMGN1P11 Gene high mobility* group nucleosome binding domain 1 pseudogene 11*
HMGN1P33 Gene high mobility* group nucleosome binding domain 1 pseudogene 33*
HMGN1P34 Gene high mobility* group nucleosome binding domain 1 pseudogene 34*
HMGB3P32 Gene high mobility* group box 3 pseudogene 32*
HMGB3P30 Gene high mobility* group box 3 pseudogene 30*
HMGB3P31 Gene high mobility* group box 3 pseudogene 31*
HMGN2P33 Gene high mobility* group nucleosomal binding domain 2 pseudogene 33*
HMGN2P32 Gene high mobility* group nucleosomal binding domain 2 pseudogene 32*
HMGN2P35 Gene high mobility* group nucleosomal binding domain 2 pseudogene 35*
HMGN2P34 Gene high mobility* group nucleosomal binding domain 2 pseudogene 34*
HMGN2P37 Gene high mobility* group nucleosomal binding domain 2 pseudogene 37*
HMGN2P36 Gene high mobility* group nucleosomal binding domain 2 pseudogene 36*
HMGN2P39 Gene high mobility* group nucleosomal binding domain 2 pseudogene 39*
HMGN2P38 Gene high mobility* group nucleosomal binding domain 2 pseudogene 38*
HMGB1P27 Gene high mobility* group box 1 pseudogene 27*
HMGB1P24 Gene high mobility* group box 1 pseudogene 24*
HMGB1P22 Gene high mobility* group box 1 pseudogene 22*
HMGB1P29 Gene high mobility* group box 1 pseudogene 29*
HMGB1P18 Gene high mobility* group box 1 pseudogene 18*
HMGB1P19 Gene high mobility* group box 1 pseudogene 19*
HMGB1P11 Gene high mobility* group box 1 pseudogene 11*
HMGB1P14 Gene high mobility* group box 1 pseudogene 14*
HMGB1P15 Gene high mobility* group box 1 pseudogene 15*
HMGB2 Gene high mobility* group box 2* This gene encodes a member of the non-histone chromosomal high mobility group protein family. The proteins of this family are chromatin-associated and ubiquitously distributed in the nucleus of higher eukaryotic cells. In vitro studies have demonstrated that this protein is able to efficiently bend DNA and form DNA circles. These studies suggest a role in facilitating cooperative interactions between cis-acting proteins by promoting DNA flexibility. This protein was also reported to be involved in the final ligation step in DNA end-joining processes of DNA double-strand breaks repair and V(D)J recombination. [provided by RefSeq, Jul 2008]
HMGB1 Gene high mobility* group box 1* This gene encodes a protein that belongs to the High Mobility Group-box superfamily. The encoded non-histone, nuclear DNA-binding protein regulates transcription, and is involved in organization of DNA. This protein plays a role in several cellular processes, including inflammation, cell differentiation and tumor cell migration. Multiple pseudogenes of this gene have been identified. Alternative splicing results in multiple transcript variants that encode the same protein. [provided by RefSeq, Sep 2015]
HMGN3P1 Gene high mobility* group nucleosomal binding domain 3 pseudogene 1*
HMGB1P45 Gene high mobility* group box 1 pseudogene 45*
HMGA2 Gene high mobility* group AT-hook 2* This gene encodes a protein that belongs to the non-histone chromosomal high mobility group (HMG) protein family. HMG proteins function as architectural factors and are essential components of the enhancesome. This protein contains structural DNA-binding domains and may act as a transcriptional regulating factor. Identification of the deletion, amplification, and rearrangement of this gene that are associated with myxoid liposarcoma suggests a role in adipogenesis and mesenchymal differentiation. A gene knock out study of the mouse counterpart demonstrated that this gene is involved in diet-induced obesity. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]
HMGB1P41 Gene high mobility* group box 1 pseudogene 41*
HMGB1P40 Gene high mobility* group box 1 pseudogene 40*
HMGB1P44 Gene high mobility* group box 1 pseudogene 44*
HMGB1P47 Gene high mobility* group box 1 pseudogene 47*
HMGB1P49 Gene high mobility* group box 1 pseudogene 49*
HMGB1P48 Gene high mobility* group box 1 pseudogene 48*
HMGN1P23 Gene high mobility* group nucleosome binding domain 1 pseudogene 23*
HMGN1P22 Gene high mobility* group nucleosome binding domain 1 pseudogene 22*
HMGN1P21 Gene high mobility* group nucleosome binding domain 1 pseudogene 21*
HMGN1P27 Gene high mobility* group nucleosome binding domain 1 pseudogene 27*
HMGN1P26 Gene high mobility* group nucleosome binding domain 1 pseudogene 26*
HMGN1P25 Gene high mobility* group nucleosome binding domain 1 pseudogene 25*
HMGN1P24 Gene high mobility* group nucleosome binding domain 1 pseudogene 24*
HMGN1P29 Gene high mobility* group nucleosome binding domain 1 pseudogene 29*
HMGN1P28 Gene high mobility* group nucleosome binding domain 1 pseudogene 28*
HMGB3P2 Gene high mobility* group box 3 pseudogene 2*
HMGB3P3 Gene high mobility* group box 3 pseudogene 3*
HMGB3P1 Gene high mobility* group box 3 pseudogene 1*
HMGB3P6 Gene high mobility* group box 3 pseudogene 6*
HMGB3P7 Gene high mobility* group box 3 pseudogene 7*
HMGB3P4 Gene high mobility* group box 3 pseudogene 4*
HMGB3P8 Gene high mobility* group box 3 pseudogene 8*
HMGB3P9 Gene high mobility* group box 3 pseudogene 9*
HMG20A Gene high mobility* group 20A* Enables identical protein binding activity. Predicted to be involved in regulation of gene expression. Predicted to act upstream of or within negative regulation of neuron differentiation; negative regulation of protein sumoylation; and negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025]
HMG20B Gene high mobility* group 20B* Predicted to enable DNA binding activity. Predicted to be involved in regulation of gene expression. Predicted to act upstream of or within negative regulation of protein sumoylation; positive regulation of neuron differentiation; and skeletal muscle cell differentiation. Located in nuclear body. [provided by Alliance of Genome Resources, Mar 2025]
HMGA1P4 Gene high mobility* group AT-hook 1 pseudogene 4*
HMGA1P6 Gene high mobility* group AT-hook 1 pseudogene 6*
HMGB1P34 Gene high mobility* group box 1 pseudogene 34*
HMGB1P37 Gene high mobility* group box 1 pseudogene 37*
HMGB1P30 Gene high mobility* group box 1 pseudogene 30*
HMGB1P38 Gene high mobility* group box 1 pseudogene 38*
HMGB1P39 Gene high mobility* group box 1 pseudogene 39*
HMGN1P35 Gene high mobility* group nucleosome binding domain 1 pseudogene 35*
HMGB1P35 Gene high mobility* group box 1 pseudogene 35*
HMGB1P31 Gene high mobility* group box 1 pseudogene 31*
HMGB1P32 Gene high mobility* group box 1 pseudogene 32*
HMGN5 Gene high mobility* group nucleosome binding domain 5* This gene encodes a nuclear protein with similarities to the high mobility group proteins, HMG14 and HMG17, which suggests that this protein may function as a nucleosomal binding and transcriptional activating protein. [provided by RefSeq, Sep 2009]
HMGN4 Gene high mobility* group nucleosomal binding domain 4* The protein encoded by this gene, a member of the HMGN protein family, is thought to reduce the compactness of the chromatin fiber in nucleosomes, thereby enhancing transcription from chromatin templates. [provided by RefSeq, Mar 2013]
HMGN3 Gene high mobility* group nucleosomal binding domain 3* The protein encoded by this gene binds thyroid hormone receptor beta in the presence of thyroid hormone. The encoded protein, a member of the HMGN protein family, is thought to reduce the compactness of the chromatin fiber in nucleosomes, thereby enhancing transcription from chromatin templates. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. There is a related pseudogene on chromosome 1. [provided by RefSeq, Jan 2016]
HMGN2 Gene high mobility* group nucleosomal binding domain 2* The protein encoded by this gene binds nucleosomal DNA and is associated with transcriptionally active chromatin. Along with a similar protein, HMGN1, the encoded protein may help maintain an open chromatin configuration around transcribable genes. The protein has also been found to have antimicrobial activity against bacteria, viruses and fungi. [provided by RefSeq, Oct 2014]
HMGN1 Gene high mobility* group nucleosome binding domain 1* The protein encoded by this gene binds nucleosomal DNA and is associated with transcriptionally active chromatin. Along with a similar protein, HMG17, the encoded protein may help maintain an open chromatin configuration around transcribable genes. [provided by RefSeq, Aug 2011]
HMGA1P8 Gene high mobility* group AT-hook 1 pseudogene 8 (functional)*
HMGA1P5 Gene high mobility* group AT-hook 1 pseudogene 5*
HMGA1P7 Gene high mobility* group AT-hook 1 pseudogene 7*
HMGA1P1 Gene high mobility* group AT-hook 1 pseudogene 1*
HMGA1P3 Gene high mobility* group AT-hook 1 pseudogene 3*
HMGA1P2 Gene high mobility* group AT-hook 1 pseudogene 2*
HMGB1P33 Gene high mobility* group box 1 pseudogene 33*
HMGA1 Gene high mobility* group AT-hook 1* This gene encodes a chromatin-associated protein involved in the regulation of gene transcription, integration of retroviruses into chromosomes, and the metastatic progression of cancer cells. The encoded protein preferentially binds to the minor groove of AT-rich regions in double-stranded DNA. Multiple transcript variants encoding different isoforms have been found for this gene. Pseudogenes of this gene have been identified on multiple chromosomes. [provided by RefSeq, Jan 2016]
HMGN2P30 Gene high mobility* group nucleosomal binding domain 2 pseudogene 30*
HMGN2P26 Gene high mobility* group nucleosomal binding domain 2 pseudogene 26*
HMGN2P27 Gene high mobility* group nucleosomal binding domain 2 pseudogene 27*
HMGN2P22 Gene high mobility* group nucleosomal binding domain 2 pseudogene 22*
HMGN2P23 Gene high mobility* group nucleosomal binding domain 2 pseudogene 23*
HMGN2P20 Gene high mobility* group nucleosomal binding domain 2 pseudogene 20*
HMGN2P21 Gene high mobility* group nucleosomal binding domain 2 pseudogene 21*
HMGN2P7 Gene high mobility* group nucleosomal binding domain 2 pseudogene 7*
HMGN2P6 Gene high mobility* group nucleosomal binding domain 2 pseudogene 6*
HMGN2P5 Gene high mobility* group nucleosomal binding domain 2 pseudogene 5*
HMGN2P3 Gene high mobility* group nucleosomal binding domain 2 pseudogene 3*
HMGN2P2 Gene high mobility* group nucleosomal binding domain 2 pseudogene 2*
HMGN2P1 Gene high mobility* group nucleosomal binding domain 2 pseudogene 1*
HMGN2P9 Gene high mobility* group nucleosomal binding domain 2 pseudogene 9*
HMGB1P26 Gene high mobility* group box 1 pseudogene 26*
HMGB1P23 Gene high mobility* group box 1 pseudogene 23*
HMGB1P28 Gene high mobility* group box 1 pseudogene 28*
HMGB1P8 Gene high mobility* group box 1 pseudogene 8*
HMGB1P9 Gene high mobility* group box 1 pseudogene 9*
HMGN1P14 Gene high mobility* group nucleosome binding domain 1 pseudogene 14*
HMGN1P15 Gene high mobility* group nucleosome binding domain 1 pseudogene 15*
HMGN1P19 Gene high mobility* group nucleosome binding domain 1 pseudogene 19*
HMGB1P25 Gene high mobility* group box 1 pseudogene 25*
HMGB1P21 Gene high mobility* group box 1 pseudogene 21*
HMGB1P20 Gene high mobility* group box 1 pseudogene 20*
HMGB1P43 Gene high mobility* group box 1 pseudogene 43*
HMGB1P42 Gene high mobility* group box 1 pseudogene 42*
HMGB1P46 Gene high mobility* group box 1 pseudogene 46*
HMGB2P1 Gene high mobility* group box 2 pseudogene 1*
HMGN1P18 Gene high mobility* group nucleosome binding domain 1 pseudogene 18*
HMGB1P13 Gene high mobility* group box 1 pseudogene 13*
HMGB3P25 Gene high mobility* group box 3 pseudogene 25*
HMGB3P24 Gene high mobility* group box 3 pseudogene 24*
HMGB3P27 Gene high mobility* group box 3 pseudogene 27*
HMGB3P26 Gene high mobility* group box 3 pseudogene 26*
HMGB3P20 Gene high mobility* group box 3 pseudogene 20*
HMGN2P28 Gene high mobility* group nucleosomal binding domain 2 pseudogene 28*
HMGN2P29 Gene high mobility* group nucleosomal binding domain 2 pseudogene 29*
HMGN2P25 Gene high mobility* group nucleosomal binding domain 2 pseudogene 25*
HMGN2P24 Gene high mobility* group nucleosomal binding domain 2 pseudogene 24*
HMGN1P30 Gene high mobility* group nucleosome binding domain 1 pseudogene 30*
HMGN1P31 Gene high mobility* group nucleosome binding domain 1 pseudogene 31*
HMGN1P32 Gene high mobility* group nucleosome binding domain 1 pseudogene 32*
HMGN1P36 Gene high mobility* group nucleosome binding domain 1 pseudogene 36*
HMGN1P37 Gene high mobility* group nucleosome binding domain 1 pseudogene 37*
HMGN1P38 Gene high mobility* group nucleosome binding domain 1 pseudogene 38*
TOX Gene thymocyte selection-associated high mobility* group box* The protein encoded by this gene contains a HMG box DNA binding domain. HMG boxes are found in many eukaryotic proteins involved in chromatin assembly, transcription and replication. This protein may function to regulate T-cell development.[provided by RefSeq, Apr 2009]
HMGB1P6 Gene high mobility* group box 1 pseudogene 6*
HMGB1P7 Gene high mobility* group box 1 pseudogene 7*
HMGN2P44 Gene high mobility* group nucleosomal binding domain 2 pseudogene 44*
HMGN2P45 Gene high mobility* group nucleosomal binding domain 2 pseudogene 45*
HMGN2P46 Gene high mobility* group nucleosomal binding domain 2 pseudogene 46* Predicted to enable chromatin binding activity. Predicted to be involved in chromatin organization. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025]
HMGN2P40 Gene high mobility* group nucleosomal binding domain 2 pseudogene 40*
HMGN2P41 Gene high mobility* group nucleosomal binding domain 2 pseudogene 41*
HMGN2P42 Gene high mobility* group nucleosomal binding domain 2 pseudogene 42*
HMGN2P43 Gene high mobility* group nucleosomal binding domain 2 pseudogene 43*
TOX4 Gene TOX high mobility* group box family member 4* Predicted to enable chromatin DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in chromatin and chromosome, telomeric region. Part of PTW/PP1 phosphatase complex. [provided by Alliance of Genome Resources, Mar 2025]
TOX3 Gene TOX high mobility* group box family member 3* The protein encoded by this gene contains an HMG-box, indicating that it may be involved in bending and unwinding of DNA and alteration of chromatin structure. The C-terminus of the encoded protein is glutamine-rich due to CAG repeats in the coding sequence. A minor allele of this gene has been implicated in an elevated risk of breast cancer. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2009]
TOX2 Gene TOX high mobility* group box family member 2* Enables transcription coactivator activity. Involved in positive regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Mar 2025]
HMGN1P20 Gene high mobility* group nucleosome binding domain 1 pseudogene 20*
HMGB3P14 Gene high mobility* group box 3 pseudogene 14*
HMGB3P15 Gene high mobility* group box 3 pseudogene 15*
HMGB3P16 Gene high mobility* group box 3 pseudogene 16*
HMGB3P17 Gene high mobility* group box 3 pseudogene 17*
HMGB3P10 Gene high mobility* group box 3 pseudogene 10*
HMGB3P11 Gene high mobility* group box 3 pseudogene 11*
HMGB3P12 Gene high mobility* group box 3 pseudogene 12*
HMGB3P13 Gene high mobility* group box 3 pseudogene 13*
HMGB3P18 Gene high mobility* group box 3 pseudogene 18*
HMGB3P19 Gene high mobility* group box 3 pseudogene 19*
HMGB3P29 Gene high mobility* group box 3 pseudogene 29*
HMGB3P28 Gene high mobility* group box 3 pseudogene 28*
HMGB3P21 Gene high mobility* group box 3 pseudogene 21*
HMGB3P23 Gene high mobility* group box 3 pseudogene 23*
HMGN2P4 Gene high mobility* group nucleosomal binding domain 2 pseudogene 4*
HMGN2P8 Gene high mobility* group nucleosomal binding domain 2 pseudogene 8*
TOX4P1 Gene TOX high mobility* group box family member 4 pseudogene 1*
limited mobility of proximal interphalangeal joint Gene Set From HPO Gene-Disease Associations genes associated with the limited mobility of proximal interphalangeal joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Limited Mobility Of Proximal Interphalangeal Joint Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Mobility Of Proximal Interphalangeal Joint in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
contracture of the proximal interphalangeal joint of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the contracture of the proximal interphalangeal joint of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Flexion Contracture Of Proximal Interphalangeal Joint Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Flexion Contracture Of Proximal Interphalangeal Joint in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
limited interphalangeal movement Gene Set From HPO Gene-Disease Associations genes associated with the limited interphalangeal movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Limited Interphalangeal Movement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Interphalangeal Movement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
diffuse scleroderma; limited scleroderma; scleroderma, diffuse; scleroderma, limited Gene Set From GAD Gene-Disease Associations genes associated with the disease diffuse scleroderma; limited scleroderma; scleroderma, diffuse; scleroderma, limited in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
limitation of joint mobility Gene Set From HPO Gene-Disease Associations genes associated with the limitation of joint mobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of hand joint mobility Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of hand joint mobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of joint mobility Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of joint mobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal joint mobility Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal joint mobility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
Limitation Of Joint Mobility Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limitation Of Joint Mobility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Hand Joint Mobility Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Hand Joint Mobility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
decreased joint mobility Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased joint mobility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal joint mobility Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal joint mobility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Joint mobility (Beighton score) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Joint mobility (Beighton score) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
interphalangeal joint contracture of finger Gene Set From HPO Gene-Disease Associations genes associated with the interphalangeal joint contracture of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
interphalangeal joint erosions Gene Set From HPO Gene-Disease Associations genes associated with the interphalangeal joint erosions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
contractures of the interphalangeal joint of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the contractures of the interphalangeal joint of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Interphalangeal Joint Contracture Of Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Interphalangeal Joint Contracture Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Interphalangeal Joint Erosions Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Interphalangeal Joint Erosions in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
swelling of proximal interphalangeal joints Gene Set From HPO Gene-Disease Associations genes associated with the swelling of proximal interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
enlarged proximal interphalangeal joints Gene Set From HPO Gene-Disease Associations genes associated with the enlarged proximal interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Enlarged Proximal Interphalangeal Joints Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Enlarged Proximal Interphalangeal Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Swelling Of Proximal Interphalangeal Joints Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Swelling Of Proximal Interphalangeal Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mobility Limitation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mobility Limitation from the curated CTD Gene-Disease Associations dataset.
periodontal attachment loss; periodontitis; tooth mobility Gene Set From GAD Gene-Disease Associations genes associated with the disease periodontal attachment loss; periodontitis; tooth mobility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dental occlusion, traumatic; periodontal attachment loss; periodontitis; tooth mobility Gene Set From GAD Gene-Disease Associations genes associated with the disease dental occlusion, traumatic; periodontal attachment loss; periodontitis; tooth mobility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mobility Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term mobility in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
decreased cervical spine mobility Gene Set From HPO Gene-Disease Associations genes associated with the decreased cervical spine mobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased finger mobility Gene Set From HPO Gene-Disease Associations genes associated with the decreased finger mobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limitation of knee mobility Gene Set From HPO Gene-Disease Associations genes associated with the limitation of knee mobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Tooth Mobility Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Tooth Mobility phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Mobility Limitation Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Mobility Limitation phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
High mobility group box domain Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the High mobility group box domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.
High mobility group, HMG-I/HMG-Y Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the High mobility group, HMG-I/HMG-Y protein domain from the InterPro Predicted Protein Domain Annotations dataset.
High mobility group nucleosome-binding domain-containing family Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the High mobility group nucleosome-binding domain-containing family protein domain from the InterPro Predicted Protein Domain Annotations dataset.
High mobility group box domain 5 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the High mobility group box domain 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
mobility Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term mobility in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
Mobility Limitation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mobility Limitation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Cervical Spine Mobility Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Cervical Spine Mobility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tumor Cell Mobility Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tumor Cell Mobility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limitation Of Knee Mobility Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limitation Of Knee Mobility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Finger Mobility Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Finger Mobility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
interphalangeal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term interphalangeal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
stiff interphalangeal joints Gene Set From HPO Gene-Disease Associations genes associated with the stiff interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent distal interphalangeal creases Gene Set From HPO Gene-Disease Associations genes associated with the absent distal interphalangeal creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypermobility of interphalangeal joints Gene Set From HPO Gene-Disease Associations genes associated with the hypermobility of interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
prominent interphalangeal joints Gene Set From HPO Gene-Disease Associations genes associated with the prominent interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
decreased movement range in interphalangeal joints Gene Set From HPO Gene-Disease Associations genes associated with the decreased movement range in interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
soft tissue swelling of interphalangeal joints Gene Set From HPO Gene-Disease Associations genes associated with the soft tissue swelling of interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
single interphalangeal crease of fifth finger Gene Set From HPO Gene-Disease Associations genes associated with the single interphalangeal crease of fifth finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypermobility of distal interphalangeal joints Gene Set From HPO Gene-Disease Associations genes associated with the hypermobility of distal interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
enlarged interphalangeal joints Gene Set From HPO Gene-Disease Associations genes associated with the enlarged interphalangeal joints phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent fourth finger distal interphalangeal crease Gene Set From HPO Gene-Disease Associations genes associated with the absent fourth finger distal interphalangeal crease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Interphalangeal Osteoarthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Interphalangeal Osteoarthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Absent Fourth Finger Distal Interphalangeal Crease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Absent Fourth Finger Distal Interphalangeal Crease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Stiff Interphalangeal Joints Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Stiff Interphalangeal Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prominent Interphalangeal Joints Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Prominent Interphalangeal Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Enlarged Interphalangeal Joints Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Enlarged Interphalangeal Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hypermobility Of Distal Interphalangeal Joints Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypermobility Of Distal Interphalangeal Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Soft Tissue Swelling Of Interphalangeal Joints Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Soft Tissue Swelling Of Interphalangeal Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Decreased Movement Range In Interphalangeal Joints Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Decreased Movement Range In Interphalangeal Joints in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absent Distal Interphalangeal Creases Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Distal Interphalangeal Creases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Single Interphalangeal Crease Of Fifth Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Single Interphalangeal Crease Of Fifth Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
limited scleroderma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease limited scleroderma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
scleroderma, diffuse; scleroderma, limited Gene Set From GAD Gene-Disease Associations genes associated with the disease scleroderma, diffuse; scleroderma, limited in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial male-limited precocious puberty. Gene Set From GAD Gene-Disease Associations genes associated with the disease familial male-limited precocious puberty. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
lung diseases, interstitial; scleroderma, diffuse; scleroderma, limited Gene Set From GAD Gene-Disease Associations genes associated with the disease lung diseases, interstitial; scleroderma, diffuse; scleroderma, limited in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
scleroderma, diffuse; scleroderma, limited; scleroderma, systemic Gene Set From GAD Gene-Disease Associations genes associated with the disease scleroderma, diffuse; scleroderma, limited; scleroderma, systemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
limited Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term limited in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
limited wrist movement Gene Set From HPO Gene-Disease Associations genes associated with the limited wrist movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limited elbow flexion/extension Gene Set From HPO Gene-Disease Associations genes associated with the limited elbow flexion/extension phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limited shoulder movement Gene Set From HPO Gene-Disease Associations genes associated with the limited shoulder movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limited neck range of motion Gene Set From HPO Gene-Disease Associations genes associated with the limited neck range of motion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limited elbow movement Gene Set From HPO Gene-Disease Associations genes associated with the limited elbow movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limited knee flexion Gene Set From HPO Gene-Disease Associations genes associated with the limited knee flexion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limited hip movement Gene Set From HPO Gene-Disease Associations genes associated with the limited hip movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limited neck flexion Gene Set From HPO Gene-Disease Associations genes associated with the limited neck flexion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limited pronation/supination of forearm Gene Set From HPO Gene-Disease Associations genes associated with the limited pronation/supination of forearm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limited elbow flexion Gene Set From HPO Gene-Disease Associations genes associated with the limited elbow flexion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limited knee flexion/extension Gene Set From HPO Gene-Disease Associations genes associated with the limited knee flexion/extension phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limited hip extension Gene Set From HPO Gene-Disease Associations genes associated with the limited hip extension phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
sex-limited autosomal dominant Gene Set From HPO Gene-Disease Associations genes associated with the sex-limited autosomal dominant phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limited knee extension Gene Set From HPO Gene-Disease Associations genes associated with the limited knee extension phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limited elbow extension Gene Set From HPO Gene-Disease Associations genes associated with the limited elbow extension phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limited extraocular movements Gene Set From HPO Gene-Disease Associations genes associated with the limited extraocular movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limited wrist extension Gene Set From HPO Gene-Disease Associations genes associated with the limited wrist extension phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Scleroderma, Limited Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Scleroderma, Limited phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Small Cell Lung Cancer Limited Stage Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Small Cell Lung Cancer Limited Stage in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dentinogenesis Imperfecta Limited To Primary Teeth Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dentinogenesis Imperfecta Limited To Primary Teeth in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Leydig Cell Adenoma, Somatic, With Male-Limited Precocious Puberty Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Leydig Cell Adenoma, Somatic, With Male-Limited Precocious Puberty in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Limited Knee Extension Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Knee Extension in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Neck Range Of Motion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Neck Range Of Motion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Elbow Extension Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Elbow Extension in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Elbow Movement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Elbow Movement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Extraocular Movements Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Extraocular Movements in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Hip Extension Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Hip Extension in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Hip Movement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Hip Movement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Pronation/Supination Of Forearm Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Pronation/Supination Of Forearm in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Wrist Extension Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Wrist Extension in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Knee Flexion/Extension Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Knee Flexion/Extension in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Knee Flexion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Knee Flexion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Elbow Flexion/Extension Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Elbow Flexion/Extension in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Shoulder Movement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Shoulder Movement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Elbow Extension And Supination Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Elbow Extension And Supination in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Neck Flexion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Neck Flexion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Elbow Flexion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Elbow Flexion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limited Wrist Movement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limited Wrist Movement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Familial male-limited precocious puberty Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Familial male-limited precocious puberty from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Limited scleroderma Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Limited scleroderma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Limited scleroderma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Limited scleroderma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Familial male-limited precocious puberty Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial male-limited precocious puberty in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Self-limited epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Self-limited epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Self-limited familial infantile epilepsy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Self-limited familial infantile epilepsy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Limited cutaneous systemic scleroderma Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Limited cutaneous systemic scleroderma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Chondrodysplasia with joint dislocations, GPAPP type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Chondrodysplasia with joint dislocations, GPAPP type 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.
Corneal fragility keratoglobus, blue sclerae AND joint hypermobility Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Corneal fragility keratoglobus, blue sclerae AND joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Temporomandibular Joint Dysfunction Syndrome Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Temporomandibular Joint Dysfunction Syndrome from the curated CTD Gene-Disease Associations dataset.
Temporomandibular Joint Disorders Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Temporomandibular Joint Disorders from the curated CTD Gene-Disease Associations dataset.
Joint Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Joint Diseases from the curated CTD Gene-Disease Associations dataset.
Joint Instability Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Joint Instability 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.
Histiocytosis with joint contractures and sensorineural deafness Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Histiocytosis with joint contractures and sensorineural deafness from the curated CTD Gene-Disease Associations dataset.
gastrointestinal diseases; henoch-schoenlein purpura; joint diseases; kidney diseases; proteinuria; purpura, schoenlein-henoch Gene Set From GAD Gene-Disease Associations genes associated with the disease gastrointestinal diseases; henoch-schoenlein purpura; joint diseases; kidney diseases; proteinuria; purpura, schoenlein-henoch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
degenerative arthropathy ; facial pain; osteoarthritis; temporomandibular joint disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease degenerative arthropathy ; facial pain; osteoarthritis; temporomandibular joint disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemochromatosis; iron overload; joint diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease hemochromatosis; iron overload; joint diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis Gene Set From GAD Gene-Disease Associations genes associated with the disease colitis, ulcerative; crohn disease; eye diseases; inflammatory bowel diseases; joint diseases; liver diseases; skin diseases; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hip dislocation, congenital; joint instability Gene Set From GAD Gene-Disease Associations genes associated with the disease hip dislocation, congenital; joint instability in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemochromatosis; joint diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease hemochromatosis; joint diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
temporomandibular joint disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease temporomandibular joint disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
pain; temporomandibular joint disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease pain; temporomandibular joint disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hemochromatosis; joint diseases; rheumatic diseases; rheumatism Gene Set From GAD Gene-Disease Associations genes associated with the disease hemochromatosis; joint diseases; rheumatic diseases; rheumatism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
temporomandibular joint pain Gene Set From GAD Gene-Disease Associations genes associated with the disease temporomandibular joint pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fatigue; hemochromatosis; joint diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease fatigue; hemochromatosis; joint diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
degenerative arthropathy ; osteoarthritis; temporomandibular joint disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease degenerative arthropathy ; osteoarthritis; temporomandibular joint disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
joint Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term joint in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
limb joint morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the limb joint morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
embryonic skeletal joint morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the embryonic skeletal joint morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
embryonic skeletal limb joint morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the embryonic skeletal limb joint morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
embryonic skeletal joint development Gene Set From GO Biological Process Annotations 2015 genes participating in the embryonic skeletal joint development biological process from the curated GO Biological Process Annotations 2015 dataset.
Temporomandibular joint disorders Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Temporomandibular joint disorders phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
abnormal joint morphology Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormal joint morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of lower limb joint Gene Set From GWASdb SNP-Phenotype Associations genes associated with the abnormality of lower limb joint phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
costochondral joint sclerosis Gene Set From GWASdb SNP-Phenotype Associations genes associated with the costochondral joint sclerosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
abnormality of metacarpophalangeal joint Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of metacarpophalangeal joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
lower extremity joint dislocation Gene Set From HPO Gene-Disease Associations genes associated with the lower extremity joint dislocation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the hip joint Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the hip joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the sacroiliac joint Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the sacroiliac joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
joint hyperflexibility Gene Set From HPO Gene-Disease Associations genes associated with the joint hyperflexibility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
joint hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the joint hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of upper limb joint Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of upper limb joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
joint contracture of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the joint contracture of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multiple joint contractures Gene Set From HPO Gene-Disease Associations genes associated with the multiple joint contractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
joint contractures involving the joints of the feet Gene Set From HPO Gene-Disease Associations genes associated with the joint contractures involving the joints of the feet phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
joint dislocation Gene Set From HPO Gene-Disease Associations genes associated with the joint dislocation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
large joint dislocations Gene Set From HPO Gene-Disease Associations genes associated with the large joint dislocations phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
joint swelling Gene Set From HPO Gene-Disease Associations genes associated with the joint swelling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormal joint morphology Gene Set From HPO Gene-Disease Associations genes associated with the abnormal joint morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
joint swelling onset late infancy Gene Set From HPO Gene-Disease Associations genes associated with the joint swelling onset late infancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
joint contracture of the hand Gene Set From HPO Gene-Disease Associations genes associated with the joint contracture of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
degenerative joint disease Gene Set From HPO Gene-Disease Associations genes associated with the degenerative joint disease phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
joint laxity Gene Set From HPO Gene-Disease Associations genes associated with the joint laxity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
limb joint contracture Gene Set From HPO Gene-Disease Associations genes associated with the limb joint contracture phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
joint stiffness Gene Set From HPO Gene-Disease Associations genes associated with the joint stiffness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
joint hypermobility Gene Set From HPO Gene-Disease Associations genes associated with the joint hypermobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
finger joint hypermobility Gene Set From HPO Gene-Disease Associations genes associated with the finger joint hypermobility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of lower limb joint Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of lower limb joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the humeroradial joint Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the humeroradial joint phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
finger joint hyperextensibility Gene Set From HPO Gene-Disease Associations genes associated with the finger joint hyperextensibility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
generalized joint laxity Gene Set From HPO Gene-Disease Associations genes associated with the generalized joint laxity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
metacarpophalangeal joint hyperextensibility Gene Set From HPO Gene-Disease Associations genes associated with the metacarpophalangeal joint hyperextensibility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
upper extremity joint dislocation Gene Set From HPO Gene-Disease Associations genes associated with the upper extremity joint dislocation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Joint Instability Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Joint Instability phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Temporomandibular Joint Disorders Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Temporomandibular Joint Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Joint Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Joint Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
decreased susceptibility to induced joint inflammation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased susceptibility to induced joint inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal temporomandibular joint morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal temporomandibular joint morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
chronic joint inflammation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the chronic joint inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal joint morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal joint morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
joint swelling Gene Set From MPO Gene-Phenotype Associations gene mutations causing the joint swelling phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
calcified joint Gene Set From MPO Gene-Phenotype Associations gene mutations causing the calcified joint phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
joint inflammation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the joint inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal joint capsule morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal joint capsule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures Gene Set From OMIM Gene-Disease Associations genes associated with the spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures phenotype from the curated OMIM Gene-Disease Associations dataset.
chondrodysplasia with joint dislocations, grapp type Gene Set From OMIM Gene-Disease Associations genes associated with the chondrodysplasia with joint dislocations, grapp type 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.
multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set From OMIM Gene-Disease Associations genes associated with the multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.
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.
joint Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue joint from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
temporomandibular joint Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue temporomandibular joint in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
hinge joint Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hinge joint in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
femorotibial joint Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue femorotibial joint in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
joint Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue joint in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
hip joint Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hip joint in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
ankle joint Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue ankle joint in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Knee Joint Valgus Deformity Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Knee Joint Valgus Deformity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Prosthetic Joint Infection Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Prosthetic Joint Infection in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Inflammatory Joint Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Inflammatory Joint Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Joint Contracture Of The 5Th Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Joint Contracture Of The 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Instability Of Atlantooccipital Joint Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Instability Of Atlantooccipital Joint in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple Joint Dislocations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple Joint Dislocations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Temporomandibular Joint Dysfunction Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Temporomandibular Joint Dysfunction Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Temporomandibular Joint Osteoarthritis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Temporomandibular Joint Osteoarthritis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Facet Joint Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facet Joint Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Histiocytosis With Joint Contractures And Sensorineural Deafness Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Histiocytosis With Joint Contractures And Sensorineural Deafness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Hip Joint Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Hip Joint in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autoimmune Interstitial Lung, Joint, And Kidney Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autoimmune Interstitial Lung, Joint, And Kidney Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Focal Palmoplantar Keratoderma With Joint Keratoses Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Focal Palmoplantar Keratoderma With Joint Keratoses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Facet Joint Arthrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facet Joint Arthrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Ankylosis Of The Elbow Joint Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Ankylosis Of The Elbow Joint in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of Lower Limb Joint Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Lower Limb Joint in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Joint Laxity, Short Stature, And Myopia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Joint Laxity, Short Stature, And Myopia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Joint Tuberculosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Joint Tuberculosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Joint Swelling Inflammatory Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Joint Swelling Inflammatory in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intermittent Joint Effusion Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intermittent Joint Effusion in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Joint Function Disorder Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Joint Function Disorder in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Derangement Of Temporomandibular Joint Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Derangement Of Temporomandibular Joint in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rheumatic Joint Disease Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rheumatic Joint Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Joint Spaces Of The Elbow Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Joint Spaces Of The Elbow in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Joint Hyperflexibility Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Joint Hyperflexibility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limb Joint Contracture Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limb Joint Contracture in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Joint Laxity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Joint Laxity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Knee Joint Laxity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Knee Joint Laxity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hip Joint Pain Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hip Joint Pain in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Joint Stiffness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Joint Stiffness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Hip Joint Varus Deformity - Observation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hip Joint Varus Deformity - Observation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Range Of Joint Movement Increased Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Range Of Joint Movement Increased in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Joint Swelling Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Joint Swelling in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Generalized Joint Laxity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Generalized Joint Laxity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Joint Tenderness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Joint Tenderness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multiple Joint Dislocations Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multiple Joint Dislocations in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Finger Joint Hypermobility Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Finger Joint Hypermobility in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Joint Instability Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Joint Instability in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Distal Joint Laxity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Distal Joint Laxity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Sacroiliac Joint Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Sacroiliac Joint in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Temporomandibular Joint Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Temporomandibular Joint in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Joint Morphology Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Joint Morphology in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Temporomandibular Joint Internal Derangement Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Temporomandibular Joint Internal Derangement in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Lower Extremity Joint Dislocation Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lower Extremity Joint Dislocation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of Upper Limb Joint Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Upper Limb Joint in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
embryonic skeletal joint development Gene Set From GO Biological Process Annotations 2023 genes participating in the embryonic skeletal joint development biological process from the curated GO Biological Process Annotations 2023 dataset.
embryonic skeletal joint morphogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the embryonic skeletal joint morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
embryonic skeletal limb joint morphogenesis Gene Set From GO Biological Process Annotations 2023 genes participating in the embryonic skeletal limb joint morphogenesis biological process from the curated GO Biological Process Annotations 2023 dataset.
abnormal sternocostal joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sternocostal joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal costovertebral joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal costovertebral joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
joint swelling Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the joint swelling phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
calcified joint Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the calcified joint phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal synovial joint cavity morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal synovial joint cavity morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent temporomandibular joint Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent temporomandibular joint phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal incudostapedial joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal incudostapedial joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal incudomalleolar joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal incudomalleolar joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal rib joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal rib joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal knee joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal knee joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal costochondral joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal costochondral joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
joint contracture Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the joint contracture phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
joint inflammation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the joint inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
chronic joint inflammation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the chronic joint inflammation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
accelerated temporomandibular joint osteoarthritis Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the accelerated temporomandibular joint osteoarthritis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal elbow joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal elbow joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal hip joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hip joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal synovial joint capsule morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal synovial joint capsule morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
joint dislocation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the joint dislocation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal shoulder joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal shoulder joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent temporomandibular joint disk Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent temporomandibular joint disk phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
joint laxity Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the joint laxity phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal temporomandibular joint disk morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal temporomandibular joint disk morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent costovertebral joint Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent costovertebral joint phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
atlanto-occipital joint dislocation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the atlanto-occipital joint dislocation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal temporomandibular joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal temporomandibular joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal hindlimb joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hindlimb joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal wrist joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal wrist joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal ankle joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ankle joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal forelimb joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal forelimb joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal hand joint morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hand joint morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal joint morphology Gene Set From IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal joint morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset.
embryonic skeletal joint development Gene Set From GO Biological Process Annotations 2025 genes participating in the embryonic skeletal joint development biological process from the curated GO Biological Process Annotations 2025 dataset.
embryonic skeletal joint morphogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the embryonic skeletal joint morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
embryonic skeletal limb joint morphogenesis Gene Set From GO Biological Process Annotations 2025 genes participating in the embryonic skeletal limb joint morphogenesis biological process from the curated GO Biological Process Annotations 2025 dataset.
Spondyloepiphyseal dysplasia with congenital joint dislocations Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Spondyloepiphyseal dysplasia with congenital joint dislocations from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Spondyloepimetaphyseal dysplasia with joint laxity type 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spondyloepimetaphyseal dysplasia with joint laxity type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spondyloepimetaphyseal dysplasia with joint laxity Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spondyloepimetaphyseal dysplasia with joint laxity in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autoimmune interstitial lung, joint, and kidney disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autoimmune interstitial lung, joint, and kidney disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spondyloepiphyseal dysplasia with congenital joint dislocations Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spondyloepiphyseal dysplasia with congenital joint dislocations in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spondyloepimetaphyseal dysplasia with joint laxity type 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spondyloepimetaphyseal dysplasia with joint laxity type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Chondrodysplasia with joint dislocations gPAPP type Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Chondrodysplasia with joint dislocations gPAPP type in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Spondyloepimetaphyseal dysplasia with joint laxity type 3 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Spondyloepimetaphyseal dysplasia with joint laxity type 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Joint Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Joint from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Joint Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Joint in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Hip joint Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hip joint in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Temporomandibular joint Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Temporomandibular joint in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Ankle joint Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Ankle joint in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Hinge joint Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hinge joint in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Femorotibial joint Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Femorotibial joint in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Joint hypermobility Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Joint hypermobility phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lower-limb joint contracture Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lower-limb joint contracture phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
MULTIPLE JOINT DISLOCATI Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the MULTIPLE JOINT DISLOCATI phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple joint dislocations Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple joint dislocations phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Joint laxity Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Joint laxity phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multiple joint contractures Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multiple joint contractures phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Joint dislocation Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Joint dislocation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Joint damage progression in ACPA-negative rheumatoid arthritis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Joint damage progression in ACPA-negative rheumatoid arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Spherical equivalent (joint analysis main effects and education interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Spherical equivalent (joint analysis main effects and education interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Aseptic loosening in total joint arthroplasty Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Aseptic loosening in total joint arthroplasty phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Temporomandibular joint disorder Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Temporomandibular joint disorder phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
joint destruction in rheumatoid arthritis (rapid vs slow) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the joint destruction in rheumatoid arthritis (rapid vs slow) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to TNF inhibitor in rheumatoid arthritis (change in swollen 28-joint count) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to TNF inhibitor in rheumatoid arthritis (change in swollen 28-joint count) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to TNF inhibitor in rheumatoid arthritis (change in tender 28-joint count) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to TNF inhibitor in rheumatoid arthritis (change in tender 28-joint count) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Hip minimal joint space width Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hip minimal joint space width phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Osteoarthritis of the hip or knee (with total joint replacement) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Osteoarthritis of the hip or knee (with total joint replacement) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Joint damage in rheumatoid arthritis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Joint damage in rheumatoid arthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist circumference adjusted for BMI (joint analysis main effects and smoking interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist circumference adjusted for BMI (joint analysis main effects and smoking interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI (joint analysis main effects and smoking interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI (joint analysis main effects and smoking interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist circumference adjusted for BMI (joint analysis main effects and physical activity interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist circumference adjusted for BMI (joint analysis main effects and physical activity interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body mass index (joint analysis main effects and physical activity interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (joint analysis main effects and physical activity interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Body mass index (joint analysis main effects and smoking interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Body mass index (joint analysis main effects and smoking interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Waist-to-hip ratio adjusted for BMI (joint analysis for main effect and physical activity interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Waist-to-hip ratio adjusted for BMI (joint analysis for main effect and physical activity interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Possible neuropathic pain in post total joint replacement surgery for osteoarthritis Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Possible neuropathic pain in post total joint replacement surgery for osteoarthritis phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Symphalangism, proximal, 1b Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Symphalangism, proximal, 1b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Spinal Muscular Atrophy, Proximal, Adult, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation from the curated CTD Gene-Disease Associations dataset.
vulvar proximal-type epithelioid sarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease vulvar proximal-type epithelioid sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
H3K4me3_epithelial cell of proximal tubule_hg19_2 Gene Set From ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_epithelial cell of proximal tubule_hg19_2 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.
H3K4me3_epithelial cell of proximal tubule_hg19_1 Gene Set From ENCODE Histone Modification Site Profiles genes with high histone modification abundance in the H3K4me3_epithelial cell of proximal tubule_hg19_1 histone modification site profile from the ENCODE Histone Modification Site Profiles dataset.
CTCF_epithelial cell of proximal tubule_hg19_1 Gene Set From ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_epithelial cell of proximal tubule_hg19_1 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.
CTCF_epithelial cell of proximal tubule_hg19_2 Gene Set From ENCODE Transcription Factor Binding Site Profiles genes with transcription factor binding evidence in the CTCF_epithelial cell of proximal tubule_hg19_2 transcription factor binding site profile from the ENCODE Transcription Factor Binding Site Profiles dataset.
proximal chromosome 9p to q and distal chromosome 9q Gene Set From GAD Gene-Disease Associations genes associated with the disease proximal chromosome 9p to q and distal chromosome 9q in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
fractures, bone; hip fractures; proximal humeral fractures; shoulder fractures; wrist injuries Gene Set From GAD Gene-Disease Associations genes associated with the disease fractures, bone; hip fractures; proximal humeral fractures; shoulder fractures; wrist injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
proximal Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term proximal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
LMX1B_KO_GDS3320_57_mouse_embryonic (e11.5) proximal hindlimb bud tissues Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the LMX1B_KO_GDS3320_57_mouse_embryonic (e11.5) proximal hindlimb bud tissues gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
proximal/distal pattern formation involved in nephron development Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation involved in nephron development biological process from the curated GO Biological Process Annotations 2015 dataset.
proximal convoluted tubule segment 2 development Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal convoluted tubule segment 2 development biological process from the curated GO Biological Process Annotations 2015 dataset.
proximal/distal pattern formation involved in metanephric nephron development Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation involved in metanephric nephron development biological process from the curated GO Biological Process Annotations 2015 dataset.
proximal tubule development Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal tubule development biological process from the curated GO Biological Process Annotations 2015 dataset.
metanephric proximal convoluted tubule segment 2 development Gene Set From GO Biological Process Annotations 2015 genes participating in the metanephric proximal convoluted tubule segment 2 development biological process from the curated GO Biological Process Annotations 2015 dataset.
lung proximal/distal axis specification Gene Set From GO Biological Process Annotations 2015 genes participating in the lung proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2015 dataset.
polarity specification of proximal/distal axis Gene Set From GO Biological Process Annotations 2015 genes participating in the polarity specification of proximal/distal axis biological process from the curated GO Biological Process Annotations 2015 dataset.
proximal/distal axis specification Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2015 dataset.
proximal straight tubule development Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal straight tubule development biological process from the curated GO Biological Process Annotations 2015 dataset.
metanephric proximal tubule development Gene Set From GO Biological Process Annotations 2015 genes participating in the metanephric proximal tubule development biological process from the curated GO Biological Process Annotations 2015 dataset.
metanephric proximal convoluted tubule development Gene Set From GO Biological Process Annotations 2015 genes participating in the metanephric proximal convoluted tubule development biological process from the curated GO Biological Process Annotations 2015 dataset.
proximal/distal pattern formation Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2015 dataset.
proximal convoluted tubule development Gene Set From GO Biological Process Annotations 2015 genes participating in the proximal convoluted tubule development biological process from the curated GO Biological Process Annotations 2015 dataset.
metanephric proximal straight tubule development Gene Set From GO Biological Process Annotations 2015 genes participating in the metanephric proximal straight tubule development biological process from the curated GO Biological Process Annotations 2015 dataset.
core promoter proximal region dna binding Gene Set From GO Molecular Function Annotations 2015 genes performing the core promoter proximal region dna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
rna polymerase ii core promoter proximal region sequence-specific dna binding transcription factor activity Gene Set From GO Molecular Function Annotations 2015 genes performing the rna polymerase ii core promoter proximal region sequence-specific dna binding transcription factor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset.
rna polymerase ii core promoter proximal region sequence-specific dna binding transcription factor activity involved in positive regulation of transcription Gene Set From GO Molecular Function Annotations 2015 genes performing the rna polymerase ii core promoter proximal region sequence-specific dna binding transcription factor activity involved in positive regulation of transcription molecular function from the curated GO Molecular Function Annotations 2015 dataset.
rna polymerase ii core promoter proximal region sequence-specific dna binding Gene Set From GO Molecular Function Annotations 2015 genes performing the rna polymerase ii core promoter proximal region sequence-specific dna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
rna polymerase ii core promoter proximal region sequence-specific dna binding transcription factor activity involved in negative regulation of transcription Gene Set From GO Molecular Function Annotations 2015 genes performing the rna polymerase ii core promoter proximal region sequence-specific dna binding transcription factor activity involved in negative regulation of transcription molecular function from the curated GO Molecular Function Annotations 2015 dataset.
core promoter proximal region sequence-specific dna binding Gene Set From GO Molecular Function Annotations 2015 genes performing the core promoter proximal region sequence-specific dna binding molecular function from the curated GO Molecular Function Annotations 2015 dataset.
proximal tapering of metacarpals Gene Set From HPO Gene-Disease Associations genes associated with the proximal tapering of metacarpals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
small proximal tibial epiphyses Gene Set From HPO Gene-Disease Associations genes associated with the small proximal tibial epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal amyotrophy Gene Set From HPO Gene-Disease Associations genes associated with the proximal amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
enlarged epiphysis of the proximal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
enlarged epiphyses of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the enlarged epiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short metacarpals with rounded proximal ends Gene Set From HPO Gene-Disease Associations genes associated with the short metacarpals with rounded proximal ends phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
club-shaped proximal femur Gene Set From HPO Gene-Disease Associations genes associated with the club-shaped proximal femur phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
slender proximal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the slender proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the proximal tibial epiphysis Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the proximal tibial epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular shaped proximal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the triangular shaped proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the proximal phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
late-onset proximal muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the late-onset proximal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal fibular overgrowth Gene Set From HPO Gene-Disease Associations genes associated with the proximal fibular overgrowth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multicentric ossification of proximal femoral epiphyses Gene Set From HPO Gene-Disease Associations genes associated with the multicentric ossification of proximal femoral epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
multicentric ossification of proximal humeral epiphyses Gene Set From HPO Gene-Disease Associations genes associated with the multicentric ossification of proximal humeral epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal renal tubular acidosis Gene Set From HPO Gene-Disease Associations genes associated with the proximal renal tubular acidosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
long proximal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the long proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal placement of thumb Gene Set From HPO Gene-Disease Associations genes associated with the proximal placement of thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
widened proximal tibial metaphyses Gene Set From HPO Gene-Disease Associations genes associated with the widened proximal tibial metaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular shaped proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the triangular shaped proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypersegmentation of proximal phalanx of second finger Gene Set From HPO Gene-Disease Associations genes associated with the hypersegmentation of proximal phalanx of second finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
shortening of all proximal phalanges of the fingers Gene Set From HPO Gene-Disease Associations genes associated with the shortening of all proximal phalanges of the fingers phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
complete duplication of proximal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the complete duplication of proximal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular epiphyses of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the triangular epiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal tibial hypopolasia Gene Set From HPO Gene-Disease Associations genes associated with the proximal tibial hypopolasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of proximal fibula Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of proximal fibula phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pointed proximal second through fifth metacarpals Gene Set From HPO Gene-Disease Associations genes associated with the pointed proximal second through fifth metacarpals phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the proximal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the proximal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent proximal phalanx of thumb Gene Set From HPO Gene-Disease Associations genes associated with the absent proximal phalanx of thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short proximal phalanx of finger Gene Set From HPO Gene-Disease Associations genes associated with the short proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
absent proximal finger flexion creases Gene Set From HPO Gene-Disease Associations genes associated with the absent proximal finger flexion creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal femoral epiphysiolysis Gene Set From HPO Gene-Disease Associations genes associated with the proximal femoral epiphysiolysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the proximal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the proximal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the proximal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the proximal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
non-acidotic proximal tubulopathy Gene Set From HPO Gene-Disease Associations genes associated with the non-acidotic proximal tubulopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal/middle symphalangism of 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the proximal/middle symphalangism of 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
stippled calcification proximal humeral epiphyses Gene Set From HPO Gene-Disease Associations genes associated with the stippled calcification proximal humeral epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal femoral metaphyseal abnormality Gene Set From HPO Gene-Disease Associations genes associated with the proximal femoral metaphyseal abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tombstone-shaped proximal phalanges Gene Set From HPO Gene-Disease Associations genes associated with the tombstone-shaped proximal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal symphalangism Gene Set From HPO Gene-Disease Associations genes associated with the proximal symphalangism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal upper limb amyotrophy Gene Set From HPO Gene-Disease Associations genes associated with the proximal upper limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the epiphyses of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the epiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular epiphysis of the proximal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the triangular epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
symphalangism affecting the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the symphalangism affecting the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
mottled pigmentation of the trunk and proximal extremities Gene Set From HPO Gene-Disease Associations genes associated with the mottled pigmentation of the trunk and proximal extremities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular epiphysis of the proximal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the triangular epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the epiphysis of the proximal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the proximal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal muscle weakness in lower limbs Gene Set From HPO Gene-Disease Associations genes associated with the proximal muscle weakness in lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal radio-ulnar synostosis Gene Set From HPO Gene-Disease Associations genes associated with the proximal radio-ulnar synostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short proximal phalanx of thumb Gene Set From HPO Gene-Disease Associations genes associated with the short proximal phalanx of thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
metaphyseal cupping of proximal phalanges Gene Set From HPO Gene-Disease Associations genes associated with the metaphyseal cupping of proximal phalanges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive proximal muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the progressive proximal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
irregular proximal tibial epiphyses Gene Set From HPO Gene-Disease Associations genes associated with the irregular proximal tibial epiphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the proximal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal muscle weakness Gene Set From HPO Gene-Disease Associations genes associated with the proximal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal femoral metaphyseal irregularity Gene Set From HPO Gene-Disease Associations genes associated with the proximal femoral metaphyseal irregularity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
duplication of the proximal phalanx of the hallux Gene Set From HPO Gene-Disease Associations genes associated with the duplication of the proximal phalanx of the hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal tubulopathy Gene Set From HPO Gene-Disease Associations genes associated with the proximal tubulopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
short proximal phalanx of hallux Gene Set From HPO Gene-Disease Associations genes associated with the short proximal phalanx of hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cone-shaped epiphyses of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the cone-shaped epiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thin proximal phalanges with broad epiphyses of the hand Gene Set From HPO Gene-Disease Associations genes associated with the thin proximal phalanges with broad epiphyses of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypoplasia of proximal radius Gene Set From HPO Gene-Disease Associations genes associated with the hypoplasia of proximal radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
symphalangism affecting the proximal phalanx of the 5th finger Gene Set From HPO Gene-Disease Associations genes associated with the symphalangism affecting the proximal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal muscle weakness in upper limbs Gene Set From HPO Gene-Disease Associations genes associated with the proximal muscle weakness in upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
enlargement of the proximal femoral epiphysis Gene Set From HPO Gene-Disease Associations genes associated with the enlargement of the proximal femoral epiphysis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
triangular shaped proximal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the triangular shaped proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
hypersegmentation of proximal phalanx of third finger Gene Set From HPO Gene-Disease Associations genes associated with the hypersegmentation of proximal phalanx of third finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
enlarged epiphysis of the proximal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the enlarged epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the proximal phalanx of the thumb Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal lower limb amyotrophy Gene Set From HPO Gene-Disease Associations genes associated with the proximal lower limb amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the epiphysis of the proximal phalanx of the 2nd finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the epiphysis of the proximal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the proximal phalanx of the 3rd finger Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the proximal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pseudoepiphyses of the proximal phalanges of the hand Gene Set From HPO Gene-Disease Associations genes associated with the pseudoepiphyses of the proximal phalanges of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
proximal symphalangism (hands) Gene Set From HPO Gene-Disease Associations genes associated with the proximal symphalangism (hands) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dilated proximal convoluted tubules Gene Set From MPO Gene-Phenotype Associations gene mutations causing the dilated proximal convoluted tubules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent proximal rib Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent proximal rib phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
proximal convoluted tubule brush border loss Gene Set From MPO Gene-Phenotype Associations gene mutations causing the proximal convoluted tubule brush border loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal proximal convoluted tubule brush border morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal proximal convoluted tubule brush border morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal proximal-distal axis patterning Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal proximal-distal axis patterning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal proximal convoluted tubule morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal proximal convoluted tubule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent proximal convoluted tubule brush border Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent proximal convoluted tubule brush border phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
symphalangism, proximal, 1b Gene Set From OMIM Gene-Disease Associations genes associated with the symphalangism, proximal, 1b phenotype from the curated OMIM Gene-Disease Associations dataset.
symphalangism, proximal Gene Set From OMIM Gene-Disease Associations genes associated with the symphalangism, proximal phenotype from the curated OMIM Gene-Disease Associations dataset.
myopathy, proximal, with early respiratory muscle involvement Gene Set From OMIM Gene-Disease Associations genes associated with the myopathy, proximal, with early respiratory muscle involvement phenotype from the curated OMIM Gene-Disease Associations dataset.
hereditary motor and sensory neuropathy, proximal type Gene Set From OMIM Gene-Disease Associations genes associated with the hereditary motor and sensory neuropathy, proximal type phenotype from the curated OMIM Gene-Disease Associations dataset.
renal tubular acidosis, proximal, with ocular abnormalities Gene Set From OMIM Gene-Disease Associations genes associated with the renal tubular acidosis, proximal, with ocular abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.
renal proximal tubule Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue renal proximal tubule from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.
renal proximal tubule Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue renal proximal tubule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
proximal deep inguinal lymph node Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue proximal deep inguinal lymph node in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Dissection Of Proximal Aorta Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dissection Of Proximal Aorta in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hmn (Hereditary Motor Neuropathy) Proximal Type I Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hmn (Hereditary Motor Neuropathy) Proximal Type I in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proximal Spinal Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proximal Spinal Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proximal Amyotrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proximal Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Asymmetric Diabetic Proximal Motor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Asymmetric Diabetic Proximal Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Symmetric Diabetic Proximal Motor Neuropathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Symmetric Diabetic Proximal Motor Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proximal Myopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proximal Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proximal-Type Epithelioid Sarcoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proximal-Type Epithelioid Sarcoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proximal Myopathy With Focal Depletion Of Mitochondria Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proximal Myopathy With Focal Depletion Of Mitochondria in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Complete Duplication Of Proximal Phalanx Of The Thumb Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Complete Duplication Of Proximal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proximal Symphalangism Of Hands Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proximal Symphalangism Of Hands in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Proximal Femoral Metaphyseal Abnormality Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Proximal Femoral Metaphyseal Abnormality in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Irregular Proximal Tibial Epiphyses Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Irregular Proximal Tibial Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Small Proximal Tibial Epiphyses Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Small Proximal Tibial Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Shortening Of All Proximal Phalanges Of The Fingers Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Shortening Of All Proximal Phalanges Of The Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypersegmentation Of Proximal Phalanx Of Second Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypersegmentation Of Proximal Phalanx Of Second Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypersegmentation Of Proximal Phalanx Of Third Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypersegmentation Of Proximal Phalanx Of Third Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Triangular Epiphysis Of The Proximal Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Triangular Epiphysis Of The Proximal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Triangular Shaped Proximal Phalanx Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Triangular Shaped Proximal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thin Proximal Phalanges With Broad Epiphyses Of The Hand Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thin Proximal Phalanges With Broad Epiphyses Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Long Proximal Phalanx Of Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Long Proximal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Slender Proximal Phalanx Of Finger Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Slender Proximal Phalanx Of Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Non-Acidotic Proximal Tubulopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Non-Acidotic Proximal Tubulopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Duplication Of The Proximal Phalanx Of The Hallux Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Duplication Of The Proximal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Proximal Myelopathic Muscular Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Proximal Myelopathic Muscular Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Proximal Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Progressive Proximal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fatiguable Weakness Of Proximal Limb Muscles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fatiguable Weakness Of Proximal Limb Muscles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Metacarpals With Rounded Proximal Ends Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Metacarpals With Rounded Proximal Ends in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Tubulopathy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Tubulopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Placement Of Thumb Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Placement Of Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Muscle Weakness In Lower Limbs Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Muscle Weakness In Lower Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Muscle Weakness In Upper Limbs Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Muscle Weakness In Upper Limbs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Delayed Proximal Femoral Epiphyseal Ossification Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Delayed Proximal Femoral Epiphyseal Ossification in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal/Middle Symphalangism Of 5Th Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal/Middle Symphalangism Of 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of The Proximal Phalanges Of The Hand Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Proximal Phalanges Of The Hand in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Short Proximal Phalanx Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Short Proximal Phalanx in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Widened Proximal Tibial Metaphyses Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Widened Proximal Tibial Metaphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Late-Onset Proximal Muscle Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Late-Onset Proximal Muscle Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Fibular Overgrowth Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Fibular Overgrowth in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Lower Limb Amyotrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Lower Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Enlargement Of The Proximal Femoral Epiphysis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Enlargement Of The Proximal Femoral Epiphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absent Proximal Finger Flexion Creases Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Proximal Finger Flexion Creases in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Femoral Metaphyseal Irregularity Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Femoral Metaphyseal Irregularity in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Weakness Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Weakness in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Partial Duplication Of The Proximal Phalanx Of The 3Rd Finger Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Partial Duplication Of The Proximal Phalanx Of The 3Rd Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Radio-Ulnar Synostosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Radio-Ulnar Synostosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Metaphyseal Cupping Of Proximal Phalanges Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Metaphyseal Cupping Of Proximal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Club-Shaped Proximal Femur Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Club-Shaped Proximal Femur in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multicentric Ossification Of Proximal Femoral Epiphyses Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multicentric Ossification Of Proximal Femoral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Multicentric Ossification Of Proximal Humeral Epiphyses Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Multicentric Ossification Of Proximal Humeral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Upper Limb Amyotrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Upper Limb Amyotrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Absent Proximal Phalanx Of Thumb Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Proximal Phalanx Of Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Tombstone-Shaped Proximal Phalanges Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Tombstone-Shaped Proximal Phalanges in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Pointed Proximal Second Through Fifth Metacarpals Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pointed Proximal Second Through Fifth Metacarpals in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Tibial And Fibular Fusion Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Tibial And Fibular Fusion in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Stippled Calcification Proximal Humeral Epiphyses Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Stippled Calcification Proximal Humeral Epiphyses in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Tapering Of Metacarpals Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Tapering Of Metacarpals in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Tibial Hypoplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Tibial Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Mottled Pigmentation Of The Trunk And Proximal Extremities Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Mottled Pigmentation Of The Trunk And Proximal Extremities in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Proximal Upper Limb Muscle Hypertrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Proximal Upper Limb Muscle Hypertrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Proximal Phalanx Of The Thumb Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Proximal Phalanx Of The Thumb in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Broad Proximal Phalanx Of The Hallux Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Broad Proximal Phalanx Of The Hallux in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Wide Proximal Femoral Metaphysis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wide Proximal Femoral Metaphysis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
proximal/distal pattern formation Gene Set From GO Biological Process Annotations 2023 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2023 dataset.
proximal/distal axis specification Gene Set From GO Biological Process Annotations 2023 genes participating in the proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2023 dataset.
metanephric proximal tubule development Gene Set From GO Biological Process Annotations 2023 genes participating in the metanephric proximal tubule development biological process from the curated GO Biological Process Annotations 2023 dataset.
proximal tubule development Gene Set From GO Biological Process Annotations 2023 genes participating in the proximal tubule development biological process from the curated GO Biological Process Annotations 2023 dataset.
proximal dendrite Gene Set From GO Cellular Component Annotations 2023 proteins localized to the proximal dendrite cellular component from the curated GO Cellular Component Annotations 2023 dataset.
proximal neuron projection Gene Set From GO Cellular Component Annotations 2023 proteins localized to the proximal neuron projection cellular component from the curated GO Cellular Component Annotations 2023 dataset.
abnormal proximal convoluted tubule morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal proximal convoluted tubule morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent proximal convoluted tubule brush border Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent proximal convoluted tubule brush border phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent proximal rib Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent proximal rib phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
dilated proximal convoluted tubule Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated proximal convoluted tubule phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal proximal-distal axis patterning Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal proximal-distal axis patterning phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
proximal convoluted tubule brush border loss Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the proximal convoluted tubule brush border loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal proximal convoluted tubule brush border morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal proximal convoluted tubule brush border morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Human - Lung v1 - L2 - Proximal Basal Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v1 - L2 - Proximal Basal cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Lung v1 - L2 - Proximal Ciliated Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Lung v1 - L2 - Proximal Ciliated cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L1 - Proximal Tubule Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L1 - Proximal Tubule cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L2 - Proximal Tubule Epithelial Segment 1 Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Proximal Tubule Epithelial Segment 1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L2 - Proximal Tubule Epithelial Segment 2 Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Proximal Tubule Epithelial Segment 2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L2 - Proximal Tubule Epithelial Segment 3 Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L2 - Proximal Tubule Epithelial Segment 3 cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L3 - Proximal Tubule Epithelial Segment 1 Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Proximal Tubule Epithelial Segment 1 cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L3 - Proximal Tubule Epithelial Segment 2 Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Proximal Tubule Epithelial Segment 2 cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Human - Kidney - L3 - Proximal Tubule Epithelial Segment 3 Gene Set From HuBMAP Azimuth Cell Type Annotations genes associated with the Human - Kidney - L3 - Proximal Tubule Epithelial Segment 3 cell type from the HuBMAP Azimuth Cell Type Annotations dataset.
Proximal limb bone cell_Bone_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal limb bone cell_Bone_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal limb bud cell_Limb bud_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal limb bud cell_Limb bud_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Enterocyte proximal cell_Intestine_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Enterocyte proximal cell_Intestine_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal cell_Epithelium_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal stem cell_Epithelium_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal stem cell_Epithelium_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal tubular cell_Kidney_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal tubular cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal tubule cell_Kidney_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal tubule cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Early proximal tubule cell_Fetal kidney_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Early proximal tubule cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal segment cell_Fetal kidney_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal segment cell_Fetal kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
General proximal cell_Kidney_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the General proximal cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
S3 proximal cell_Kidney_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the S3 proximal cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
S2 proximal cell_Kidney_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the S2 proximal cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
S1 proximal cell_Kidney_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the S1 proximal cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal tubular cell_Kidney_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal tubular cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal tubule (PT) cell_Kidney_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal tubule (PT) cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal straight tubular cell_Kidney_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal straight tubular cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal convoluted tubular cell_Kidney_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal convoluted tubular cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal tubule cell_Kidney_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal tubule cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal convoluted tubular cell_Kidney_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal convoluted tubular cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal straight tubular cell_Kidney_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal straight tubular cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal tubule-S1 cell_Kidney_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal tubule-S1 cell_Kidney_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
S3 proximal tubule cell_Kidney_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the S3 proximal tubule cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
S1/S2 proximal tubule cell_Kidney_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the S1/S2 proximal tubule cell_Kidney_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal cell_Blood vessel_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal cell_Blood vessel_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal tubular cell_Liver_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal tubular cell_Liver_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal epithelial cell_Lung_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal epithelial cell_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal cell_Prostate_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal cell_Prostate_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal luminal cell_Prostate_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal luminal cell_Prostate_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal S2 cell_Epithelium_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal S2 cell_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal tubular cell_Epithelium_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal tubular cell_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal S3 cell_Epithelium_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal S3 cell_Epithelium_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
Proximal tubular cell_Urine_Human Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Proximal tubular cell_Urine_Human cell type from the CellMarker Gene-Cell Type Associations dataset.
Regucalcin in proximal tubule epithelial kidney cells Gene Set From WikiPathways Pathways 2024 proteins participating in the Regucalcin in proximal tubule epithelial kidney cells pathway from the WikiPathways Pathways 2024 dataset.
Proximal tubule transport Gene Set From WikiPathways Pathways 2024 proteins participating in the Proximal tubule transport pathway from the WikiPathways Pathways 2024 dataset.
16p11 2 proximal deletion syndrome Gene Set From WikiPathways Pathways 2024 proteins participating in the 16p11 2 proximal deletion syndrome pathway from the WikiPathways Pathways 2024 dataset.
Defective SLC4A4 causes renal tubular acidosis, proximal, with ocular abnormalities and mental retardation (pRTA-OA) Gene Set From Reactome Pathways 2024 proteins participating in the Defective SLC4A4 causes renal tubular acidosis, proximal, with ocular abnormalities and mental retardation (pRTA-OA) pathway from the Reactome Pathways 2024 dataset.
proximal/distal pattern formation Gene Set From GO Biological Process Annotations 2025 genes participating in the proximal/distal pattern formation biological process from the curated GO Biological Process Annotations 2025 dataset.
proximal/distal axis specification Gene Set From GO Biological Process Annotations 2025 genes participating in the proximal/distal axis specification biological process from the curated GO Biological Process Annotations 2025 dataset.
metanephric proximal tubule development Gene Set From GO Biological Process Annotations 2025 genes participating in the metanephric proximal tubule development biological process from the curated GO Biological Process Annotations 2025 dataset.
proximal tubule development Gene Set From GO Biological Process Annotations 2025 genes participating in the proximal tubule development biological process from the curated GO Biological Process Annotations 2025 dataset.
proximal dendrite Gene Set From GO Cellular Component Annotations 2025 proteins localized to the proximal dendrite cellular component from the curated GO Cellular Component Annotations 2025 dataset.
proximal neuron projection Gene Set From GO Cellular Component Annotations 2025 proteins localized to the proximal neuron projection cellular component from the curated GO Cellular Component Annotations 2025 dataset.
Proximal symphalangism Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Proximal symphalangism in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Vulvar proximal-type epithelioid sarcoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Vulvar proximal-type epithelioid sarcoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant adult-onset proximal spinal muscular atrophy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant adult-onset proximal spinal muscular atrophy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Renal proximal tubule Gene Set From TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Renal proximal tubule from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset.
Renal proximal tubule Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Renal proximal tubule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Renal proximal tubule cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Renal proximal tubule cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Renal proximal tubule epithelium Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Renal proximal tubule epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Renal proximal tubule epithelial cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Renal proximal tubule epithelial cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Renal proximal tubule epithelium cell line Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Renal proximal tubule epithelium cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Proximal deep inguinal lymph node Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Proximal deep inguinal lymph node in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Proximal portion of axoneme Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Proximal portion of axoneme cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Proximal dendrite Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Proximal dendrite cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Proximal neuron projection Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Proximal neuron projection cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Proximal dendrite Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Proximal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Proximal portion of axoneme Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Proximal portion of axoneme cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Photoreceptor proximal connecting cilium Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Photoreceptor proximal connecting cilium cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Apical proximal dendrite Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Apical proximal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Basal proximal dendrite Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Basal proximal dendrite cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Adult-onset proximal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Adult-onset proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive proximal muscle weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive proximal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proximal symphalangism Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal symphalangism phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proximal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant childhood-onset proximal spinal muscular atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant childhood-onset proximal spinal muscular atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Symphalangism affecting the proximal phalanx of the 4th finger Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Symphalangism affecting the proximal phalanx of the 4th finger phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proximal myopathy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Gastric adenocarcinoma and proximal polyposis of the stomach Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Gastric adenocarcinoma and proximal polyposis of the stomach phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Triangular shaped proximal phalanx of the thumb Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Triangular shaped proximal phalanx of the thumb phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proximal muscle weakness Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal muscle weakness phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proximal lower limb amyotrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal lower limb amyotrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proximal muscle weakness in lower limbs Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal muscle weakness in lower limbs phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive proximal renal tubular acidosis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive proximal renal tubular acidosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proximal amyotrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Proximal amyotrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Proximal colorectal cancer Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Proximal colorectal cancer phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Proximal tubule bicarbonate reclamation Gene Set From KEGG Pathways 2026 proteins participating in the Proximal tubule bicarbonate reclamation pathway from the KEGG Pathways 2026 dataset.

Harmonizome 3.0

HMGN2P31 Gene

HMGB3P5 Gene

HMGN2P19 Gene

HMGN2P18 Gene

HMGN2P12 Gene

HMGN2P11 Gene

HMGN2P10 Gene

HMGN2P17 Gene

HMGN2P16 Gene

HMGN2P15 Gene

HMGN2P14 Gene

HMGN1P9 Gene

HMGN1P4 Gene

HMGN1P5 Gene

HMGN1P6 Gene

HMGN1P7 Gene

HMGN1P1 Gene

HMGN1P2 Gene

LOC100129956 Gene

HMGB3 Gene

HMGB4 Gene

HMGN2P13 Gene

HMGB1P12 Gene

HMGB1P10 Gene

HMGB1P16 Gene

HMGB1P17 Gene

HMGB1P36 Gene

HMGB3P22 Gene

HMGN1P8 Gene

HMGN1P3 Gene

HMGB1P1 Gene

HMGB1P3 Gene

HMGB1P4 Gene

HMGB1P5 Gene

HMGN1P16 Gene

HMGN1P17 Gene

HMGN1P13 Gene

HMGN1P10 Gene

HMGN1P11 Gene

HMGN1P33 Gene

HMGN1P34 Gene

HMGB3P32 Gene

HMGB3P30 Gene

HMGB3P31 Gene

HMGN2P33 Gene

HMGN2P32 Gene

HMGN2P35 Gene

HMGN2P34 Gene

HMGN2P37 Gene

HMGN2P36 Gene

HMGN2P39 Gene

HMGN2P38 Gene

HMGB1P27 Gene

HMGB1P24 Gene

HMGB1P22 Gene

HMGB1P29 Gene

HMGB1P18 Gene

HMGB1P19 Gene

HMGB1P11 Gene

HMGB1P14 Gene

HMGB1P15 Gene

HMGB2 Gene

HMGB1 Gene

HMGN3P1 Gene

HMGB1P45 Gene

HMGA2 Gene

HMGB1P41 Gene

HMGB1P40 Gene

HMGB1P44 Gene

HMGB1P47 Gene

HMGB1P49 Gene

HMGB1P48 Gene

HMGN1P23 Gene

HMGN1P22 Gene

HMGN1P21 Gene

HMGN1P27 Gene

HMGN1P26 Gene

HMGN1P25 Gene

HMGN1P24 Gene