Mobility Limitation

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Results for "Mobility Limitation": 192 genes, 36 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*
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.
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.
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.
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.
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.
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.
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.
limitation Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term limitation in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
limitation of neck motion Gene Set From HPO Gene-Disease Associations genes associated with the limitation of neck motion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
flexion limitation of toes Gene Set From HPO Gene-Disease Associations genes associated with the flexion limitation of toes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Flexion Limitation Of Toes Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Flexion Limitation Of Toes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Limitation Of Movement At Ankles Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Limitation Of Movement At Ankles in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.

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