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Ask your administrator if you think this is wrong. ======= TRIM72 ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: TRIM72 * **<color #00a2e8>Official Name</color>**: tripartite motif containing 72 * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=493829|493829]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/Q6ZMU5|Q6ZMU5]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=TRIM72&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20TRIM72|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/613288|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: N/A * **<color #00a2e8>UniProt Summary</color>**: Muscle-specific protein that plays a central role in cell membrane repair by nucleating the assembly of the repair machinery at injury sites. Specifically binds phosphatidylserine. Acts as a sensor of oxidation: upon membrane damage, entry of extracellular oxidative environment results in disulfide bond formation and homooligomerization at the injury site. This oligomerization acts as a nucleation site for recruitment of TRIM72-containing vesicles to the injury site, leading to membrane patch formation. Probably acts upstream of the Ca(2+)-dependent membrane resealing process. Required for transport of DYSF to sites of cell injury during repair patch formation. Regulates membrane budding and exocytosis. May be involved in the regulation of the mobility of KCNB1-containing endocytic vesicles (By similarity). {ECO:0000250}. <button type='primary' size='sm' modal='Pfam_Domains'>Pfam Domains</button> <button type='primary' size='sm' modal='GO_terms'>GO Terms</button> <modal id='Pfam_Domains' size='lg' title='Pfam Domains'> |zf-C3HC4| |zf-B box| |SPRY| </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |negative regulation of insulin-like growth factor receptor signaling pathway| |plasma membrane repair| |negative regulation of myotube differentiation| |regulation of insulin-like growth factor receptor signaling pathway| |ubiquitin conjugating enzyme binding| |negative regulation of insulin receptor signaling pathway| |negative regulation of cellular response to insulin stimulus| |negative regulation of striated muscle cell differentiation| |negative regulation of muscle cell differentiation| |regulation of myotube differentiation| |phosphatidylserine binding| |regulation of insulin receptor signaling pathway| |regulation of cellular response to insulin stimulus| |plasma membrane organization| |sarcolemma| |regulation of striated muscle cell differentiation| |cytoplasmic vesicle membrane| |regulation of muscle cell differentiation| |ubiquitin protein ligase activity| |muscle contraction| |muscle organ development| |muscle system process| |proteasome-mediated ubiquitin-dependent protein catabolic process| |protein homooligomerization| |proteasomal protein catabolic process| |endomembrane system organization| |muscle structure development| |wound healing| |protein complex oligomerization| |ubiquitin-dependent protein catabolic process| |modification-dependent protein catabolic process| |modification-dependent macromolecule catabolic process| |response to wounding| |proteolysis involved in cellular protein catabolic process| |cellular protein catabolic process| |protein catabolic process| |protein ubiquitination| |negative regulation of cell differentiation| |protein modification by small protein conjugation| |exocytosis| |zinc ion binding| |membrane organization| |cellular macromolecule catabolic process| |negative regulation of developmental process| |protein modification by small protein conjugation or removal| |secretion by cell| |export from cell| |macromolecule catabolic process| |organonitrogen compound catabolic process| |secretion| |negative regulation of signal transduction| |proteolysis| |negative regulation of cell communication| |negative regulation of signaling| |protein-containing complex assembly| |negative regulation of response to stimulus| |organic substance catabolic process| |cellular catabolic process| |regulation of cell differentiation| |protein-containing complex subunit organization| |vesicle-mediated transport| |system process| </modal> \\ === CRISPR Data === <button type='primary' size='small' modal='Compound_Hit'>Compound Hit</button> <button type='default' size='small' modal='Most_Correlated_Genes'>Most Correlated Genes in Chemogenomics</button> <button type='primary' size='small' modal='Essential_Avana'>Tissues where Essential in the Avana Dataset (DepMap 20Q1)</button> <modal id='Compound_Hit' size='lg' title='Compound Hit'> ^Screen^Score^ |[[:results:exp243|S-trityl-L-cysteine 0.5μM R05 exp243]]|-2.31| </modal> <modal id='Most_Correlated_Genes' size='lg' title='Most Correlated Genes in Chemogenomics'> No correlation found to any other genes in chemogenomics. </modal> <modal id='Essential_Avana' size='lg' title='Tissues where Essential in the Avana Dataset (DepMap 20Q1)'> Global Fraction of Cell Lines Where Essential: 0/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/26| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| </modal> == Essentiality in NALM6 == * **<color #00a2e8>Essentiality Rank</color>**: 6609 * **<color #00a2e8>Expression level (log2 read counts)</color>**: 4.48 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='TRIM72 Expression in NALM6 Cells: 4.48'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2025/12/10 20:19by 127.0.0.1