======= TRIM63 =======
== Gene Information ==
* **Official Symbol**: TRIM63
* **Official Name**: tripartite motif containing 63
* **Aliases and Previous Symbols**: N/A
* **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=84676|84676]]
* **UniProt**: [[https://www.uniprot.org/uniprot/Q969Q1|Q969Q1]]
* **Interactions**: [[https://thebiogrid.org/search.php?search=TRIM63&organism=9606|BioGRID]]
* **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20TRIM63|Open PubMed]]
* **OMIM**: [[https://omim.org/entry/606131|Open OMIM]]
== Function Summary ==
* **Entrez Summary**: This gene encodes a member of the RING zinc finger protein family found in striated muscle and iris. The product of this gene is an E3 ubiquitin ligase that localizes to the Z-line and M-line lattices of myofibrils. This protein plays an important role in the atrophy of skeletal and cardiac muscle and is required for the degradation of myosin heavy chain proteins, myosin light chain, myosin binding protein, and for muscle-type creatine kinase. [provided by RefSeq, Feb 2012].
* **UniProt Summary**: E3 ubiquitin ligase. Mediates the ubiquitination and subsequent proteasomal degradation of CKM, GMEB1 and HIBADH. Regulates the proteasomal degradation of muscle proteins under amino acid starvation, where muscle protein is catabolized to provide other organs with amino acids. Inhibits de novo skeletal muscle protein synthesis under amino acid starvation. Regulates proteasomal degradation of cardiac troponin I/TNNI3 and probably of other sarcomeric-associated proteins. May play a role in striated muscle atrophy and hypertrophy by regulating an anti- hypertrophic PKC-mediated signaling pathway. May regulate the organization of myofibrils through TTN in muscle cells. {ECO:0000269|PubMed:11927605, ECO:0000269|PubMed:18222470}.
|zf-B box|
|zf-C3HC4|
|response to electrical stimulus involved in regulation of muscle adaptation|
|skeletal muscle atrophy|
|striated muscle atrophy|
|muscle atrophy|
|skeletal muscle adaptation|
|titin binding|
|response to stimulus involved in regulation of muscle adaptation|
|negative regulation of cardiac muscle hypertrophy|
|striated muscle adaptation|
|M band|
|negative regulation of muscle hypertrophy|
|muscle adaptation|
|response to electrical stimulus|
|regulation of cardiac muscle hypertrophy|
|regulation of muscle hypertrophy|
|regulation of muscle adaptation|
|Z disc|
|response to glucocorticoid|
|response to corticosteroid|
|response to interleukin-1|
|regulation of muscle system process|
|ubiquitin-protein transferase activity|
|muscle contraction|
|muscle system process|
|microtubule|
|response to steroid hormone|
|regulation of system process|
|protein ubiquitination|
|protein modification by small protein conjugation|
|zinc ion binding|
|response to lipid|
|response to hormone|
|response to organic cyclic compound|
|protein modification by small protein conjugation or removal|
|response to cytokine|
|response to abiotic stimulus|
|negative regulation of multicellular organismal process|
|response to endogenous stimulus|
|system process|
\\
=== CRISPR Data ===
^Screen^Score^
|[[:results:exp60|Vinblastine 0.002μM R01 exp60]]|1.81|
No correlation found to any other genes in chemogenomics.
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|
== Essentiality in NALM6 ==
* **Essentiality Rank**: 12843
* **Expression level (log2 read counts)**: -6.6
{{:chemogenomics:nalm6 dist.png?nolink |}}