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Ask your administrator if you think this is wrong. ======= SYVN1 ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: SYVN1 * **<color #00a2e8>Official Name</color>**: synoviolin 1 * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=84447|84447]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/Q86TM6|Q86TM6]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=SYVN1&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20SYVN1|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/608046|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: This gene encodes a protein involved in endoplasmic reticulum (ER)-associated degradation. The encoded protein removes unfolded proteins, accumulated during ER stress, by retrograde transport to the cytosol from the ER. This protein also uses the ubiquitin-proteasome system for additional degradation of unfolded proteins. Sequence analysis identified two transcript variants that encode different isoforms. [provided by RefSeq, May 2011]. * **<color #00a2e8>UniProt Summary</color>**: Acts as an E3 ubiquitin-protein ligase which accepts ubiquitin specifically from endoplasmic reticulum-associated UBC7 E2 ligase and transfers it to substrates, promoting their degradation (PubMed:12459480, PubMed:12646171, PubMed:12975321, PubMed:14593114, PubMed:16289116, PubMed:16847254, PubMed:17059562, PubMed:17141218, PubMed:17170702, PubMed:22607976, PubMed:26471130). Component of the endoplasmic reticulum quality control (ERQC) system also called ER-associated degradation (ERAD) involved in ubiquitin-dependent degradation of misfolded endoplasmic reticulum proteins (PubMed:12459480, PubMed:12646171, PubMed:12975321, PubMed:14593114, PubMed:16289116, PubMed:16847254, PubMed:17059562, PubMed:17141218, PubMed:17170702, PubMed:22607976, PubMed:26471130). Also promotes the degradation of normal but naturally short-lived proteins such as SGK. Protects cells from ER stress-induced apoptosis. Protects neurons from apoptosis induced by polyglutamine-expanded huntingtin (HTT) or unfolded GPR37 by promoting their degradation (PubMed:17141218). Sequesters p53/TP53 in the cytoplasm and promotes its degradation, thereby negatively regulating its biological function in transcription, cell cycle regulation and apoptosis (PubMed:17170702). Mediates the ubiquitination and subsequent degradation of cytoplasmic NFE2L1 (By similarity). {ECO:0000250|UniProtKB:Q9DBY1, ECO:0000269|PubMed:12459480, ECO:0000269|PubMed:12646171, ECO:0000269|PubMed:12975321, ECO:0000269|PubMed:14593114, ECO:0000269|PubMed:16289116, ECO:0000269|PubMed:16847254, ECO:0000269|PubMed:17059562, ECO:0000269|PubMed:17141218, ECO:0000269|PubMed:17170702, ECO:0000269|PubMed:22607976, ECO:0000269|PubMed:26471130}. <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-rbx1| </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |Hrd1p ubiquitin ligase complex| |Hrd1p ubiquitin ligase ERAD-L complex| |Derlin-1 retrotranslocation complex| |endoplasmic reticulum mannose trimming| |ubiquitin-specific protease binding| |endoplasmic reticulum to cytosol transport| |retrograde protein transport, ER to cytosol| |negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway| |protein demannosylation| |protein alpha-1,2-demannosylation| |endoplasmic reticulum quality control compartment| |protein exit from endoplasmic reticulum| |smooth endoplasmic reticulum| |protein deglycosylation| |regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway| |protein N-linked glycosylation via asparagine| |peptidyl-asparagine modification| |negative regulation of response to endoplasmic reticulum stress| |protein K48-linked ubiquitination| |IRE1-mediated unfolded protein response| |ubiquitin-dependent ERAD pathway| |protein N-linked glycosylation| |ATPase binding| |regulation of response to endoplasmic reticulum stress| |ERAD pathway| |negative regulation of intrinsic apoptotic signaling pathway| |chaperone binding| |endoplasmic reticulum unfolded protein response| |integral component of endoplasmic reticulum membrane| |cellular response to unfolded protein| |unfolded protein binding| |cellular response to topologically incorrect protein| |regulation of intrinsic apoptotic signaling pathway| |response to unfolded protein| |protein stabilization| |response to topologically incorrect protein| |ubiquitin protein ligase activity| |negative regulation of apoptotic signaling pathway| |protein glycosylation| |response to endoplasmic reticulum stress| |macromolecule glycosylation| |glycosylation| |regulation of protein stability| |protein polyubiquitination| |glycoprotein biosynthetic process| |proteasome-mediated ubiquitin-dependent protein catabolic process| |proteasomal protein catabolic process| |glycoprotein metabolic process| |regulation of apoptotic signaling pathway| |negative regulation of intracellular signal transduction| |ubiquitin-dependent protein catabolic process| |modification-dependent protein catabolic process| |modification-dependent macromolecule catabolic process| |proteolysis involved in cellular protein catabolic process| |carbohydrate derivative biosynthetic process| |cellular protein catabolic process| |protein catabolic process| |protein ubiquitination| |regulation of cellular response to stress| |protein modification by small protein conjugation| |peptidyl-amino acid modification| |negative regulation of apoptotic process| |cellular macromolecule catabolic process| |negative regulation of programmed cell death| |endoplasmic reticulum membrane| |protein modification by small protein conjugation or removal| |intracellular protein transport| |negative regulation of cell death| |response to organonitrogen compound| |endoplasmic reticulum| |carbohydrate derivative metabolic process| |macromolecule catabolic process| |organonitrogen compound catabolic process| |response to nitrogen compound| |negative regulation of signal transduction| |proteolysis| |negative regulation of cell communication| |negative regulation of signaling| |organonitrogen compound biosynthetic process| |regulation of response to stress| |protein transport| |intracellular transport| |peptide transport| |regulation of apoptotic process| |regulation of programmed cell death| |amide transport| |cellular protein localization| |cellular macromolecule localization| |establishment of protein localization| |negative regulation of response to stimulus| |regulation of cell death| |cellular response to stress| |cellular macromolecule biosynthetic process| |macromolecule biosynthetic process| |organic substance catabolic process| |cellular catabolic process| |regulation of intracellular signal transduction| |establishment of localization in cell| |nitrogen compound transport| |membrane| </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:exp320|ABT-702 5μM plus CoCl2 18μM R07 exp320]]|-3.18| |[[:results:exp504|MK2206 4μM R08 exp504]]|-2.1| |[[:results:exp94|Nocodazole 0.1μM R03 exp94]]|-2.04| |[[:results:exp26|Oligomycin-A 20μM R00 exp26]]|-1.94| |[[:results:exp435|JQ1 0.8μM R08 exp435]]|-1.93| |[[:results:exp215|Colchicine 0.009μM R05 exp215]]|-1.75| |[[:results:exp346|CoCl2 18μM R07 exp346]]|-1.72| |[[:results:exp126|GSK461364A 0.1μM R03 exp126]]|-1.71| |[[:results:exp352|Dexamethasone 0.006 to 0.015μM on day4 R07 exp352]]|1.73| |[[:results:exp426|FBS-Wisent 0.1 R07 exp426]]|1.77| |[[:results:exp421|VHL-ligand-1 20μM R07 exp421]]|1.78| |[[:results:exp42|BI-6727 0.001μM R01 exp42]]|1.79| |[[:results:exp461|BS-181 20μM R08 exp461]]|1.79| |[[:results:exp285|GW501516 25μM R06 exp285]]|1.81| |[[:results:exp125|GSK461364A 0.005μM R03 exp125]]|1.93| |[[:results:exp243|S-trityl-L-cysteine 0.5μM R05 exp243]]|1.93| |[[:results:exp481|Ethambutol 25μM R08 exp481]]|1.95| |[[:results:exp414|Tozasertib 0.1μM R07 exp414]]|1.98| |[[:results:exp103|Taxol 0.004μM R03 exp103]]|2.06| |[[:results:exp95|BI-2536 0.0042μM R03 exp95]]|2.12| |[[:results:exp128|GSK591 2.6μM R03 exp128]]|2.12| |[[:results:exp142|OICR-9429 10μM R03 exp142]]|2.21| |[[:results:exp169|BH1 1μM R04 exp169]]|3.07| </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: 11/739 ^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|1/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|0/21| |liver|0/20| |lung|1/75| |lymphocyte|0/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|6/15| |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>**: 504 * **<color #00a2e8>Expression level (log2 read counts)</color>**: 8.38 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='SYVN1 Expression in NALM6 Cells: 8.38'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2026/01/07 22:37by 127.0.0.1