======= VIPAS39 ======= == Gene Information == * **Official Symbol**: VIPAS39 * **Official Name**: VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=63894|63894]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q9H9C1|Q9H9C1]] * **Interactions**: [[https://thebiogrid.org/search.php?search=VIPAS39&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20VIPAS39|Open PubMed]] * **OMIM**: [[https://omim.org/entry/613401|Open OMIM]] == Function Summary == * **Entrez Summary**: This gene encodes a protein involved in the sorting of lysosomal proteins. Mutations in this gene are associated with ARCS2 (arthrogryposis, renal dysfunction, and cholestasis-2). Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jul 2010]. * **UniProt Summary**: Proposed to be involved in endosomal maturation implicating in part VPS33B. In epithelial cells, the VPS33B:VIPAS39 complex may play a role in the apical RAB11A- dependent recycling pathway and in the maintenance of the apical- basolateral polarity (PubMed:20190753). May play a role in lysosomal trafficking, probably via association with the core HOPS complex in a discrete population of endosomes; the functions seems to be indepenedent of VPS33B (PubMed:19109425). May play a role in vesicular trafficking during spermatogenesis (By similarity). May be involved in direct or indirect transcriptional regulation of E- cadherin (By similarity). {ECO:0000250|UniProtKB:Q23288, ECO:0000269|PubMed:19109425, ECO:0000269|PubMed:20190753}. |Vps16 C| |Golgin A5| |peptidyl-lysine hydroxylation| |HOPS complex| |protein hydroxylation| |autophagosome maturation| |collagen fibril organization| |endosome to lysosome transport| |collagen metabolic process| |lysosomal transport| |recycling endosome| |late endosome| |vacuolar transport| |macroautophagy| |protein-containing complex disassembly| |early endosome| |autophagy| |process utilizing autophagic mechanism| |protein-containing complex binding| |peptidyl-lysine modification| |extracellular matrix organization| |post-translational protein modification| |extracellular structure organization| |cellular component disassembly| |supramolecular fiber organization| |spermatogenesis| |male gamete generation| |gamete generation| |multicellular organismal reproductive process| |sexual reproduction| |multicellular organism reproduction| |peptidyl-amino acid modification| |Golgi apparatus| |intracellular protein transport| |multi-organism reproductive process| |reproductive process| |reproduction| |protein transport| |intracellular transport| |peptide transport| |amide transport| |cellular protein localization| |cellular macromolecule localization| |establishment of protein localization| |cellular catabolic process| |establishment of localization in cell| |nitrogen compound transport| |protein-containing complex subunit organization| |vesicle-mediated transport| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp146|Quinacrine 2.5μM R03 exp146]]|-1.96| |[[:results:exp75|MK-1775 0.32μM R02 exp75]]|-1.79| |[[:results:exp156|UNC2400 2μM R03 exp156]]|-1.7| 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**: 14332 * **Expression level (log2 read counts)**: 4.56 {{:chemogenomics:nalm6 dist.png?nolink |}}