======= SNX15 ======= == Gene Information == * **Official Symbol**: SNX15 * **Official Name**: sorting nexin 15 * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=29907|29907]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q9NRS6|Q9NRS6]] * **Interactions**: [[https://thebiogrid.org/search.php?search=SNX15&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20SNX15|Open PubMed]] * **OMIM**: [[https://omim.org/entry/605964|Open OMIM]] == Function Summary == * **Entrez Summary**: This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. Overexpression of this gene results in a decrease in the processing of insulin and hepatocyte growth factor receptors to their mature subunits. This decrease is caused by the mislocalization of furin, the endoprotease responsible for cleavage of insulin and hepatocyte growth factor receptors. This protein is involved in endosomal trafficking from the plasma membrane to recycling endosomes or the trans-Golgi network. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ADP-ribosylation factor-like 2 (ARL2) gene. [provided by RefSeq, Dec 2010]. * **UniProt Summary**: May be involved in several stages of intracellular trafficking. Overexpression of SNX15 disrupts the normal trafficking of proteins from the plasma membrane to recycling endosomes or the TGN. {ECO:0000269|PubMed:11085978}. |MIT| |PX| |phosphatidylinositol binding| |cytoplasmic vesicle membrane| |nucleolus| |intracellular protein transport| |protein transport| |intracellular transport| |peptide transport| |amide transport| |cellular protein localization| |cellular macromolecule localization| |establishment of protein localization| |establishment of localization in cell| |nitrogen compound transport| |membrane| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp64|Nocodazole 0.2μM R02 exp64]]|-1.77| |[[:results:exp262|Alda-1 10μM R06 exp262]]|1.75| |[[:results:exp176|Apcin 50 to 100μM on day4 R04 exp176]]|1.79| |[[:results:exp236|GSK2606414 1μM R05 exp236]]|1.79| |[[:results:exp537|WNT3A 44ng/ml R08 exp537]]|1.8| ^Gene^Correlation^ |[[:human genes:h:hgc6.3|HGC6.3]]|0.536| |[[:human genes:c:copg1|COPG1]]|0.446| |[[:human genes:s:slc6a17|SLC6A17]]|0.436| |[[:human genes:c:cln6|CLN6]]|0.431| |[[:human genes:a:atp6v1c1|ATP6V1C1]]|0.426| |[[:human genes:n:nup153|NUP153]]|0.424| |[[:human genes:d:dtl|DTL]]|0.41| |[[:human genes:a:aamp|AAMP]]|0.407| |[[:human genes:r:rpl30|RPL30]]|0.403| |[[:human genes:c:chaf1a|CHAF1A]]|0.402| |[[:human genes:a:acsf2|ACSF2]]|0.4| 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**: 2370 * **Expression level (log2 read counts)**: 4.43 {{:chemogenomics:nalm6 dist.png?nolink |}}