======= COG8 ======= == Gene Information == * **Official Symbol**: COG8 * **Official Name**: component of oligomeric golgi complex 8 * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=84342|84342]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q96MW5|Q96MW5]] * **Interactions**: [[https://thebiogrid.org/search.php?search=COG8&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20COG8|Open PubMed]] * **OMIM**: [[https://omim.org/entry/606979|Open OMIM]] == Function Summary == * **Entrez Summary**: This gene encodes a protein that is a component of the conserved oligomeric Golgi (COG) complex, a multiprotein complex that plays a structural role in the Golgi apparatus, and is involved in intracellular membrane trafficking and glycoprotein modification. Mutations in this gene cause congenital disorder of glycosylation, type IIh, a disease that is characterized by under-glycosylated serum proteins, and whose symptoms include severe psychomotor retardation, failure to thrive, seizures, and dairy and wheat product intolerance. [provided by RefSeq, Jul 2008]. * **UniProt Summary**: Required for normal Golgi function. {ECO:0000250}. |Dor1| |Golgi transport complex| |intra-Golgi vesicle-mediated transport| |trans-Golgi network membrane| |endoplasmic reticulum to Golgi vesicle-mediated transport| |Golgi vesicle transport| |Golgi membrane| |Golgi apparatus| |protein transport| |intracellular transport| |peptide transport| |amide transport| |establishment of protein localization| |establishment of localization in cell| |nitrogen compound transport| |vesicle-mediated transport| |membrane| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp52|Ribavirin 10μM R01 exp52]]|-1.96| |[[:results:exp134|MS023 2μM R03 exp134]]|-1.73| ^Gene^Correlation^ |[[:human genes:c:cog2|COG2]]|0.486| |[[:human genes:p:prim1|PRIM1]]|0.473| |[[:human genes:c:cog1|COG1]]|0.452| |[[:human genes:c:cog7|COG7]]|0.445| |[[:human genes:c:cog4|COG4]]|0.444| |[[:human genes:c:cog3|COG3]]|0.403| 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|1/28| |blood|0/28| |bone|1/26| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|1/21| |liver|0/20| |lung|1/75| |lymphocyte|0/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|2/15| |prostate|0/1| |skin|1/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|1/22| |urinary tract|0/29| |uterus|0/5| == Essentiality in NALM6 == * **Essentiality Rank**: 2521 * **Expression level (log2 read counts)**: 6.48 {{:chemogenomics:nalm6 dist.png?nolink |}}