======= 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 |}}