======= C20orf194 =======
== Gene Information ==
* **Official Symbol**: C20orf194
* **Official Name**: chromosome 20 open reading frame 194
* **Aliases and Previous Symbols**: N/A
* **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=25943|25943]]
* **UniProt**: [[https://www.uniprot.org/uniprot/Q5TEA3|Q5TEA3]]
* **Interactions**: [[https://thebiogrid.org/search.php?search=C20orf194&organism=9606|BioGRID]]
* **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20C20orf194|Open PubMed]]
* **OMIM**: N/A
== Function Summary ==
* **Entrez Summary**: This gene encodes an uncharacterized protein with a C-terminal coiled-coil region. The gene is located on chromosome 20p13 in a 1.8 Mb region linked to a spinocerebellar ataxia phenotype, but this gene does not appear to be a disease candidate. [provided by RefSeq, Dec 2011].
* **UniProt Summary**: May act as an effector for ARL3.
No Pfam Domain information is available for this gene.
|cellular component|
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=== CRISPR Data ===
^Screen^Score^
|[[:results:exp256|HMS-I1 10μM R06 exp256]]|-1.79|
|[[:results:exp459|Bleomycin 5μM R08 exp459]]|1.86|
^Gene^Correlation^
|[[:human genes:h:hgc6.3|HGC6.3]]|0.676|
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**: 10951
* **Expression level (log2 read counts)**: 4.56
{{:chemogenomics:nalm6 dist.png?nolink |}}