======= VWA3B =======
== Gene Information ==
* **Official Symbol**: VWA3B
* **Official Name**: von Willebrand factor A domain containing 3B
* **Aliases and Previous Symbols**: N/A
* **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=200403|200403]]
* **UniProt**: [[https://www.uniprot.org/uniprot/Q502W6|Q502W6]]
* **Interactions**: [[https://thebiogrid.org/search.php?search=VWA3B&organism=9606|BioGRID]]
* **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20VWA3B|Open PubMed]]
* **OMIM**: [[https://omim.org/entry/614884|Open OMIM]]
== Function Summary ==
* **Entrez Summary**: This gene encodes an intracellular protein that contains a von Willebrand factor type A domain. Intracellular proteins with VWA domains are thought to function in transcription, DNA repair, ribosomal and membrane transport and the proteasome. Mutations in this gene are associated with Spinocerebellar ataxia, autosomal recessive 22. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2017].
* **UniProt Summary**: N/A
|VWA|
No GO term information is available for this gene.
\\
=== CRISPR Data ===
^Screen^Score^
|[[:results:exp516|Pyrazinamide 100μM R08 exp516]]|-1.99|
^Gene^Correlation^
|[[:human genes:r:rrm1|RRM1]]|0.573|
|[[:human genes:h:hgc6.3|HGC6.3]]|0.436|
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**: 15142
* **Expression level (log2 read counts)**: 0.09
{{:chemogenomics:nalm6 dist.png?nolink |}}