======= SLC7A14 =======
== Gene Information ==
* **Official Symbol**: SLC7A14
* **Official Name**: solute carrier family 7 member 14
* **Aliases and Previous Symbols**: N/A
* **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=57709|57709]]
* **UniProt**: [[https://www.uniprot.org/uniprot/Q8TBB6|Q8TBB6]]
* **Interactions**: [[https://thebiogrid.org/search.php?search=SLC7A14&organism=9606|BioGRID]]
* **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20SLC7A14|Open PubMed]]
* **OMIM**: [[https://omim.org/entry/615720|Open OMIM]]
== Function Summary ==
* **Entrez Summary**: This gene is predicted to encode a glycosylated, cationic amino acid transporter protein with 14 transmembrane domains. This gene is primarily expressed in skin fibroblasts, neural tissue, and primary endothelial cells and its protein is predicted to mediate lysosomal uptake of cationic amino acids. Mutations in this gene are associated with autosomal recessive retinitis pigmentosa. In mice, this gene is expressed in the photoreceptor layer of the retina where its expression increases over the course of retinal development and persists in the mature retina. [provided by RefSeq, Apr 2014].
* **UniProt Summary**: May be involved in arginine transport. {ECO:0000269|PubMed:22787143, ECO:0000269|PubMed:24670872}.
|AA permease|
|transmembrane transporter activity|
|negative regulation of phosphatase activity|
|negative regulation of dephosphorylation|
|amino acid transport|
|regulation of phosphatase activity|
|regulation of dephosphorylation|
|organic acid transport|
|carboxylic acid transport|
|lysosomal membrane|
|negative regulation of hydrolase activity|
|organic anion transport|
|negative regulation of phosphate metabolic process|
|negative regulation of phosphorus metabolic process|
|anion transport|
|negative regulation of catalytic activity|
|negative regulation of molecular function|
|transmembrane transport|
|regulation of hydrolase activity|
|ion transport|
|regulation of phosphate metabolic process|
|regulation of phosphorus metabolic process|
|nitrogen compound transport|
\\
=== CRISPR Data ===
No hits were found.
No correlation found to any other genes in chemogenomics.
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**: 11786
* **Expression level (log2 read counts)**: 3.62
{{:chemogenomics:nalm6 dist.png?nolink |}}