======= SLC26A4 =======
== Gene Information ==
* **Official Symbol**: SLC26A4
* **Official Name**: solute carrier family 26 member 4
* **Aliases and Previous Symbols**: N/A
* **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=5172|5172]]
* **UniProt**: [[https://www.uniprot.org/uniprot/O43511|O43511]]
* **Interactions**: [[https://thebiogrid.org/search.php?search=SLC26A4&organism=9606|BioGRID]]
* **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20SLC26A4|Open PubMed]]
* **OMIM**: [[https://omim.org/entry/605646|Open OMIM]]
== Function Summary ==
* **Entrez Summary**: Mutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. [provided by RefSeq, Jul 2008].
* **UniProt Summary**: Sodium-independent transporter of chloride and iodide. {ECO:0000269|PubMed:10192399}.
|Sulfate transp|
|STAS|
|iodide transmembrane transporter activity|
|iodide transport|
|oxalate transmembrane transporter activity|
|secondary active sulfate transmembrane transporter activity|
|oxalate transport|
|bicarbonate transmembrane transporter activity|
|sulfate transmembrane transporter activity|
|chloride transmembrane transporter activity|
|sulfate transmembrane transport|
|sulfate transport|
|anion:anion antiporter activity|
|bicarbonate transport|
|sulfur compound transport|
|brush border membrane|
|dicarboxylic acid transport|
|chloride transmembrane transport|
|regulation of pH|
|chloride transport|
|inorganic anion transmembrane transport|
|monovalent inorganic cation homeostasis|
|sensory perception of sound|
|inorganic anion transport|
|sensory perception of mechanical stimulus|
|anion transmembrane transport|
|carboxylic acid transport|
|organic acid transport|
|apical plasma membrane|
|organic anion transport|
|anion transport|
|inorganic ion transmembrane transport|
|cation homeostasis|
|inorganic ion homeostasis|
|ion homeostasis|
|ion transmembrane transport|
|sensory perception|
|regulation of protein localization|
|chemical homeostasis|
|transmembrane transport|
|ion transport|
|nervous system process|
|integral component of plasma membrane|
|homeostatic process|
|system process|
\\
=== CRISPR Data ===
^Screen^Score^
|[[:results:exp331|A-769662 20μM R07 exp331]]|1.73|
|[[:results:exp422|Wiskostatin 3μM R07 exp422]]|1.93|
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**: 14929
* **Expression level (log2 read counts)**: 1.77
{{:chemogenomics:nalm6 dist.png?nolink |}}