SLC26A4

Gene Information
  • Official Symbol: SLC26A4
  • Official Name: solute carrier family 26 member 4
  • Aliases and Previous Symbols: N/A
  • Entrez ID: 5172
  • UniProt: O43511
  • Interactions: BioGRID
  • PubMed articles: Open PubMed
  • OMIM: 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}.

Pfam Domains GO Terms


CRISPR Data

Compound Hit Most Correlated Genes in Chemogenomics Tissues where Essential in the Avana Dataset (DepMap 20Q1)

Essentiality in NALM6
  • Essentiality Rank: 14929
  • Expression level (log2 read counts): 1.77

Expression Distribution

  • Last modified: 2025/12/10 20:19
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