1. Gene
  2. Slc26a4 - solute carrier family 26 member 4 Gene

Slc26a4 - solute carrier family 26 member 4 Gene

Rattus norvegicus

Also known as Pds

Gene ID: 29440 | Gene type: protein coding

About Slc26a4

Summary

Enables chloride transmembrane transporter activity and iodide transmembrane transporter activity. Involved in inorganic anion transport. Located in apical plasma membrane. Human ortholog(s) of this gene implicated in Pendred Syndrome; autosomal recessive nonsyndromic deafness 4; and goiter. Orthologous to human SLC26A4 (solute carrier family 26 member 4). [provided by Alliance of Genome Resources, Apr 2022]

Slc26a4 Products(1)

mRNA Protein Name
NM_019214.1 NP_062087.1 pendrin
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables chloride transmembrane transporter activity IDA
IDA: Inferred from direct assay
12107249 RGD
enables chloride:bicarbonate antiporter activity IDA
IDA: Inferred from direct assay
11208611 RGD
enables iodide transmembrane transporter activity IDA
IDA: Inferred from direct assay
12107249 RGD
Biological Process GO Annotation Evidence Reference Source
involved in inorganic anion transport IDA
IDA: Inferred from direct assay
12107249 RGD
Cellular Component GO Annotation Evidence Reference Source
located in apical plasma membrane IDA
IDA: Inferred from direct assay
11208611 RGD
located in plasma membrane IDA
IDA: Inferred from direct assay
26791486 RGD
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

pendrin

Pendred syndrome homolog

sodium-independent chloride/iodide transporter

solute carrier family 26 (anion exchanger), member 4

Orthologs Information

Species Symbol Source ID
Homo sapiens Slc26a4 NCBI NCBI:5172