Slc26a4 - solute carrier family 26, member 4 Gene

Also Known as Pds; pendrin

生物種: Mus musculus

遺伝子タイプ: protein coding
遺伝子ID: 23985

Summary

Predicted to enable anion transmembrane transporter activity. Involved in regulation of pH and regulation of protein localization. Located in apical plasma membrane and brush border membrane. Is expressed in central nervous system; cochlear duct; and metanephros. Used to study Pendred Syndrome. 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_011867.4 NP_035997.1 pendrin
Molecular Function GO Annotation Evidence 参考文献 由来
enables chloride:bicarbonate antiporter activity IDA
IDA: Inferred from direct assay
18565999 MGI
enables chloride:bicarbonate antiporter activity IMP
IMP: Inferred from mutant phenotype
11274445 MGI
enables protein binding IPI
IPI: Inferred from physical interaction
35601831 MGI
Biological Process GO Annotation Evidence 参考文献 由来
involved in regulation of pH IMP
IMP: Inferred from mutant phenotype
16144965 MGI
involved in regulation of protein localization IMP
IMP: Inferred from mutant phenotype
16144965 MGI
Cellular Component GO Annotation Evidence 参考文献 由来
located in apical plasma membrane IDA
IDA: Inferred from direct assay
11274445 MGI
located in brush border membrane IDA
IDA: Inferred from direct assay
11459928 MGI
located in membrane IDA
IDA: Inferred from direct assay
17409310 MGI
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

  • sodium-independent chloride/iodide transporter

Orthologs Information

生物種 Symbol 由来 ID
Homo sapiens Slc26a4 NCBI NCBI:5172