SLC26A4

GENE INFORMATION

? »

Gene name

SLC26A4 (HGNC Symbol)

Synonyms

DFNB4, PDS

Description

Solute carrier family 26 (anion exchanger), member 4 (HGNC Symbol)

Entrez gene 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]

Chromosome

7

Cytoband

q22.3

Chromosome location (bp)

107660635 - 107717809

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000091137 (version 78.38)

Entrez gene

5172

UniProt

O43511 (UniProt - Evidence at protein level)

neXtProt

NX_O43511

Antibodypedia

SLC26A4 antibodies
 

PROTEIN VIEW

? »
 
 
 
SLC26A4-001
 
SLC26A4-002
 
 
 
 
 

PROTEIN INFORMATION

? »

Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

SLC26A4-001 ENSP00000265715
ENST00000265715
O43511
Show all »
Show » Show » 780 85.7 No >9
SLC26A4-002 ENSP00000394760
ENST00000440056
C9JQG1
Show all »
Show » 131 14.7 No 2