SLC26A4

GENE INFORMATION

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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)

107301080 - 107358254

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000091137 (version 75.37)

Entrez gene

5172

UniProt

O43511 (UniProt - Evidence at protein level)

neXtProt

NX_O43511

Antibodypedia

SLC26A4 antibodies
 

PROTEIN VIEW

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SLC26A4-001
 
SLC26A4-002
 
SLC26A4-201
 
SLC26A4-202
 
SLC26A4-203
 
 
 
 
 

PROTEIN INFORMATION

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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 » Show » 131 14.7 No 2
SLC26A4-201 ENSP00000439743
ENST00000541474
F5H104
Show all »
Show » 341 38.4 No 1
SLC26A4-202 ENSP00000441209
ENST00000543100
B7Z266
Show all »
Show » Show » 349 39.3 No 1
SLC26A4-203 ENSP00000437427
ENST00000544569
B7Z6M6
Show all »
Show » Show » 367 41 No 3