SLC26A5 (solute carrier family 26 member 5)

2010-03-01  

Identity

HGNC
LOCATION
7q22.1
LOCUSID
ALIAS
DFNB61,PRES
FUSION GENES

Other Information

Locus ID:

NCBI: 375611
MIM: 604943
HGNC: 9359
Ensembl: ENSG00000170615

Variants:

dbSNP: 375611
ClinVar: 375611
TCGA: ENSG00000170615
COSMIC: SLC26A5

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000170615ENST00000306312P58743
ENSG00000170615ENST00000339444P58743
ENSG00000170615ENST00000354356Q7Z7F4
ENSG00000170615ENST00000356767P58743
ENSG00000170615ENST00000393723P58743
ENSG00000170615ENST00000393727Q7Z7F4
ENSG00000170615ENST00000393729E9PCM2
ENSG00000170615ENST00000393730P58743
ENSG00000170615ENST00000393735P58743
ENSG00000170615ENST00000423416Q496J3
ENSG00000170615ENST00000432958P58743
ENSG00000170615ENST00000445809F8WD50
ENSG00000170615ENST00000454864Q496J0
ENSG00000170615ENST00000456463F8WDL4

Expression (GTEx)

0
1
2
3
4

References

Pubmed IDYearTitleCitations
382374832024Evaluation of inner ear damage by mastoid drilling with measurement of serum prestin (SLC26A5) levels.1
384319072024The pathogenic roles of the p.R130S prestin variant in DFNB61 hearing loss.1
384740072024Functional Studies of Deafness-Associated Pendrin and Prestin Variants.1
382374832024Evaluation of inner ear damage by mastoid drilling with measurement of serum prestin (SLC26A5) levels.1
384319072024The pathogenic roles of the p.R130S prestin variant in DFNB61 hearing loss.1
384740072024Functional Studies of Deafness-Associated Pendrin and Prestin Variants.1
350641952022Noise exposure levels predict blood levels of the inner ear protein prestin.9
350641952022Noise exposure levels predict blood levels of the inner ear protein prestin.9
342734092021Prestin and otolin-1 proteins in the hearing loss of adults chronically exposed to lead.3
343906432021Molecular mechanism of prestin electromotive signal amplification.39
342734092021Prestin and otolin-1 proteins in the hearing loss of adults chronically exposed to lead.3
343906432021Molecular mechanism of prestin electromotive signal amplification.39
310537972019Deletion of exons 17 and 18 in prestin's STAS domain results in loss of function.3
310537972019Deletion of exons 17 and 18 in prestin's STAS domain results in loss of function.3
297770562018The extracellular loop of pendrin and prestin modulates their voltage-sensing property.10

Citation

Dessen P

SLC26A5 (solute carrier family 26 member 5)

Atlas Genet Cytogenet Oncol Haematol. 2010-03-01

Online version: http://atlasgeneticsoncology.org/gene/51370/slc26a5