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> Protein (NX_P58743)
Protein (NX_P58743)
Protein
Gene SymbolSLC26A5 to neXtProt (NX_P58743)
DescriptionPrestin
Chromosome7
Location7q22.1 (102993177 ~ 103086624) to Ensembl
Sequene Features : Isoforms 6, Variants 125, PTMsto neXtProt Sequence Features
Gene
Ontologies
GO: Biological Process GO: Mulecular Function GO: Cellular Component
.regulation of membrane potential
.regulation of cell shape
.sensory perception of sound
.secondary active sulfate transmembrane transporter activity .lateral plasma membrane
.basolateral plasma membrane
.integral component of membrane
Proteomic Evidences
ReleaseProtein EvidencePrAbIsoformsVariantsPTMs
2015-01-01transcript level
6 125 2
2014-09-19transcript level
6 85 2
2014-05-27transcript level
6 84 2
2014-02-25transcript level
6 82 2
2013-12-09transcript level
6 74 2
2013-11-01transcript level
6 69 2
2013-09-12transcript level
6 69 2
2013-08-17transcript level
6 69 2
2013-07-15transcript level
5 51 2
2013-06-11transcript level
5 51 2
2013-02-12transcript level
5 22 10
2012-12-20transcript level
5 21 10
2012-10-30transcript level
5 23 10
2012-10-07transcript level
5 23 2
2012-08-24transcript level
5 10 2
2012-07-28transcript level
5 10 2
2012-06-08transcript level
5 10 2
2012-05-07transcript level
5 10 2
2012-04-10transcript level
4 10 2
2012-01-13transcript level
4 4 2
2011-12-20transcript level
4 4 2
2011-11-11transcript level
4 4 2
2011-08-23transcript level
4 4 2
Protein Isoforms
Isoform Ac UGSMw (Da)
NX_P58743-1
0 30 0 81211.4083
NX_P58743-2
1 27 0 74795.3
NX_P58743-3
1 20 0 56420.9304
NX_P58743-4
1 14 0 36924.5321
NX_P58743-5
0 28 0 77529.4367
NX_P58743-6
1 27 0 77758.5423
: Uniquely mapped peptide
: Gene-specific peptide
: Shared peptide
EST expression level of Protein Coding Gene (ref. NCBI UniGene EST)
Body Sites
TissuesTPM*
brain2
stomach10
Health State
TissuesTPM*
non-neoplasia10
Developmental Stage
TissuesTPM*
adult1
TPM*: Transcripts per million; transcript expression level measured by expression sequence tags.
Disease
No.Disease DescriptionRef.
1(*604943, gene) Solute carrier family 26, member 5; SLC26A5OMIM
2(#613865, phenotype) Deafness, autosomal recessive 61; DFNB61OMIM


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