Type | Description |
---|---|
Definition | solute carrier family 26, member 5 |
Date | Results | Publications |
---|---|---|
2020-10-24 14:01:00 | Deletion of exons 17 and 18 in prestin's STAS domain results in loss of function. | 31053797 |
2019-08-31 12:59:00 | Oxidative stress inhibits the expression of Prestin protein, and the transcription mechanism is triggered to compensate for the loss of Prestin protein in HEI-OC1 cells. AP-2delta is one of the important TFs that suppresses transcription of the Prestin gene, and AP-2delta suppression further boosted Prestin mRNA activation under oxidative stress. | 31297132 |
2018-02-10 11:42:00 | response of endogenously expressed prestin in HEI-OC1 cells is different from the response of prestin expressed exogenously in non-auditory cells | 26854618 |
2017-05-27 10:19:00 | The IVS2-2A>G mutation in the Slc26a5 gene is insufficient to cause hearing loss in mice. | 27232762 |
2016-12-24 11:47:00 | Prestin expression imparts susceptibility to 2-hydroxypropyl-beta-cyclodextrin-induced hearing loss. | 26903308 |
Type | IDs |
---|---|
Synonymous | Pres, prestin |
Gene |
UniProtKB-ID:
S26A5_MOUSE,
Q32MT7_MOUSE,
Q32MT6_MOUSE
UniprotKB:
Q99NH7,
Q32MT7,
Q32MT6
UniParc:
UPI00005DC6EA,
UPI0000003AFC,
UPI00005DC6E9
EMBL:
AC125313,
AY024359,
CH466586,
BC108987,
AC113028,
AF529192,
BC108986
Ensembl:
ENSMUSG00000029015
KO:
mmu:80979
|
Nucleutide sequences |
EMBL-CDS:
EDL03187.1,
AAO59381.1,
AAG59999.2,
AAI08987.1,
AAI08988.1
Ensembl_TRS:
ENSMUST00000030878,
ENSMUST00000115176
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000030878,
ENSMUSP00000110830
RefSeq:
NP_109652.3,
NP_001276716.1,
XP_006535881.1,
NP_001276717.1
|
Others |
UniRef100:
UniRef100_Q32MT6,
UniRef100_Q99NH7
UniRef90:
UniRef90_Q9EPH0
UniRef50:
UniRef50_Q9EPH0
UniGene:
Mm.160370
CCDS:
CCDS19109.1
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
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Refseq |
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