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115111 SLC26A7

115111

SLC26A7

solute carrier family 26 member 7

protein-coding

Homo sapiens

基因描述

Type Description
Definition solute carrier family 26 member 7

研究结论

Date Results Publications
2020-12-19 13:39:00 SLC26A7 constitutes the thiocyanate-selective anion conductance of the basolateral membrane of the retinal pigment epithelium. 32726161
2020-01-11 10:39:00 Study reports homozygous truncating mutations in SLC26A7 in 6 unrelated families with goitrous congenital hypothyroidism and shows that goitrous hypothyroidism also occurs in Slc26a7-null mice. 30333321
2018-12-22 10:25:00 SLC26A7 mutations appear to be associated with thyroid dyshormonogenesis. 29546359
2010-01-21 00:00:00 the molecular cloning from human HEVEC of a 2.9-kb cDNA encoding SLC26A7, a novel member of the SLC26 (solute carrier 26) sulfate/anion exchanger family 11829495
2010-01-21 00:00:00 The trafficking to the cell surface suggests novel functional upregulation of SLC26A7 in states that are associated with hypokalemia or increased medullary tonicity. 16524946

名称对应

Type IDs
Synonymous SUT2
Gene
UniProtKB-ID: S26A7_HUMAN, A0A087WZI7_HUMAN
UniprotKB: Q8TE54, A0A087WZI7
UniParc: UPI00038F2706, UPI0000046B1E, UPI0000046B1C
EMBL: BC113866, BC114474, AF331521, AJ413230, AC087847, AC104967, BC094730, AJ413229, AJ413228, AC104966, KC877270, CH471060
Ensembl: ENSG00000147606
KO: hsa:115111
Nucleutide sequences
EMBL-CDS: CAC88372.1, AAH94730.1, AAI13867.1, AAK95665.1, CAC88371.1, CAC88370.1, EAW91680.1, EAW91679.1, AAI14475.1
Ensembl_TRS: ENST00000276609, ENST00000309536, ENST00000523719, ENST00000617233, ENST00000617078
Protein sequencees
Ensembl_PRO: ENSP00000428849, ENSP00000482549, ENSP00000309504, ENSP00000276609, ENSP00000482686
RefSeq: NP_439897.1, NP_001269285.1, NP_599028.1, NP_001269286.1
Others
UniRef100: UniRef100_Q8TE54
UniRef90: UniRef90_Q8TE54
UniRef50: UniRef50_Q8TE54
UniGene: Hs.354013
CCDS: CCDS6254.1, CCDS6255.1

全选

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