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160728 SLC5A8

160728

SLC5A8

solute carrier family 5 member 8

protein-coding

Homo sapiens

基因描述

Type Description
Definition solute carrier family 5 member 8

研究结论

Date Results Publications
2021-03-13 13:15:00 Hypermethylated RASSF1 and SLC5A8 promoters alongside BRAF(V600E) mutation as biomarkers for papillary thyroid carcinoma. 32017063
2019-12-21 12:20:00 PDZRN3 may regulate SMCT1 function by interfering with the interaction between SMCT1 and PDZK1. 31098988
2019-08-17 12:55:00 SLC5A8 expression is repressed in human cervical cancer (CC) tumors and cell lines through epigenetic silencing. 30896789
2019-06-01 11:05:00 Results indicate that the SMCT1-PDZK1 interaction thus plays an important role in both lactate handling as well as urate reabsorption in the human kidney. 30604288
2019-01-26 12:41:00 Pendrin residues which are mutated in Pendred's syndrome are identical to those in the aligned position of sodium/iodide symporter (NIS) and apical iodide transporter (AIT). 29772533

名称对应

Type IDs
Synonymous AIT, SMCT, SMCT1
Gene
UniProtKB-ID: SC5A8_HUMAN
UniprotKB: Q8N695
UniParc: UPI000004DAF6
EMBL: CH471054, AY081220, BC110492, AF536217, AF536216, AC079953
Ensembl: ENSG00000262217, ENSG00000256870
KO: hsa:160728
Nucleutide sequences
EMBL-CDS: EAW97649.1, AAP46193.1, AAL88746.1, AAP46194.1, AAI10493.1
Ensembl_TRS: ENST00000572861, ENST00000536262
Protein sequencees
Ensembl_PRO: ENSP00000445340, ENSP00000461697
RefSeq: XP_016874399.1, NP_666018.3
Others
UniRef100: UniRef100_Q8N695
UniRef90: UniRef90_Q8N695
UniRef50: UniRef50_Q8N695
UniGene: Hs.444536
CCDS: CCDS9080.1

全选

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研究热度

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