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53345 TM6SF2

53345

TM6SF2

transmembrane 6 superfamily member 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition transmembrane 6 superfamily member 2

研究结论

Date Results Publications
2021-04-03 13:36:00 Variants in PCSK7, PNPLA3 and TM6SF2 are risk factors for the development of cirrhosis in hereditary haemochromatosis. 33565643
2021-03-13 13:25:00 [Correlation between PNPLA3 rs738409 and TM6SF2 rs58542926 gene polymorphism and primary liver cancer in the Han Population of China's Northeast region]. 33685085
2021-02-20 13:30:00 Metabolic syndrome but not genetic polymorphisms known to induce NAFLD predicts increased total mortality in subjects with NAFLD (OPERA study). 31851849
2020-11-28 13:11:00 Independent and joint correlation of PNPLA3 I148M and TM6SF2 E167K variants with the risk of coronary heart disease in patients with non-alcoholic fatty liver disease. 32093693
2020-11-21 13:19:00 The TM6SF2 E167K genetic variant induces lipid biosynthesis and reduces apolipoprotein B secretion in human hepatic 3D spheroids. 31406127

名称对应

Type IDs
Gene
UniProtKB-ID: TM6S2_HUMAN, Q8N8A7_HUMAN
UniprotKB: Q9BZW4, Q8N8A7
UniParc: UPI0000366D60, UPI000006CD72, UPI0001E88EDE
EMBL: AC138430, BC120986, AF255923, AC003967, BC120987, AK097070, CH471106
Ensembl: ENSG00000213996
KO: hsa:53345
Nucleutide sequences
EMBL-CDS: AAG59700.1, AAI20987.1, AAI20988.1, EAW84807.1, BAC04941.1
Gene_ORFName: hCG_38579
Ensembl_TRS: ENST00000389363
Protein sequencees
Ensembl_PRO: ENSP00000374014
RefSeq: NP_001001524.2
Others
UniRef100: UniRef100_Q9BZW4, UniRef100_Q8N8A7
UniRef90: UniRef90_Q8N8A7, UniRef90_Q9BZW4
UniRef50: UniRef50_Q8N8A7, UniRef50_Q9BZW4
UniGene: Hs.531624
CCDS: CCDS42528.1

全选

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