Type | Description |
---|---|
Definition | transmembrane 6 superfamily member 2 |
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 |
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
|
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Refseq |
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