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9159 PCSK7

9159

PCSK7

proprotein convertase subtilisin/kexin type 7

protein-coding

Homo sapiens

基因描述

Type Description
Definition proprotein convertase subtilisin/kexin type 7

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
2020-10-24 14:09:00 The motif EXEXXXL in the cytosolic tail of the secretory human proprotein convertase PC7 regulates its trafficking and cleavage activity. 31915245
2020-07-18 11:18:00 PCSK7 gene variation is associated with dyslipidemia and more severe liver disease in high risk individuals, likely by modulating PCSK7 expression/activity. 30918065
2017-04-08 11:58:00 Our present data suggest that PCSK7 as well as PCSK9 may be associated with lipids, especially triglyceride, and may serve as a candidate for a new drug target to treat lipid abnormality syndromes. 26763881
2017-03-25 10:57:00 PCSK7 rs236918 C allele is a risk factor for cirrhosis development in Italian patients with HFE-Hemochromatosis. 26868056

名称对应

Type IDs
Synonymous LPC, PC7, PC8, SPC7
Gene
UniProtKB-ID: PCSK7_HUMAN
UniprotKB: Q16549
UniParc: UPI0000070E4E
EMBL: BC010696, U40623, AB231710, AK312429, AK222907, BT006870, U33849, AF057710, CH471065, EF445005
Ensembl: ENSG00000160613
KO: hsa:9159
Nucleutide sequences
EMBL-CDS: ACA06036.1, ACA06037.1, AAD55137.1, AAH10696.1, BAD96627.1, BAG35338.1, EAW67305.1, AAP35516.1, AAB03087.1, AAC50417.1, BAE46876.1
Ensembl_TRS: ENST00000320934
Protein sequencees
Ensembl_PRO: ENSP00000325917
RefSeq: XP_006719003.1, XP_024304533.1, XP_024304532.1, NP_004707.2
Others
UniRef100: UniRef100_Q16549
UniRef90: UniRef90_Q16549
UniRef50: UniRef50_Q16549
UniGene: Hs.648612
CCDS: CCDS8382.1

全选

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