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399979 SNX19

399979

SNX19

sorting nexin 19

protein-coding

Homo sapiens

基因描述

Type Description
Definition sorting nexin 19

研究结论

Date Results Publications
2021-04-17 13:11:00 Schizophrenia risk variants influence multiple classes of transcripts of sorting nexin 19 (SNX19). 30635639
2010-04-07 21:40:00 Observational study of gene-disease association. (HuGE Navigator) 19752551
2009-12-02 21:41:00 Observational study of gene-disease association. (HuGE Navigator) 19730683
2009-03-25 21:36:00 Observational study of gene-disease association. (HuGE Navigator) 19023099
2008-12-03 21:30:00 Observational study of gene-disease association. (HuGE Navigator) 17975119

名称对应

Type IDs
Synonymous CHET8
Gene
UniProtKB-ID: SNX19_HUMAN, E9PJV7_HUMAN, B7ZAU9_HUMAN, E9PLV3_HUMAN
UniprotKB: Q92543, E9PJV7, B7ZAU9, E9PLV3
UniParc: UPI000013D6A5, UPI0001F77C33, UPI0001F77C32, UPI0001F77C31, UPI000191548A
EMBL: D87443, AP001093, BC031620, AF395843, AP000824, AK316414
Ensembl: ENSG00000120451
KO: hsa:399979
Nucleutide sequences
EMBL-CDS: AAK73124.1, BAA13384.2, AAH31620.1, BAH14785.1
Ensembl_TRS: ENST00000533214, ENST00000265909, ENST00000534726, ENST00000528555, ENST00000530356
Protein sequencees
Ensembl_PRO: ENSP00000435390, ENSP00000265909, ENSP00000433699, ENSP00000432307, ENSP00000435122
RefSeq: NP_001334854.1, NP_001288018.1, XP_011541127.1, NP_001334853.1, XP_011541123.1, NP_001334849.2, NP_001334852.2, NP_001334851.2, XP_011541122.1, NP_001334856.1, XP_011541128.1, NP_001334850.2, NP_001334848.2, NP_055573.3, XP_024304289.1, NP_001334847.2, XP_011541126.1, NP_001334855.1
Others
UniRef100: UniRef100_Q92543, UniRef100_B7ZAU9
UniRef90: UniRef90_Q92543, UniRef90_B7ZAU9
UniRef50: UniRef50_A0A384BVF4, UniRef50_Q92543
UniGene: Hs.444024
CCDS: CCDS86261.1, CCDS31721.1

全选

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