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54875 CNTLN

54875

CNTLN

centlein

protein-coding

Homo sapiens

基因描述

Type Description
Definition centlein

研究结论

Date Results Publications
2016-08-13 10:14:00 Taken together, we propose that centlein is involved in MT stability and neuritogenesis in vivo. 26915804
2014-12-06 11:18:00 Centlein complexes with C-Nap1 and Cep68 at the proximal ends of centrioles during interphase. 24554434
2013-03-23 11:09:00 identified a SNP (rs894379) in the intronic region of the centlein, centrosomal protein (CNTLN) gene on chromosome 9p22, whose minor allele G is associated with an increased left ventricular mass 22940680
2010-09-15 22:06:00 Observational study of gene-disease association. (HuGE Navigator) 19913121
2010-09-15 22:06:00 Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) 20628086

名称对应

Type IDs
Synonymous C9orf101, C9orf39, bA340N12.1
Gene
UniProtKB-ID: CNTLN_HUMAN, B1AMC8_HUMAN
UniprotKB: Q9NXG0, B1AMC8
UniParc: UPI000006CD2E, UPI0000458809, UPI000066DA4C, UPI000DEC0481
EMBL: AL133214, AK021596, AK098502, AK000283, AL354738, AL162725, AL354711, AK303973, AL590377
Ensembl: ENSG00000044459
KO: hsa:54875
Nucleutide sequences
EMBL-CDS: BAC05319.1, BAA91052.1, BAB13850.1, BAG64894.1
Ensembl_TRS: ENST00000380641, ENST00000380647
Protein sequencees
Ensembl_PRO: ENSP00000370021, ENSP00000370015
RefSeq: NP_001351958.1, NP_001273913.1, XP_016870335.1, NP_001107867.1, XP_016870333.1, XP_016870328.1, XP_011516243.1, XP_016870331.1, XP_006716856.1, XP_024303351.1, NP_001273914.1, XP_016870334.1, XP_016870336.1, NP_060208.2, XP_016870332.1, XP_016870329.1, XP_016870330.1
Others
UniRef100: UniRef100_Q9NXG0, UniRef100_B1AMC8
UniRef90: UniRef90_Q9NXG0, UniRef90_B1AMC8
UniRef50: UniRef50_Q9NXG0, UniRef50_B1AMC8
UniGene: Hs.435381
CCDS: CCDS47953.1, CCDS43789.1

全选

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