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80212 CCDC92

80212

CCDC92

coiled-coil domain containing 92

protein-coding

Homo sapiens

基因描述

Type Description
Definition coiled-coil domain containing 92

研究结论

Date Results Publications
2019-03-02 11:11:00 Novel genetic variants of CCDC92 were associated with both Diabetes and Coronary Artery Disease . 29731020
2018-08-18 10:50:00 The genotypic and allelic frequencies of the rs11057401 SNP of CCDC92 gene were significantly different between the patients with coronary heart disease and controls. 29439709
2017-10-28 11:42:00 Phenome-wide association scanning showed that CCDC92 likely affects coronary artery disease through insulin resistance pathways, whereas experimental analysis suggests that ARHGEF26 influences the transendothelial migration of leukocytes. 28714974
2017-09-09 11:49:00 Mutation in CCDC92 gene is associated with insulin-resistant cardiometabolic disease. 27841877
2010-01-20 21:35:00 Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) 19936222

名称对应

Type IDs
Gene
UniProtKB-ID: CCD92_HUMAN
UniprotKB: Q53HC0
UniParc: UPI0000141758, UPI000006FF96
EMBL: AK125866, AC079315, AC068790, AK054680, AK026124, AB015292, BC017186, AK222661
Ensembl: ENSG00000119242, ENSG00000275035
KO: hsa:80212
Nucleutide sequences
EMBL-CDS: BAB82436.1, BAG54259.1, BAB15366.1, BAG51412.1, BAD96381.1, AAH17186.1
Ensembl_TRS: ENST00000545891, ENST00000238156, ENST00000545135, ENST00000614047, ENST00000631749, ENST00000632401
Protein sequencees
Ensembl_PRO: ENSP00000479437, ENSP00000439526, ENSP00000487695, ENSP00000488830, ENSP00000440024, ENSP00000238156
RefSeq: XP_024304964.1, XP_024304960.1, XP_024304962.1, NP_001291887.1, NP_001291889.1, XP_024304963.1, NP_001291890.1, NP_079416.1, NP_001291888.1, XP_024304967.1, NP_001291886.1, XP_005253681.1, XP_024304961.1, XP_024304965.1
Others
UniRef100: UniRef100_Q53HC0
UniRef90: UniRef90_Q53HC0
UniRef50: UniRef50_Q53HC0
UniGene: Hs.713131
CCDS: CCDS76619.1, CCDS9256.1

全选

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