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23150 FRMD4B

23150

FRMD4B

FERM domain containing 4B

protein-coding

Homo sapiens

基因描述

Type Description
Definition FERM domain containing 4B

研究结论

Date Results Publications
2010-12-04 11:06:00 association between the intronic rs6787362 FRMD4B SNP and ischemic cardiomyopathy in a European-derived population, but not FRMD4B variants as susceptibility factors in common heart failure 20718813
2010-09-15 22:06:00 Observational study of gene-disease association, gene-environment interaction, and pharmacogenomic / toxicogenomic. (HuGE Navigator) 20628086
2010-09-15 22:06:00 Observational study of gene-disease association. (HuGE Navigator) 20718813
2010-09-15 22:06:00 Observational study of gene-disease association. (HuGE Navigator) 19913121
2010-08-02 11:59:00 SNP is located in a 3' intronic region of the FRMD4B gene. FRMD4B as novel susceptibility loci for advanced heart failure. 20124441

名称对应

Type IDs
Synonymous 6030440G05Rik, GRSP1
Gene
UniProtKB-ID: FRM4B_HUMAN, E9PGA7_HUMAN, B3KNA2_HUMAN, Q6PEW6_HUMAN
UniprotKB: Q9Y2L6, E9PGA7, B3KNA2, Q6PEW6
UniParc: UPI00001CE057, UPI00006C066D, UPI00020530A9, UPI000015F6CA, UPI00001C1DF1
EMBL: BC057836, AB023230, DA339318, AC112212, AK024086, AC099328, AC112221, AC135851, BC028291
Ensembl: ENSG00000114541
KO: hsa:23150
Nucleutide sequences
EMBL-CDS: AAH28291.1, BAA76857.1, BAG51264.1, AAH57836.1
Ensembl_TRS: ENST00000398540, ENST00000478263
Protein sequencees
Ensembl_PRO: ENSP00000381549, ENSP00000418682
RefSeq: XP_016861479.1, XP_005264780.1, XP_016861485.1, XP_016861486.1, XP_016861484.1, XP_016861483.1, XP_016861482.1, XP_016861480.1, XP_016861481.1, XP_005264779.1, XP_016861478.1, NP_055938.2
Others
UniRef100: UniRef100_Q9Y2L6, UniRef100_Q6PEW6
UniRef90: UniRef90_Q6PEW6, UniRef90_Q920B0
UniRef50: UniRef50_A0A6A1Q9Z2, UniRef50_Q920B0
UniGene: Hs.709671
CCDS: CCDS46863.1

全选

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