Type | Description |
---|---|
Definition | FERM domain containing 4B |
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 |
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
|
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Refseq |
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