Type | Description |
---|---|
Definition | BMP/retinoic acid inducible neural specific 3 |
Date | Results | Publications |
---|---|---|
2017-12-23 10:12:00 | the association of serum OGN and FAM5C levels and muscle mass with bone mineral density (BMD), bone turnover markers, and the presence of vertebral fractures (VFs) in 156 postmenopausal women with type 2 diabetes mellitus, is reported. | 27836731 |
2017-10-28 11:55:00 | Data show that all the six inflammation-related CpG-SNPs genotypes including IL1B rs16944, IL1R2 rs2071008, PLA2G7 rs9395208, FAM5C rs12732361, CD40 rs1800686, and CD36 rs2065666 were associated with coronary heart disease (CHD), suggesting an important role of inflammation in the risk of CHD. | 27461004 |
2017-10-14 11:36:00 | FAM5C is a risk factor for cerebral infarction in type 2 diabetic patients. | 26717922 |
2017-06-03 11:58:00 | The results demonstrated that FAM5C is an N-glycosylated protein, and N-glycosylation by UGGT1 is necessary for the secretion of FAM5C. | 28351617 |
2016-10-08 10:07:00 | study provides evidence that the BRINP3 polymorphic variant rs1342913 and low level of BRINP3 expression are associated with peri-implantitis, independently from the presence of chronic periodontitis. | 25887438 |
Type | IDs |
---|---|
Synonymous | DBCCR1L, DBCCR1L1, FAM5C |
Gene |
UniProtKB-ID:
BRNP3_HUMAN
UniprotKB:
Q76B58
UniParc:
UPI00001C1D9A,
UPI0001914B48
EMBL:
U67037,
AL354771,
AL391645,
AL365402,
AK294365,
AK123024,
BC105054,
AB111893,
BC105052,
CH471067
Ensembl:
ENSG00000162670
KO:
hsa:339479
|
Nucleutide sequences |
EMBL-CDS:
EAW91222.1,
BAH11746.1,
BAG53853.1,
AAI05053.1,
AAD09521.1,
AAI05055.1,
BAD04066.1
Ensembl_TRS:
ENST00000367462
|
Protein sequencees |
Ensembl_PRO:
ENSP00000356432
RefSeq:
XP_011507777.1,
XP_016856615.1,
NP_001304117.1,
XP_016856622.1,
XP_016856621.1,
XP_016856619.1,
XP_016856618.1,
XP_016856614.1,
NP_950252.1,
XP_011507774.1,
XP_016856616.1,
XP_011507778.1,
XP_016856620.1,
XP_016856617.1
|
Others |
UniRef100:
UniRef100_Q76B58
UniRef90:
UniRef90_Q499E0
UniRef50:
UniRef50_Q499E0
UniGene:
Hs.65765
CCDS:
CCDS1373.1
|
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Refseq |
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