Type | Description |
---|---|
Definition | neuromedin B receptor |
Date | Results | Publications |
---|---|---|
2020-05-09 13:14:00 | NMBR natural variants were enriched in patients with iron overload, and associated with facilitated iron absorption, possibly related to a defect of iron-induced hepcidin release. | 31724192 |
2017-02-18 11:07:00 | The rs2717 and rs6926279 within the NMBR gene were associated with schizophrenia liability. | 27092952 |
2014-10-11 11:12:00 | Hypoxia regulates the expression of the neuromedin B receptor through a mechanism dependent on hypoxia-inducible factor-1alpha. | 24349381 |
2010-12-05 22:08:00 | Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) | 21060863 |
2010-01-21 00:00:00 | NMB and its receptor are coexpressed by proliferating cells in which they act in an autocrine fashion with similar and modest potency in both normal and malignant colonic epithelial cells. | 15528253 |
Type | IDs |
---|---|
Synonymous | BB1, BB1R, NMB-R |
Gene |
UniProtKB-ID:
NMBR_HUMAN
UniprotKB:
P28336
UniParc:
UPI000013CFAB
EMBL:
AL589674,
GU727635,
CH471051,
M73482
Ensembl:
ENSG00000135577
KO:
hsa:4829
|
Nucleutide sequences |
EMBL-CDS:
EAW47886.1,
AAA59939.1,
ADU87637.1
Ensembl_TRS:
ENST00000258042
|
Protein sequencees |
Ensembl_PRO:
ENSP00000258042
RefSeq:
NP_001311236.1,
NP_002502.2,
NP_001311237.1
|
Others |
UniRef100:
UniRef100_P28336
UniRef90:
UniRef90_P28336
UniRef50:
UniRef50_P28336
UniGene:
Hs.654478
CCDS:
CCDS5196.1
|
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Refseq |
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