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4829 NMBR

4829

NMBR

neuromedin B receptor

protein-coding

Homo sapiens

基因描述

Type Description
Definition neuromedin B receptor

研究结论

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

名称对应

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

全选

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研究热度

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