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4306 NR3C2

4306

NR3C2

nuclear receptor subfamily 3 group C member 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition nuclear receptor subfamily 3 group C member 2

研究结论

Date Results Publications
2021-02-02 13:23:00 Three Brothers With Autism Carry a Stop-Gain Mutation in the HPA-Axis Gene NR3C2. 32064789
2021-01-09 13:32:00 Sex-dependent association of mineralocorticoid receptor gene (NR3C2) DNA methylation and schizophrenia. 32712448
2021-01-02 12:53:00 Renin-aldosterone system evaluation over four decades in an extended family with autosomal dominant pseudohypoaldosteronism due to a deletion in the NR3C2 gene. 33017655
2020-12-05 12:59:00 Progesterone: An enigmatic ligand for the mineralocorticoid receptor. 32305433
2020-09-26 13:08:00 A novel NR3C2 polymorphism and the increased thyroid-stimulating hormone concentration are associated with venlafaxine treatment outcome in Chinese Han MDD patients. 31757642

名称对应

Type IDs
Synonymous MCR, MLR, MR, NR3C2VIT
Gene
UniProtKB-ID: MCR_HUMAN, B0ZBF6_HUMAN
UniprotKB: P08235, B0ZBF6
UniParc: UPI000006DED9, UPI0000457284, UPI000013DC6D, UPI0000367298
EMBL: AH006913, AJ315514, AC069272, FJ515829, M16801, AC104691, AJ315515, AC106899, AC093678, BC111758, AC093881, EU326312
Ensembl: ENSG00000151623
KO: hsa:4306
Nucleutide sequences
EMBL-CDS: ACS13717.1, CAC67406.1, ACS13716.1, CAC67405.1, ACA05924.1, AAI11759.1, AAA59571.1, AAC63513.1, ACA05925.1, ACS13715.1, ACA05923.1
Ensembl_TRS: ENST00000344721, ENST00000358102, ENST00000512865, ENST00000511528, ENST00000625323, ENST00000342437
Protein sequencees
Ensembl_PRO: ENSP00000341390, ENSP00000421481, ENSP00000343907, ENSP00000423510, ENSP00000350815, ENSP00000486719
RefSeq: XP_011530277.1, NP_001341748.1, XP_011530280.1, NP_001159576.1, NP_000892.2
Others
UniRef100: UniRef100_P08235
UniRef90: UniRef90_P08235
UniRef50: UniRef50_P08235
UniGene: Hs.163924
CCDS: CCDS54811.1, CCDS3772.1

全选

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