Type | Description |
---|---|
Definition | nuclear receptor subfamily 3 group C member 2 |
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 |
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
|
{{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
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Refseq |
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