4306 |
NUCLEAR RECEPTOR SUBFAMILY 3 GROUP C MEMBER 2 |
NR3C2 |
MCR |
MLR |
MR |
NR3C2VIT |
600983 |
7979 |
ENSG00000151623 |
OTTHUMG00000161455 |
Mineralocorticoid receptor |
P08235 |
MCR_HUMAN |
MINERALOCORTICOID RECEPTOR (MR). [SOURCE:UNIPROT/SWISSPROT;ACC:P08235] |
PA242 |
T72168 |
Melanocortin receptor |
T45457 |
Target Class | Receptors |
Target Subclass | Nuclear receptor |
Interpro Acc | IPR000536 |
Interpro Name | Nuclear hormone receptor, ligand-binding, core |
Interpro Type | Domain |
Interpro Short Name | Nucl_hrmn_rcpt_lig-bd_core |
Uniprot Evidence | 1: Evidence at protein level |
Uniprot Status | Swiss-Prot |
Human Readable Name | DRUGGABLE GENOME |
Human Readable Name | NUCLEAR HORMONE RECEPTOR |
Initial Gene Query | NR3C2 |
Counted Citations from 1950-2000 | 2269 |
Target Main Class | Receptors |
Gene Biotype | PROTEIN_CODING |
NUCLEAR HORMONE RECEPTOR |
DRUGGABLE GENOME |
TRANSCRIPTION FACTOR |
antagonist (inhibitory) |
Novel drug target | Established target |
Trial Name | eplerenone tablets,Inspra |
Mechanism of Interaction | Mineralocorticoid receptor antagonist |
antagonist (inhibitory) |
Novel drug target | Established target |
Trial Name | ethinyl estradiol + drospirenone,Yaz |
Mechanism of Interaction | Mineralocorticoid receptor antagonist |
antagonist (inhibitory) |
Mechanism of Interaction | Mineralocorticoid receptor antagonist |
Direct Interaction | yes |
antagonist (inhibitory) |
Mechanism of Interaction | Mineralocorticoid receptor antagonist |
Direct Interaction | yes |
antagonist (inhibitory) |
Mechanism of Interaction | Mineralocorticoid receptor antagonist |
Direct Interaction | yes |
antagonist (inhibitory) |
Mechanism of Interaction | Mineralocorticoid receptor antagonist |
Direct Interaction | yes |
agonist (activating) |
Mechanism of Interaction | Mineralocorticoid receptor agonist |
Direct Interaction | yes |
antagonist (inhibitory) |
Mechanism of Interaction | Mineralocorticoid receptor antagonist |
Direct Interaction | yes |
agonist (activating) |
Direct Interaction | yes |
Mechanism of Interaction | Mineralocorticoid receptor agonist |
antagonist (inhibitory) |
Mechanism of Interaction | Mineralocorticoid receptor antagonist |
Direct Interaction | yes |
Trial Name | HTI-101 |
antagonist (inhibitory) |
Mechanism of Interaction | Mineralocorticoid receptor antagonist |
Direct Interaction | yes |
antagonist (inhibitory) |
Mechanism of Interaction | Mineralocorticoid receptor antagonist |
Direct Interaction | yes |
agonist (activating) |
antagonist (inhibitory) |
Trial Name | BHR-100 |
Novel drug target | Established target |
Trial Name | conjugated estrogens/medroxyprogesterone acetate,Prempro, Premphase |
NR3C2 | Ensembl Gene Name |
Gene Biotype | PROTEIN_CODING |
MINERALOCORTICOID RECEPTOR (MR). [SOURCE:UNIPROT/SWISSPROT;ACC:P08235] | Description |
NR3C2 | Display Id |
ENSG00000151623 | Ensembl Gene Id |
Human Readable Name | DRUGGABLE GENOME |
DRUGGABLE GENOME |
NR3C2 | Gene Symbol |
Target Class | Receptors |
Target Subclass | Nuclear receptor |
P08235 | Uniprot Accession |
4306 | Entrez Gene Id |
MCR_HUMAN | Uniprot Id |
Target Main Class | Receptors |
Target Subclass | Nuclear receptor |
4306 | Entrez Gene ID |
Initial Gene Query | NR3C2 |
Counted Citations from 1950-2000 | 2269 |
NUCLEAR HORMONE RECEPTOR |
MCR_HUMAN | Uniprot Id |
MINERALOCORTICOID RECEPTOR | Uniprot Protein Name |
ENSG00000151623 | Ensembl Gene Id |
Interpro Acc | IPR000536 |
Interpro Name | Nuclear hormone receptor, ligand-binding, core |
Interpro Type | Domain |
NUCLEAR HORMONE RECEPTOR, DRUGGABLE GENOME |
PA242 | PharmGKB ID |
ENSG00000151623 | Gene Symbol |
NR3C2 | Ensembl Id |
DRUGGABLE GENOME |
MLR | GENE_SYMBOL |
NR3C2 | GENE_SYMBOL |
Mineralocorticoid receptor | UNIPROT |
MCR | GO Gene Synonym |
MLR | GO Gene Synonym |
NUCLEAR HORMONE RECEPTOR |
4306 | Gene ID |
MCR | dGene Synonym |
MLR | dGene Synonym |
NUCLEAR HORMONE RECEPTOR |
MR | TTD Gene Abbreviation |
T72168 | TTD Target ID |
MCR | TTD Gene Abbreviation |
T45457 | TTD Target ID |
Mineralocorticoid receptor | Gene Name |
P08235 | UniProt ID |
TRANSCRIPTION FACTOR |