NR3C2
ENSG00000151623
Target class
Nuclear receptor
Chromosome
4
Approved drugs
11
Clinical candidates (approved and in development)
17
- Approved drugs
- 11
- ClinGen gene-disease validity
- Definitive
- Clinical candidates (approved and in development)
- 17
- Chemical probe available
- Yes
- Other names
- MR
- Target name
- NR3C2
- Gene name
- Nuclear receptor subfamily 3 group C member 2
- Gene symbol
- NR3C2
- Previous gene symbols
- MLR
- Protein name
- Mineralocorticoid receptor (MR) (Nuclear receptor subfamily 3 group C member 2)
- Gene biotype
- Protein coding
- Gene family
- Nuclear receptor subfamily 3 group C
- Target class
- Nuclear receptor
- Target type
- Human gene
- Tissues expressed in
- 51
- Protein localisation evidence grade
- Supported
- Highest tissue expression
- 19.31
- Tissue specificity (Gini)
- 0.292
- Tissue specificity (tau)
- 0.667
- KEGG gene identifiers
- hsa:4306
- Protein interaction confidence
- 0.827792
- Protein interaction partners
- 24
- R-HSA-3371497
- R-HSA-4090294
- End position
- 148445549
- Start position
- 148078762
- Chromosome
- 4
- Strand
- Reverse
- Cytoplasm. Nucleus. Endoplasmic reticulum membrane
- Peripheral membrane protein. Note=Cytoplasmic and nuclear in the absence of ligand
- nuclear after ligand-binding. When bound to HSD11B2, it is found associated with the endoplasmic reticulum membrane.
- Nucleoplasm
- Tissue specificity (tau)
- 0.666641
- Expression inequality (Gini)
- 0.292267
Expression in transcripts per million
- Thyroid
- 19.31
- Ovary
- 13.12
- Colon - Transverse
- 12.65
- Brain - Cerebellar Hemisphere
- 11.97
- Cervix - Ectocervix
- 11.78
Expression in transcripts per million
- Thyroid19.31
- Ovary13.12
- Colon - Transverse12.65
- Brain - Cerebellar Hemisphere11.97
- Cervix - Ectocervix11.78
- Artery - Tibial11.26
- Small Intestine - Terminal Ileum10.69
- Pituitary10.46
- Brain - Cerebellum10.14
- Nerve - Tibial10.02
- Bladder9.91
- Cervix - Endocervix9.58
- Colon - Sigmoid9.46
- Brain - Frontal Cortex (BA9)8.95
- Minor Salivary Gland8.57
- Breast - Mammary Tissue8.16
- Adipose - Subcutaneous8.07
- Testis8.04
- Brain - Cortex7.79
- Uterus7.65
- Kidney - Medulla7.37
- Lung7.32
- Fallopian Tube6.83
- Artery - Aorta6.64
- Vagina6.3
And 29 more, listed on the interactive page.
- GO:0007165
- GO:1901224
- GO:0005654
- GO:0005829
- GO:0043235
- GO:0003700
- GO:0003707
- GO:0005515
- GO:0017025
- GO:1990837
regulation of steroid hormone biosynthetic process
- cell-based: one of 12 assay component(s) measured or calculated from the CEETOX_H295R assay (11 hormones and 1 viability assay). It is designed to make measurements of hormone induction, a form of inducible reporter, as detected with absorbance signals by HPLC-MS-MS technology. The concentrations for these components have not been pre-filtered for the maximum tolerated concentration (MTC) based on the MTT assay (_noMTC).
- cell-based: one of 12 assay component(s) measured or calculated from the CEETOX_H295R assay (11 hormones and 1 viability assay). It is designed to make measurements of hormone induction, a form of inducible reporter, as detected with absorbance signals by HPLC-MS-MS technology. The concentrations for these components have not been pre-filtered for the maximum tolerated concentration (MTC) based on the MTT assay (_noMTC).
- cell-based: one of 12 assay component(s) measured or calculated from the CEETOX_H295R assay (11 hormones and 1 viability assay). It is designed to make measurements of hormone induction, a form of inducible reporter, as detected with absorbance signals by HPLC-MS-MS technology. The concentrations for these components have not been pre-filtered for the maximum tolerated concentration (MTC) based on the MTT assay (_noMTC).
- cell-based: one of 12 assay component(s) measured or calculated from the CEETOX_H295R assay (11 hormones and 1 viability assay). It is designed to make measurements of hormone induction, a form of inducible reporter, as detected with absorbance signals by HPLC-MS-MS technology. The concentrations for these components have not been pre-filtered for the maximum tolerated concentration (MTC) based on the MTT assay (_noMTC).
- cell-based: one of 12 assay component(s) measured or calculated from the CEETOX_H295R assay (11 hormones and 1 viability assay). It is designed to make measurements of hormone induction, a form of inducible reporter, as detected with absorbance signals by HPLC-MS-MS technology. The concentrations for these components have not been pre-filtered for the maximum tolerated concentration (MTC) based on the MTT assay (_noMTC).
- cell-based: one of 12 assay component(s) measured or calculated from the CEETOX_H295R assay (11 hormones and 1 viability assay). It is designed to make measurements of hormone induction, a form of inducible reporter, as detected with absorbance signals by HPLC-MS-MS technology. The concentrations for these components have not been pre-filtered for the maximum tolerated concentration (MTC) based on the MTT assay (_noMTC).
Biological samples
- H295R, cell line
Evidence sourceregulation of transcription factor activity
Studies
- cell-based
Biological samples
- HepG2, cell line
Evidence sourceregulation of steroid biosynthetic process
- cell-based: CEETOX_H295R_DOC, is one of 23 assay component(s) measured or calculated from the CEETOX_H295R assay. It is designed to make measurements of hormone induction, a form of inducible reporter, as detected with absorbance signals by HPLC-MS-MS technology.
- cell-based: CEETOX_H295R_CORTISOL, is one of 23 assay component(s) measured or calculated from the CEETOX_H295R assay. It is designed to make measurements of hormone induction, a form of inducible reporter, as detected with absorbance signals by HPLC-MS-MS technology.
- cell-based: CEETOX_H295R_CORTIC, is one of 23 assay component(s) measured or calculated from the CEETOX_H295R assay. It is designed to make measurements of hormone induction, a form of inducible reporter, as detected with absorbance signals by HPLC-MS-MS technology.
- cell-based: CEETOX_H295R_CORTIC, is one of 23 assay component(s) measured or calculated from the CEETOX_H295R assay. It is designed to make measurements of hormone induction, a form of inducible reporter, as detected with absorbance signals by HPLC-MS-MS technology.
- cell-based: CEETOX_H295R_11DCORT, is one of 23 assay component(s) measured or calculated from the CEETOX_H295R assay. It is designed to make measurements of hormone induction, a form of inducible reporter, as detected with absorbance signals by HPLC-MS-MS technology.
- cell-based: CEETOX_H295R_CORTISOL, is one of 23 assay component(s) measured or calculated from the CEETOX_H295R assay. It is designed to make measurements of hormone induction, a form of inducible reporter, as detected with absorbance signals by HPLC-MS-MS technology.
- cell-based: CEETOX_H295R_DOC, is one of 23 assay component(s) measured or calculated from the CEETOX_H295R assay. It is designed to make measurements of hormone induction, a form of inducible reporter, as detected with absorbance signals by HPLC-MS-MS technology.
- cell-based: CEETOX_H295R_11DCORT, is one of 23 assay component(s) measured or calculated from the CEETOX_H295R assay. It is designed to make measurements of hormone induction, a form of inducible reporter, as detected with absorbance signals by HPLC-MS-MS technology.
Biological samples
- H295R, cell line
Evidence source
Related records
Trials (883)
- "Dapagliflozin vs Dapagliflozin-Finerenone for Albuminuria in CKD With Type 2 Diabetes"
- "E4/DRSP Endocrine Function, Metabolic Control and Hemostasis Study"
- "Quick-starting" of a New Combined Hormonal Contraceptive Pills, 15 mg Estetrol/3 mg Drospirenone VS 20 mcg Ethinylestradiol/75 mcg Gestodene Focusing on Ovulation Inhibition
- 601 Versus Ranibizumab in Patients With Branch Retinal Vein Occlusion (BRVO)
- 601 Versus Ranibizumab in Patients With Central Retinal Vein Occlusion (CRVO)
- A Bioequivalence Study Between Fluticasone Propionate 250 mcg and Salmeterol Xinafoate 50 mcg Inhalation Powder/Respirent Pharmaceuticals vs. ADVAIR DISKUS® 250/50 Inhalation Powder/GSK in Healthy Volunteers
- A Bioequivalence Study Comparing A Fixed Dose Combination Formulation, Rin 150 And Individual Reference Drugs In Healthy Volunteers
- A Bioequivalence Study of Pegylated Interferon Alfa-2a (PEG-IFN Alfa-2a) Benzyl Alcohol (BA)-Free Formulation Versus PEG-IFN Alfa-2a (Pegasys) Following Subcutaneous Administration
- A Biomarker-targeted Clinical Trial to Optimize Treatment for Patients With Chronic Kidney Disease
- A Causal Role for Voltage-gated Cav1.2 Calcium Channels in Mediating 5G FR1 Effects on Sleep-associated Brain Health in Humans
- A Clinical Study Assessing the Effects of a Marketed Dentifrice on Tooth Sensitivity While Undergoing Tooth Bleaching
- A Clinical Study of IMC-001 for Injection in Improving Atherosclerotic Plaque Stability in Patients With Acute Coronary Syndrome.
- A Clinical Study to Assess an Experimental Dentifrice in an Experimental Model of Early Stage Caries
- A Clinical Trial to Evaluate the Efficacy, Tolerability, and Safety of a Fixed Dose Combination of Spironolactone, Pioglitazone & Metformin (SPIOMET) in Polycystic Ovary Syndrome (PCOS)
- A Comparative Study of New Formulation and Approved Formulation for Levothyroxine in Healthy Volunteers
- A Comparing Study Between SJ04 and Ovidrel® in Healthy Subjects
- A Comparison Of Outcomes In Patients In New York Heart Association (NYHA) Class II Heart Failure When Treated With Eplerenone Or Placebo In Addition To Standard Heart Failure Medicines
- A Cross-over Study Examining the Bioequivalence of 3 Test Formulations to a Reference Formulation of Alectinib (RO5424802) in Healthy Volunteers
- A Crossover Study to Evaluate the Relative Bioavailability of Two Formulations of Deuterated Remdesivir Hydrobromide for Oral Suspension in Healthy Chinese Adults
- A Drug-Drug Interaction Study Between HS-10374 Tablets and Drospirenone and Ethinyl Estradiol Tablets(Yasmin®)
Drugs (18)
- Balcinrenone Mineralocorticoid receptor modulator
- Canrenoate Mineralocorticoid receptor antagonist
- Canrenoate potassium Mineralocorticoid receptor antagonist
- Canrenone Mineralocorticoid receptor antagonist
- Desoxycorticosterone acetate Mineralocorticoid receptor agonist
- Desoxycorticosterone pivalate Mineralocorticoid receptor agonist
- Drospirenone Mineralocorticoid receptor antagonist
- Eplerenone Mineralocorticoid receptor antagonist
- Felodipine Mineralocorticoid receptor antagonist
- Finerenone Mineralocorticoid receptor antagonist
- Fludrocortisone acetate Mineralocorticoid receptor agonist
- LY2623091 Mineralocorticoid receptor antagonist
- MT-3995 Mineralocorticoid receptor antagonist
- Nimodipine Mineralocorticoid receptor antagonist
- PF-03882845 Mineralocorticoid receptor antagonist
- Spironolactone Mineralocorticoid receptor antagonist
- Vamorolone Mineralocorticoid receptor antagonist
- XL550 Mineralocorticoid receptor antagonist