NR3C1 - Gene browser | 3billion

NR3C1

NR3C1

nuclear receptor subfamily 3 group C member 1

HCNC Approved Symbol: NR3C1 (HGNC:7978)
Genomic Coordinates: 5:143,277,931 - 143,435,512 (5q31.3)
Synonyms: GR, GRL
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the NR3C1 gene.

Frequently observed phenotypes(Top 5 only)

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

01
Patient count

Cardiomyopathy, restrictive: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Cushing syndrome: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Hypertension: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30

NR3C1 - Gene browser | 3billion