NR2F2 - Gene browser

NR2F2

nuclear receptor subfamily 2 group F member 2

HCNC Approved Symbol: NR2F2 (HGNC:7976)
Genomic Coordinates: 15:96,326,046 - 96,340,263 (15q26.2)
Synonyms: COUP-TFII, COUPTFB, SVP40, NF-E3, COUPTF2, ARP1, TFCOUP2
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

5Patients

In total, 5 patients were diagnosed with a variant in the NR2F2 gene.

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

05
Patient count

Atrial septal defect: 3 (60.0%)
Patient Count: 3 (60.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (60.0%)
Cryptorchidism: 3 (60.0%)
Patient Count: 3 (60.0%)
% of total patients presenting each phenotype is shown in parentheses.
3 (60.0%)
Ventricular septal defect: 2 (40.0%)
Patient Count: 2 (40.0%)
% of total patients presenting each phenotype is shown in parentheses.
2 (40.0%)
Congenital heart defect: 1 (20.0%)
Patient Count: 1 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (20.0%)
Conotruncal defect: 1 (20.0%)
Patient Count: 1 (20.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (20.0%)