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NR4A3

nuclear receptor subfamily 4 group A member 3

HCNC Approved Symbol
NR4A3 (HGNC:7982)
Genomic Coordinates
9:99,821,885 - 99,866,891 (9q31.1)
Synonyms
CSMF, CHN, NOR1, MINOR
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the NR4A3 gene.

Frequently observed phenotypes

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

No Results
NR4A3 - Gene browser | 3billion