NR0B2 - Gene browser

NR0B2

nuclear receptor subfamily 0 group B member 2

HCNC Approved Symbol: NR0B2 (HGNC:7961)
Genomic Coordinates: 1:26,911,489 - 26,913,975 (1p36.11)
Synonyms: SHP
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

0Patient

There are no patients diagnosed with a variant in the NR0B2 gene.

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

No Results