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MRAP

melanocortin 2 receptor accessory protein

HCNC Approved Symbol
MRAP (HGNC:1304)
Genomic Coordinates
21:32,291,813 - 32,314,784 (21q22.11)
Synonyms
B27, FALP, MRAP1, C21orf61
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 MRAP gene.

Frequently observed phenotypes

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

Adrenal insufficiency
 1 (100.0%)
MRAP - Gene browser | 3billion