MANF - Gene browser

MANF

mesencephalic astrocyte derived neurotrophic factor

HCNC Approved Symbol: MANF (HGNC:15461)
Genomic Coordinates: 3:51,385,291 - 51,389,397 (3p21.2)
Synonyms: ARP, ARMET
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

0Patient

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

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

No Results