M1AP - Gene browser

M1AP

meiosis 1 associated protein

HCNC Approved Symbol: M1AP (HGNC:25183)
Genomic Coordinates: 2:74,557,883 - 74,648,330 (2p13.1)
Synonyms: D6Mm5e, SPATA37, C2orf65
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

0Patient

There are no patients diagnosed with a variant in the M1AP gene.

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

No Results