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MEP1A

meprin A subunit alpha

HCNC Approved Symbol
MEP1A (HGNC:7015)
Genomic Coordinates
6:46,793,389 - 46,845,984 (6p12.3)
Synonyms
PPHA
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
However, there are 3 patients* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

MEP1A - Gene browser | 3billion