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MEP1B

meprin A subunit beta

HCNC Approved Symbol
MEP1B (HGNC:7020)
Genomic Coordinates
18:32,190,039 - 32,220,404 (18q12.1)
Synonyms
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 2 patients* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

MEP1B - Gene browser | 3billion