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NCMAP

non-compact myelin associated protein

HCNC Approved Symbol
NCMAP (HGNC:29332)
Genomic Coordinates
: - (1p36.11)
Synonyms
FLJ42528, MP11, C1orf130
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
There are no patients* with variants predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

NCMAP - Gene browser | 3billion