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FAM187A

family with sequence similarity 187 member A

HCNC Approved Symbol
FAM187A (HGNC:35153)
Genomic Coordinates
: - (17q21.31)
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.
There are no patients* with variants predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

FAM187A - Gene browser | 3billion