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FAM181B

family with sequence similarity 181 member B

HCNC Approved Symbol
FAM181B (HGNC:28512)
Genomic Coordinates
: - (11q14.1)
Synonyms
LOC220382, MGC33846
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.

FAM181B - Gene browser | 3billion