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FAM86B2

family with sequence similarity 86 member B2

HCNC Approved Symbol
FAM86B2 (HGNC:32222)
Genomic Coordinates
8:12,424,421 - 12,436,400 (8p23.1)
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.
There are no patients* with variants predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

FAM86B2 - Gene browser | 3billion