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FAM167B

family with sequence similarity 167 member B

HCNC Approved Symbol
FAM167B (HGNC:28133)
Genomic Coordinates
: - (1p35.2)
Synonyms
MGC10820, DIORA-2, C1orf90
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.

FAM167B - Gene browser | 3billion