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FAM78B

family with sequence similarity 78 member B

HCNC Approved Symbol
FAM78B (HGNC:13495)
Genomic Coordinates
: - (1q24.1)
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.
However, there is 1 patient* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

FAM78B - Gene browser | 3billion