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FAM221B

family with sequence similarity 221 member B

HCNC Approved Symbol
FAM221B (HGNC:30762)
Genomic Coordinates
: - (9p13.3)
Synonyms
C9orf128
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.* None of the patients have been diagnosed with a variant in another gene.

FAM221B - Gene browser | 3billion