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FAM133B

family with sequence similarity 133 member B

HCNC Approved Symbol
FAM133B (HGNC:28629)
Genomic Coordinates
: - (7q21.2)
Synonyms
MGC40405
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.

FAM133B - Gene browser | 3billion