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FAM43B

family with sequence similarity 43 member B

HCNC Approved Symbol
FAM43B (HGNC:31791)
Genomic Coordinates
: - (1p36.12)
Synonyms
FLJ44952
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.

FAM43B - Gene browser | 3billion