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FAM47E

family with sequence similarity 47 member E

HCNC Approved Symbol
FAM47E (HGNC:34343)
Genomic Coordinates
: - (4q21.1)
Synonyms
FLJ42946, LOC100129583
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 are 2 patients* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

FAM47E - Gene browser | 3billion