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FBXW10B

F-box and WD repeat domain containing 10B

HCNC Approved Symbol
FBXW10B (HGNC:14379)
Genomic Coordinates
17:15,565,482 - 15,619,704 (17p12)
Synonyms
HREP, SM25H2, FBXW10P1, CDRT1
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.

FBXW10B - Gene browser | 3billion