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USP17L8

ubiquitin specific peptidase 17 like family member 8

HCNC Approved Symbol
USP17L8 (HGNC:37181)
Genomic Coordinates
: - (8p23.1)
Synonyms
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.

USP17L8 - Gene browser | 3billion