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USP17L7

ubiquitin specific peptidase 17 like family member 7

HCNC Approved Symbol
USP17L7 (HGNC:37180)
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.
However, there are 6 patients* with variant(s) predicted to be damaging.*3 of the patients have been diagnosed with a variant in another gene.

USP17L7 - Gene browser | 3billion