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USP17L29

ubiquitin specific peptidase 17 like family member 29

HCNC Approved Symbol
USP17L29 (HGNC:44457)
Genomic Coordinates
: - (4p16.1)
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.

USP17L29 - Gene browser | 3billion