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C17orf99

chromosome 17 open reading frame 99

HCNC Approved Symbol
C17orf99 (HGNC:34490)
Genomic Coordinates
: - (17q25.3)
Synonyms
GLPG464, UNQ464, IL-40
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 is 1 patient* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

C17orf99 - Gene browser | 3billion