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C17orf49

chromosome 17 open reading frame 49

HCNC Approved Symbol
C17orf49 (HGNC:28737)
Genomic Coordinates
17:7,014,782 - 7,017,520 (17p13.1)
Synonyms
MGC49942, BAP18, HEPIS
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.

C17orf49 - Gene browser | 3billion