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CYP39A1

cytochrome P450 family 39 subfamily A member 1

HCNC Approved Symbol
CYP39A1 (HGNC:17449)
Genomic Coordinates
6:46,549,580 - 46,652,818 (6p12.3)
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 3 patients* with variant(s) predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

CYP39A1 - Gene browser | 3billion