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P3H3

prolyl 3-hydroxylase 3

HCNC Approved Symbol
P3H3 (HGNC:19318)
Genomic Coordinates
12:6,828,407 - 6,839,847 (12p13.31)
Synonyms
GRCB, HSU47926, LEPREL2
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.

P3H3 - Gene browser | 3billion