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UGT2B17

UDP glucuronosyltransferase family 2 member B17

HCNC Approved Symbol
UGT2B17 (HGNC:12547)
Genomic Coordinates
4:68,537,173 - 68,576,322 (4q13.2)
Synonyms
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
{Bone mineral density QTL 12, osteoporosis}
612560-

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the UGT2B17 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results