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DPM3

dolichyl-phosphate mannosyltransferase subunit 3, regulatory

HCNC Approved Symbol
DPM3 (HGNC:3007)
Genomic Coordinates
1:155,139,891 - 155,140,531 (1q22)
Synonyms
MGC34275, MGC125904, MGC125905
Disease Associations
This gene is associated with the following 2 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15
618992AR
Muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15
612937AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the DPM3 gene.

Frequently observed phenotypes

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

No Results