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DPM1:DPM2 Y23C:DPM3 [endoplasmic reticulum membrane]
Stable Identifier
R-HSA-9631812
Type
Complex
Species
Homo sapiens
Compartment
endoplasmic reticulum membrane
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Diseases of glycosylation (Homo sapiens)
Diseases associated with glycosylation precursor biosynthesis (Homo sapiens)
Defective DPM2 causes DPM2-CDG (Homo sapiens)
Defective DPM2 does not transfer mannose to DOLP to form DOLPman (Homo sapiens)
DPM1:DPM2 Y23C:DPM3 [endoplasmic reticulum membrane] (Homo sapiens)
Participants
components
DPM1 [endoplasmic reticulum membrane]
(Homo sapiens)
DPM2 Y23C [endoplasmic reticulum membrane]
(Homo sapiens)
DPM3 [endoplasmic reticulum membrane]
(Homo sapiens)
Disease
Name
Identifier
Synonyms
congenital disorder of glycosylation type I
DOID:0050570
Cross References
ComplexPortal
CPX-6268
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