dpm1 Phenotypes

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Phenotypes

Gene Literature (1)

Nucleotides (162)

Interactants (73)

XB-GENEPAGE-976622

Gene Symbol: dpm1 Gene Name: dolichyl-phosphate mannosyltransferase polypeptide 1, catalytic subunit

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (48 sources): Abnormal macular morphology, Abnormality of the orbital region, Abnormality of vision, Ankle flexion contracture, Ataxia, Camptodactyly, Cerebral visual impairment, Depressed nasal bridge, Downslanted palpebral fissures, EEG abnormality, Elevated circulating creatine kinase concentration, Elevated circulating hepatic transaminase concentration, Failure to thrive, Flat occiput, Generalized hypotonia, Hemangioma, Hepatomegaly, High, narrow palate, Hypertelorism, Hypotonia, Knee flexion contracture, Lower limb hyperreflexia, Microcephaly, Micrognathia, Muscular dystrophy, Nail dysplasia, Nystagmus, Optic atrophy, Patent ductus arteriosus, Pontocerebellar atrophy, Prolonged partial thromboplastin time, Reduced antithrombin III activity, Reduced protein C activity, Reduced protein S activity, Respiratory distress, Retinopathy, Secondary microcephaly, Seizure, Severe global developmental delay, Short palm, Small hand, Smooth philtrum, Splenomegaly, Strabismus, Telangiectasia, Tremor, Type I transferrin isoform profile, Upper limb undergrowth [+]
Mouse (7 sources): abnormal chorion morphology, abnormal placenta morphology, abnormal trophoblast layer morphology, embryonic lethality during organogenesis, complete penetrance, increased trophoblast giant cell number, prenatal lethality prior to heart atrial septation, preweaning lethality, complete penetrance
View all ortholog results at Monarch