abnormal plasma membrane morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the semi-permeable membrane that encloses the cytoplasm of a cell (Mammalian Phenotype Ontology, MP_0003950)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003950
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14 gene mutations causing the abnormal plasma membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APOE apolipoprotein E
CAV1 caveolin 1, caveolae protein, 22kDa
CAV3 caveolin 3
CDK5RAP2 CDK5 regulatory subunit associated protein 2
DMD dystrophin
GAK cyclin G associated kinase
GLRX glutaredoxin (thioltransferase)
MPP4 membrane protein, palmitoylated 4 (MAGUK p55 subfamily member 4)
NPC1 Niemann-Pick disease, type C1
PIGA phosphatidylinositol glycan anchor biosynthesis, class A
PTRF polymerase I and transcript release factor
SDPR serum deprivation response
TJP2 tight junction protein 2
UGCG UDP-glucose ceramide glucosyltransferase