abnormal apolipoprotein level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the amount of the a protein that is frequently a component of a lipoprotein complex (Mammalian Phenotype Ontology, MP_0010331)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010331
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4 gene mutations causing the abnormal apolipoprotein level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BPNT1 3'(2'), 5'-bisphosphate nucleotidase 1
OSBPL8 oxysterol binding protein-like 8
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
UTS2 urotensin 2