abnormal circulating phospholipid level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the concentration in the blood of the fat derivatives in which one fatty acid has been replaced by a phosphate group (Mammalian Phenotype Ontology, MP_0006084)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0006084
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16 gene mutations causing the abnormal circulating phospholipid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
APOA1 apolipoprotein A-I
APOE apolipoprotein E
BHMT betaine--homocysteine S-methyltransferase
LCAT lecithin-cholesterol acyltransferase
LIPC lipase, hepatic
LIPG lipase, endothelial
LPL lipoprotein lipase
NPHP3 nephronophthisis 3 (adolescent)
NR1H4 nuclear receptor subfamily 1, group H, member 4
OSBPL8 oxysterol binding protein-like 8
PEX1 peroxisomal biogenesis factor 1
SAA1 serum amyloid A1
SCARB1 scavenger receptor class B, member 1
SPTLC2 serine palmitoyltransferase, long chain base subunit 2
TXNIP thioredoxin interacting protein