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Description	any anomaly in the concentration in the blood of the fat derivatives in which one fatty acid has been replaced by a phosphate group (Mammalian Phenotype Ontology, MP_0006084)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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Genes

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