abnormal circulating phospholipid level Gene Set
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
|