Glycerolipids and glycerophospholipids

No Pathway Network information available for Glycerolipids and glycerophospholipids

#	Name	Source	Genes
1	Glycerolipids and glycerophospholipids	WikiPathways	AGPAT4 CDIPT CDS1 CHKB CHPT1 CRLS1 DGAT1 DGAT2 DGKZ ETNK1 GPAM GPAT4 PCYT1A PCYT2 PEMT PISD PLA2G1B PLD1 PNPLA2 PTDSS1 PTDSS2 (see all 21) (see less)

Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways

#	Symbol	Description	Category	# Related Pathways
1	PTDSS2	Phosphatidylserine Synthase 2	Protein Coding	1
2	PCYT2	Phosphate Cytidylyltransferase 2, Ethanolamine	Protein Coding	1
3	AGPAT4	1-Acylglycerol-3-Phosphate O-Acyltransferase 4	Protein Coding	1
4	CRLS1	Cardiolipin Synthase 1	Protein Coding	1
5	PLA2G1B	Phospholipase A2 Group IB	Protein Coding	1
6	PISD	Phosphatidylserine Decarboxylase	Protein Coding	1
7	GPAT4	Glycerol-3-Phosphate Acyltransferase 4	Protein Coding	1
8	CDIPT	CDP-Diacylglycerol--Inositol 3-Phosphatidyltransferase	Protein Coding	1
9	PTDSS1	Phosphatidylserine Synthase 1	Protein Coding	1
10	DGAT1	Diacylglycerol O-Acyltransferase 1	Protein Coding	1
11	DGKZ	Diacylglycerol Kinase Zeta	Protein Coding	1
12	DGAT2	Diacylglycerol O-Acyltransferase 2	Protein Coding	1
13	GPAM	Glycerol-3-Phosphate Acyltransferase, Mitochondrial	Protein Coding	1
14	PNPLA2	Patatin Like Domain 2, Triacylglycerol Lipase	Protein Coding	1
15	CHPT1	Choline Phosphotransferase 1	Protein Coding	1
16	ETNK1	Ethanolamine Kinase 1	Protein Coding	1
17	PLD1	Phospholipase D1	Protein Coding	1
18	PCYT1A	Phosphate Cytidylyltransferase 1A, Choline	Protein Coding	1
19	CHKB	Choline Kinase Beta	Protein Coding	1
20	PEMT	Phosphatidylethanolamine N-Methyltransferase	Protein Coding	1
21	CDS1	CDP-Diacylglycerol Synthase 1	Protein Coding	1

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Lenz-majewski hyperostotic dwarfism	Enrichment	PTDSS1	2.81
2	Cardiac valvular dysplasia 1	Enrichment	PLD1	2.81
3	Proximal myopathy with focal depletion of mitochondria	Enrichment	CHKB	2.81
4	Combined oxidative phosphorylation deficiency 57	Enrichment	CRLS1	2.81
5	Autosomal dominant charcot-marie-tooth disease type 2 due to dgat2 mutation	Enrichment	DGAT2	2.81
6	Primary triglyceride deposit cardiomyovasculopathy	Enrichment	PNPLA2	2.81
7	Neutral lipid storage disease with myopathy	Enrichment	PNPLA2	2.51
8	Spondylometaphyseal dysplasia with cone-rod dystrophy	Enrichment	PCYT1A	2.51
9	Spastic paraplegia 82, autosomal recessive	Enrichment	PCYT2	2.51
10	Liberfarb syndrome	Enrichment	PISD	2.51
11	Lipodystrophy, congenital generalized, type 5	Enrichment	PCYT1A	2.51
12	Muscular dystrophy, congenital, megaconial type	Enrichment	CHKB	2.21
13	Diarrhea 7, protein-losing enteropathy type	Enrichment	DGAT1	2.21
14	Congenital diarrhea 7 with exudative enteropathy	Enrichment	DGAT1	2.11
15	Diarrhea	Enrichment	DGAT1	2.03
16	Muscular dystrophy	Enrichment	CHKB	1.44
17	Leber plus disease	Enrichment	PCYT1A	0.86

¹ WikiPathways

² PubChem

³ R&D Systems

⁴ Reactome

⁵ GeneGo (Thomson Reuters)

⁶ QIAGEN

⁷ PharmGKB

⁹ Sino Biological

¹⁰ Tocris

¹¹ MalaCards

Pathway Network for Glycerolipids and glycerophospholipids