Lipid metabolism pathway

No Pathway Network information available for Lipid metabolism pathway

#	Name	Source	Genes
1	Lipid metabolism pathway	WikiPathways	ABHD5 ACACA ACLY ACSBG1 ACSS2 BCKDHA FASN HILPDA LIPE PDHA1 PLIN1 PNPLA2 PRKAA2 PRKAB1 PRKAR1B PRKAR2A PRKAR2B (see all 17) (see less)

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

#	Symbol	Description	Category	# Related Pathways
1	ACSS2	Acyl-CoA Synthetase Short Chain Family Member 2	Protein Coding	1
2	ACSBG1	Acyl-CoA Synthetase Bubblegum Family Member 1	Protein Coding	1
3	BCKDHA	Branched Chain Keto Acid Dehydrogenase E1 Subunit Alpha	Protein Coding	1
4	PNPLA2	Patatin Like Domain 2, Triacylglycerol Lipase	Protein Coding	1
5	PRKAR2B	Protein Kinase CAMP-Dependent Type II Regulatory Subunit Beta	Protein Coding	1
6	PRKAB1	Protein Kinase AMP-Activated Non-Catalytic Subunit Beta 1	Protein Coding	1
7	PRKAA2	Protein Kinase AMP-Activated Catalytic Subunit Alpha 2	Protein Coding	1
8	PLIN1	Perilipin 1	Protein Coding	1
9	PDHA1	Pyruvate Dehydrogenase E1 Subunit Alpha 1	Protein Coding	1
10	ABHD5	Abhydrolase Domain Containing 5, Lysophosphatidic Acid Acyltransferase	Protein Coding	1
11	ACLY	ATP Citrate Lyase	Protein Coding	1
12	LIPE	Lipase E, Hormone Sensitive Type	Protein Coding	1
13	ACACA	Acetyl-CoA Carboxylase Alpha	Protein Coding	1
14	HILPDA	Hypoxia Inducible Lipid Droplet Associated	Protein Coding	1
15	FASN	Fatty Acid Synthase	Protein Coding	1
16	PRKAR2A	Protein Kinase CAMP-Dependent Type II Regulatory Subunit Alpha	Protein Coding	1
17	PRKAR1B	Protein Kinase CAMP-Dependent Type I Regulatory Subunit Beta	Protein Coding	1

according to GeneCards Suite gene sharing

#	Disorder	Type	Genes	Score
1	Acetyl-coa carboxylase-alpha deficiency	Enrichment	ACACA	2.90
2	Prkar1b-related neurodegenerative dementia with intermediate filaments	Enrichment	PRKAR1B	2.90
3	Primary triglyceride deposit cardiomyovasculopathy	Enrichment	PNPLA2	2.90
4	Chanarin-dorfman syndrome	Enrichment	ABHD5	2.60
5	Neutral lipid storage disease with myopathy	Enrichment	PNPLA2	2.60
6	Marbach-schaaf neurodevelopmental syndrome	Enrichment	PRKAR1B	2.60
7	Ciliary dyskinesia, primary, 18	Enrichment	PRKAR1B	2.60
8	Maple syrup urine disease, type ia	Enrichment	BCKDHA	2.43
9	Lipodystrophy, familial partial, type 6	Enrichment	LIPE	2.43
10	Lipodystrophy, familial partial, type 4	Enrichment	PLIN1	2.43
11	Intermittent maple syrup urine disease	Enrichment	BCKDHA	2.43
12	Classic maple syrup urine disease	Enrichment	BCKDHA	2.43
13	Pyruvate dehydrogenase e1-alpha deficiency	Enrichment	PDHA1	2.30
14	Intermediate maple syrup urine disease	Enrichment	BCKDHA	2.30
15	Orofacial cleft 1	Enrichment	ACSS2	1.95
16	Sudden infant death syndrome	Enrichment	PDHA1	1.68
17	Primary ciliary dyskinesia	Enrichment	PRKAR1B	1.04

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 Lipid metabolism pathway