MeSH term | MeSH ID | Detail |
---|---|---|
Sudden Infant Death | D013398 | 3 associated lipids |
Zellweger Syndrome | D015211 | 39 associated lipids |
Metabolic Syndrome | D024821 | 44 associated lipids |
Polycystic Kidney Diseases | D007690 | 12 associated lipids |
Lignoceric acid is a lipid of Fatty Acyls (FA) class. Lignoceric acid is associated with abnormalities such as Adrenoleukodystrophy and Peroxisomal Disorders. The involved functions are known as Anabolism, establishment and maintenance of localization, Saturated, Process and long-chain-fatty-acid-CoA ligase activity. Lignoceric acid often locates in Membrane, Microsomes, Plasma membrane, peroxisome and Mitochondria. The associated genes with Lignoceric acid are SLC27A1 gene, CD36 gene, F10 gene, INHA gene and ABCD1 gene. The related lipids are Sphingolipids, Fatty Acids, erucic acid, inositolphosphoceramides and Palmitates.
To understand associated biological information of Lignoceric acid, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.
Lignoceric acid is suspected in Peroxisomal Disorders, Adrenoleukodystrophy and other diseases in descending order of the highest number of associated sentences.
Disease | Cross reference | Weighted score | Related literature |
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We collected disease MeSH terms mapped to the references associated with Lignoceric acid
MeSH term | MeSH ID | Detail |
---|---|---|
Sudden Infant Death | D013398 | 3 associated lipids |
Zellweger Syndrome | D015211 | 39 associated lipids |
Metabolic Syndrome | D024821 | 44 associated lipids |
Polycystic Kidney Diseases | D007690 | 12 associated lipids |
There are no associated biomedical information in the current reference collection.
Associated locations are in red color. Not associated locations are in black.
Location | Cross reference | Weighted score | Related literatures |
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Function | Cross reference | Weighted score | Related literatures |
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Lipid concept | Cross reference | Weighted score | Related literatures |
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Gene | Cross reference | Weighted score | Related literatures |
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There are no associated biomedical information in the current reference collection.
Authors | Title | Published | Journal | PubMed Link |
---|---|---|---|---|
Jennemann R et al. | Novel glycoinositolphosphosphingolipids, basidiolipids, from Agaricus. | 1999 | Eur. J. Biochem. | pmid:9914511 |
Sandhir R et al. | Localization of nervonic acid beta-oxidation in human and rodent peroxisomes: impaired oxidation in Zellweger syndrome and X-linked adrenoleukodystrophy. | 1998 | J. Lipid Res. | pmid:9799802 |
Singh I et al. | Lovastatin and sodium phenylacetate normalize the levels of very long chain fatty acids in skin fibroblasts of X- adrenoleukodystrophy. | 1998 | FEBS Lett. | pmid:9600263 |
Suzuki Y et al. | Biochemical and immunocytochemical properties of peroxisomes and mitochondria in bovine chromaffin cells. | 1997 | Cell Struct. Funct. | pmid:9591053 |
Murad S et al. | Alpha-Hydroxylation of lignoceric and nervonic acids in the brain. Effects of altered thyroid function on postnatal development of the hydroxylase activity. | 1976 | J. Biol. Chem. | pmid:956184 |
Suzuki Y et al. | D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder. | 1997 | Am. J. Hum. Genet. | pmid:9345094 |
Hayashi H and Hara M | 1-Alkenyl group of ethanolamine plasmalogen derives mainly from de novo-synthesized fatty alcohol within peroxisomes, but not extraperoxisomal fatty alcohol or fatty acid. | 1997 | J. Biochem. | pmid:9192743 |
Bettger WJ and Blackadar CB | Dietary very long chain fatty acids directly influence the ratio of tetracosenoic (24:1) to tetracosanoic (24:0) acids of sphingomyelin in rat liver. | 1997 | Lipids | pmid:9075193 |
Inoue K et al. | Carrier identification of X-linked adrenoleukodystrophy by measurement of very long chain fatty acids and lignoceric acid oxidation. | 1996 | Clin. Genet. | pmid:9007322 |
Dawson G et al. | Mitochondrial abnormalities in CLN2 and CLN3 forms of Batten disease. | 1996 Oct-Dec | Mol. Chem. Neuropathol. | pmid:8971698 |