Ethylmalonic acid

Ethylmalonic acid is a lipid of Fatty Acyls (FA) class. Ethylmalonic acid is associated with abnormalities such as Petechiae and Metabolic Diseases. The involved functions are known as Oxidation, Catabolic Process, Excretory function and Acidemia. Ethylmalonic acid often locates in Mitochondria. The associated genes with Ethylmalonic acid are N-caproylglycine and ETHE1 gene. The related lipids are Fatty Acids and sebacic acid.

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Introduction

To understand associated biological information of Ethylmalonic 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.

What diseases are associated with Ethylmalonic acid?

Ethylmalonic acid is suspected in Petechiae, Metabolic Diseases and other diseases in descending order of the highest number of associated sentences.

Related references are mostly published in these journals:

Disease Cross reference Weighted score Related literature
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Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with Ethylmalonic acid

MeSH term MeSH ID Detail
Brain Diseases D001927 27 associated lipids
Abnormalities, Multiple D000015 13 associated lipids
Intellectual Disability D008607 13 associated lipids
Metabolism, Inborn Errors D008661 46 associated lipids
Leukocytosis D007964 9 associated lipids
Lipid Metabolism, Inborn Errors D008052 26 associated lipids
Glomerulonephritis D005921 35 associated lipids
Brain Diseases, Metabolic, Inborn D020739 10 associated lipids
Vomiting D014839 21 associated lipids
Central Nervous System Diseases D002493 10 associated lipids
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PubChem Associated disorders and diseases

What pathways are associated with Ethylmalonic acid

Lipid pathways are not clear in current pathway databases. We organized associated pathways with Ethylmalonic acid through full-text articles, including metabolic pathways or pathways of biological mechanisms.

Related references are published most in these journals:

Pathway name Related literatures
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PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with Ethylmalonic acid?

Related references are published most in these journals:

Location Cross reference Weighted score Related literatures
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What functions are associated with Ethylmalonic acid?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with Ethylmalonic acid?

Related references are published most in these journals:

Lipid concept Cross reference Weighted score Related literatures
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What genes are associated with Ethylmalonic acid?

Related references are published most in these journals:


Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with Ethylmalonic acid?

There are no associated biomedical information in the current reference collection.

NCBI Entrez Crosslinks

All references with Ethylmalonic acid

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Authors Title Published Journal PubMed Link
Schuck PF et al. Promotion of lipid and protein oxidative damage in rat brain by ethylmalonic acid. 2010 Neurochem. Res. pmid:19757035
Srb V et al. Cytogenetic monitoring of a 24-hour effect of ethylmalonate platinum complex on human peripheral blood lymphocytes. 1986 Neoplasma pmid:3785467
Tiranti V et al. Loss of ETHE1, a mitochondrial dioxygenase, causes fatal sulfide toxicity in ethylmalonic encephalopathy. 2009 Nat. Med. pmid:19136963
Viscomi C et al. Combined treatment with oral metronidazole and N-acetylcysteine is effective in ethylmalonic encephalopathy. 2010 Nat. Med. pmid:20657580
Dusheiko G et al. Recurrent hypoglycemia associated with glutaric aciduria type II in an adult. 1979 N. Engl. J. Med. pmid:514320
Amaral AU et al. Ethylmalonic acid impairs brain mitochondrial succinate and malate transport. 2012 Mol. Genet. Metab. pmid:22133302
Westermann CM et al. Decreased oxidative phosphorylation and PGAM deficiency in horses suffering from atypical myopathy associated with acquired MADD. 2011 Mol. Genet. Metab. pmid:21843962
Di Rocco M et al. A case of ethylmalonic encephalopathy with atypical clinical and biochemical presentation. 2006 Mol. Genet. Metab. pmid:16828325
Gallant NM et al. Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in California. 2012 Mol. Genet. Metab. pmid:22424739
Nowaczyk MJ et al. Ethylmalonic and methylsuccinic aciduria in ethylmalonic encephalopathy arise from abnormal isoleucine metabolism. 1998 Metab. Clin. Exp. pmid:9667231