Entity Details

Primary name MLYCD
Entity type gene
Source Source Link

Details

PrimaryID23417
RefseqGeneNG_009079
SymbolMLYCD
Namemalonyl-CoA decarboxylase
Chromosome16
Location16q23.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-02-20
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsDCMC_HUMAN

GO terms

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GOName
GO:0002931 response to ischemia
GO:0005737 cytoplasm
GO:0005739 mitochondrion
GO:0005759 mitochondrial matrix
GO:0005777 peroxisome
GO:0005782 peroxisomal matrix
GO:0005829 cytosol
GO:0006085 acetyl-CoA biosynthetic process
GO:0006633 fatty acid biosynthetic process
GO:0006637 acyl-CoA metabolic process
GO:0008104 protein localization
GO:0010906 regulation of glucose metabolic process
GO:0019395 fatty acid oxidation
GO:0031998 regulation of fatty acid beta-oxidation
GO:0042802 identical protein binding
GO:0046321 positive regulation of fatty acid oxidation
GO:0050080 malonyl-CoA decarboxylase activity
GO:2001294 malonyl-CoA catabolic process

Diseases

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Disease IDSourceNameDescription
248360 OMIMMalonyl-CoA decarboxylase deficiency (MLYCD deficiency)Autosomal recessive disease characterized by abdominal pain, chronic constipation, episodic vomiting, metabolic acidosis and malonic aciduria. The disease is caused by variants affecting the gene represented in this entry.

Interactions

19 interactions