ENSG00000103150


Homo sapiens

Features
Gene ID: ENSG00000103150
  
Biological name :MLYCD
  
Synonyms : malonyl-CoA decarboxylase / MLYCD / O95822
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 16
Strand: 1
Band: q23.3
Gene start: 83899126
Gene end: 83927026
  
Corresponding Affymetrix probe sets: 218869_at (Human Genome U133 Plus 2.0 Array)   230530_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000262430
NCBI entrez gene - 23417     See in Manteia.
OMIM - 606761
RefSeq - NM_012213
RefSeq Peptide - NP_036345
swissprot - O95822
Ensembl - ENSG00000103150
  
Related genetic diseases (OMIM): 248360 - Malonyl-CoA decarboxylase deficiency, 248360
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 mlycdENSDARG00000104732Danio rerio
 ENSGALG00000005494Gallus gallus
 MlycdENSMUSG00000074064Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
AC009119.2ENSG0000026030024


Protein motifs (from Interpro)
Interpro ID Name
 IPR007956  Malonyl-CoA decarboxylase, C-terminal
 IPR035372  Malonyl-CoA decarboxylase, N-terminal


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0002931 response to ischemia ISS
 biological_processGO:0006085 acetyl-CoA biosynthetic process IEA
 biological_processGO:0006629 lipid metabolic process IEA
 biological_processGO:0006631 fatty acid metabolic process IEA
 biological_processGO:0006633 fatty acid biosynthetic process IDA
 biological_processGO:0006637 acyl-CoA metabolic process TAS
 biological_processGO:0010906 regulation of glucose metabolic process IMP
 biological_processGO:0046321 positive regulation of fatty acid oxidation IMP
 biological_processGO:2001294 malonyl-CoA catabolic process IDA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005739 mitochondrion IEA
 cellular_componentGO:0005759 mitochondrial matrix ISS
 cellular_componentGO:0005777 peroxisome IEA
 cellular_componentGO:0005782 peroxisomal matrix ISS
 molecular_functionGO:0005102 signaling receptor binding IPI
 molecular_functionGO:0016829 lyase activity IEA
 molecular_functionGO:0016831 carboxy-lyase activity IEA
 molecular_functionGO:0042802 identical protein binding IPI
 molecular_functionGO:0050080 malonyl-CoA decarboxylase activity TAS


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
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 HP:0001252 Muscular hypotonia "Muscular hypotonia is an abnormally low muscle tone (the amount of tension or resistance to movement in a muscle), often involving reduced muscle strength. Hypotonia is characterized by a diminished resistance to passive stretching." [HPO:curators]
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 HP:0001263 Developmental retardation "A delay in the achievement of motor or mental milestones manifested prior to age 18 and generally associated with lifelong mental and/or physical impairments." [HPO:curators]
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 HP:0001290 Generalized hypotonia "Generalized muscular hypotonia (abnormally low muscle tone)." [HPO:curators]
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 HP:0001302 Pachygyria "A congenital abnormality of the cerebral hemisphere chacterized by unusually thick gyrations (convolutions) of the cerebral cortex." [HPO:curators]
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 HP:0001639 Hypertrophic cardiomyopathy 
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 HP:0001942 Metabolic acidosis 
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 HP:0001943 Hypoglycemia "A lower than normal level of blood glucose." [HPO:curators]
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 HP:0001946 Ketosis 
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 HP:0002013 Vomiting 
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 HP:0002014 Diarrhea 
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 HP:0002019 Constipation 
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 HP:0002027 Abdominal pain 
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 HP:0003128 Lactic acidemia "An abnormal buildup of `lactic acid` (CHEBI:28358) in the body, leading to `acidification` (GO:0045851) of the blood." [HPO:probinson]
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 HP:0004322 Decreased body height "A height below that which is expected according to age and gender norms. Although there is no universally accepted definition of short stature, many refer to "short stature" as height more than 2 standard deviations below the mean for age and gender (or below the 3rd percentile for age and gender dependent norms)." [HPO:curators]
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 HP:0012450 Chronic constipation "Constipation for longer than three months with fewer than 3 bowel movements per week, straining, lumpy or hard stools, and a sensation of anorectal obstruction or incomplete defecation." [ORCID:0000-0001-5208-3432]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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