Entity Details

Primary name MMAA
Entity type gene
Source Source Link

Details

PrimaryID166785
RefseqGeneNG_007536
SymbolMMAA
Namemetabolism of cobalamin associated A
Chromosome4
Location4q31.21
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2002-01-26
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsMMAA_HUMAN

GO terms

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GOName
GO:0003924 GTPase activity
GO:0005525 GTP binding
GO:0005737 cytoplasm
GO:0005739 mitochondrion
GO:0005759 mitochondrial matrix
GO:0009235 cobalamin metabolic process
GO:0019626 short-chain fatty acid catabolic process
GO:0042802 identical protein binding
GO:0042803 protein homodimerization activity

Diseases

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Disease IDSourceNameDescription
251100 OMIMMethylmalonic aciduria type cblA (MMAA)A disorder of methylmalonate and cobalamin metabolism due to defective synthesis of adenosylcobalamin. The disease is caused by variants affecting the gene represented in this entry.

Interactions

5 interactions

InteractorPartnerSourcesPublicationsLink
MMAAMMUTBioGRID, HPRD, IntAct16641088 20876572 28497574 details
MMAAMMAABioGRID, IntAct20876572 details
MMAASIRT4IntAct25525879 details
MMAAH1-1BioGRID, IntAct30021884 details
MMAAINSBioGRID32457219 details