ENSMUSG00000037022


Mus musculus

Features
Gene ID: ENSMUSG00000037022
  
Biological name :Mmaa
  
Synonyms : Methylmalonic aciduria type A homolog, mitochondrial / Mmaa / Q8C7H1
  
Possible biological names infered from orthology : methylmalonic aciduria (cobalamin deficiency) cblA type / Q8IVH4
  
Species: Mus musculus
  
Chr. number: 8
Strand: -1
Band: C1
Gene start: 79263598
Gene end: 79294937
  
Corresponding Affymetrix probe sets: 10579852 (MoGene1.0st)   1417857_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000048826
Ensembl peptide - ENSMUSP00000147987
NCBI entrez gene - 109136     See in Manteia.
MGI - MGI:1923805
RefSeq - XM_017312516
RefSeq - NM_133823
RefSeq - XM_017312513
RefSeq - XM_017312514
RefSeq - XM_017312515
RefSeq - XM_006530562
RefSeq - XM_006530563
RefSeq - XM_006530564
RefSeq - XM_006530565
RefSeq - XM_011248261
RefSeq - XM_011248262
RefSeq - XM_011248263
RefSeq - XM_011248264
RefSeq - XM_011248265
RefSeq - XM_011248266
RefSeq - XM_011248267
RefSeq - XM_011248268
RefSeq - XM_011248269
RefSeq - XM_011248270
RefSeq - XM_017312504
RefSeq - XM_017312505
RefSeq - XM_017312506
RefSeq - XM_017312507
RefSeq - XM_017312508
RefSeq - XM_017312509
RefSeq - XM_017312510
RefSeq - XM_017312511
RefSeq - XM_017312512
RefSeq Peptide - NP_598584
swissprot - Q8C7H1
swissprot - A0A1B0GSL6
Ensembl - ENSMUSG00000037022
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 mmaaENSDARG00000060383Danio rerio
 MMAAENSGALG00000009974Gallus gallus
 MMAAENSG00000151611Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR003593  AAA+ ATPase domain
 IPR005129  SIMIBI class G3E GTPase, ArgK/MeaB
 IPR027417  P-loop containing nucleoside triphosphate hydrolase


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0008150 biological_process ND
 biological_processGO:0009236 cobalamin biosynthetic process IEA
 cellular_componentGO:0005575 cellular_component ND
 cellular_componentGO:0005739 mitochondrion IEA
 molecular_functionGO:0000166 nucleotide binding IEA
 molecular_functionGO:0003924 GTPase activity IEA
 molecular_functionGO:0005525 GTP binding IEA
 molecular_functionGO:0016787 hydrolase activity IEA
 molecular_functionGO:0042802 identical protein binding IEA
 molecular_functionGO:0042803 protein homodimerization activity IEA


Pathways (from Reactome)
Pathway description
Cobalamin (Cbl, vitamin B12) transport and metabolism
Propionyl-CoA catabolism


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
No match
  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000037022 Mmaa / Q8C7H1 / Methylmalonic aciduria type A homolog, mitochondrial / Q8IVH4* / methylmalonic aciduria (cobalamin deficiency) cblA type*  / complex
 ENSMUSG00000023921 Mut / P16332 / Methylmalonyl-CoA mutase, mitochondrial / P22033* / methylmalonyl-CoA mutase*  / complex






 

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