Bos taurus Gene: DMGDH
Summary
InnateDB Gene IDBG-645212.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol DMGDH
Gene Name dimethylglycine dehydrogenase, mitochondrial
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000002110
Encoded Proteins
dimethylglycine dehydrogenase
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000132837:
This gene encodes an enzyme involved in the catabolism of choline, catalyzing the oxidative demethylation of dimethylglycine to form sarcosine. The enzyme is found as a monomer in the mitochondrial matrix, and uses flavin adenine dinucleotide and folate as cofactors. Mutation in this gene causes dimethylglycine dehydrogenase deficiency, characterized by a fishlike body odor, chronic muscle fatigue, and elevated levels of the muscle form of creatine kinase in serum. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 10:9994010-10066954
Strand Reverse strand
Band
Transcripts
ENSBTAT00000036611 ENSBTAP00000036467
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0004047 aminomethyltransferase activity
GO:0016491 oxidoreductase activity
GO:0044822 poly(A) RNA binding
GO:0047865 dimethylglycine dehydrogenase activity
Biological Process
GO:0006544 glycine metabolic process
GO:0006546 glycine catabolic process
GO:0032259 methylation
GO:0055114 oxidation-reduction process
Cellular Component
GO:0005737 cytoplasm
GO:0005739 mitochondrion
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
KEGG
Glycine, serine and threonine metabolism pathway
Glycine, serine and threonine metabolism pathway
INOH
Glycine Serine metabolism pathway
PID NCI
Cross-References
SwissProt
TrEMBL F1MDJ6
UniProt Splice Variant
Entrez Gene 504453
UniGene Bt.17379
RefSeq NM_001205545
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02027819
GenPept
RNA Seq Atlas 504453