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Methylmalonic Aciduria and Homocystinuria Type D Protein, Mitochondrial

Go to external page http://purl.obolibrary.org/obo/NCIT_C74467

Methylmalonic aciduria and homocystinuria type D protein, mitochondrial (296 aa, ~33 kDa) is encoded by the human MMADHC gene. This protein plays a role in vitamin metabolism. [ ]

Term info

Label

Methylmalonic Aciduria and Homocystinuria Type D Protein, Mitochondrial

Synonyms
  • C2orf25 Protein
  • MMADHC
  • Methylmalonic Aciduria and Homocystinuria Type D Protein, Mitochondrial
  • Methylmalonic Aciduria, cblD Type, And Homocystinuria Protein
  • Uncharacterized Protein C2orf25, Mitochondrial
Legacy Concept Name

Uncharacterized_Protein_C2orf25_Mitochondrial

OMIM Number

611935

Preferred Name

Methylmalonic Aciduria and Homocystinuria Type D Protein, Mitochondrial

Semantic Type

Amino Acid, Peptide, or Protein

Swiss Prot

Q9H3L0

UMLS CUI

C2700105

code

C74467