cob(I)alamin adenosyltransferase

Preferred Label : cob(I)alamin adenosyltransferase;

MeSH note : product of CblA gene; metabolic disorders due to deficient methylmalonyl-CoA mutase activity, a vitamin B12 (or cobalamin; Cbl)-dependent enzyme, resulting in some forms of methylmalonic aciduria; RefSeq NM_052845;

CISMeF synonym : methylmalonic aciduria (cobalamin deficiency) type B protein, human;

MeSH synonym : vitamin B12s adenosylating enzyme; deoxyadenosyltransferase; vitamin B12s adenosyltransferase;

Registry Number MeSH : EC 2.5.1.17;

Is substance : O;

UNII : EC 2.5.1.17;

Details

Origin ID

C019920;

UMLS CUI

C0056021;

False automatic mappings
- Methylmalonic acidemia [HPO term]
MeSH term(s) associated for indexing
- alkyl and aryl transferases [MeSH Descriptor]
Record concept(s)
- cob(I)alamin adenosyltransferase [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Enzyme [UMLS semantic type]
UMLS correspondences (same concept)
- Cob(I)alamin adenosyltransferase (substance) [SNOMED CT concept]
- cob(i)alamin adenosyltransferase [SNOMED Notion]

Keyword's position in hierarchy(ies) :

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