Name: metabolism of cobalamin associated B
Synonyms: corrinoid adenosyltransferase, cilia and flagella associated protein 23, ATP:co(I)rrinoid adenosyltransferase MMAB, MGC20496, cob(II)alamin adenosyltransferase, methylmalonic aciduria (cobalamin deficiency) cblB type, ATP:cob(I)alamin adenosyltransferase, cobinamide/cobalamin adenosyltransferase, aquocob(I)alamin vitamin B12s adenosyltransferase, ATP:corrinoid adenosyltransferase, cob(I)alamin adenosyltransferase, cob, methylmalonic aciduria type B protein, methylmalonic aciduria (cobalamin deficiency) type b, corrinoid adenosyltransferase MMAB, cblB, cob(II)yrinic acid a,c-diamide adenosyltransferase, cob(I)yrinic acid a,c-diamide adenosyltransferase, mitochondrial, CFAP23, ATR
Source: HGNC:19331
Biotype: protein coding gene
Gene Synopsis: Mutations in the gene are the cause of vitamin B12-dependent methylmalonic aciduria linked to the cblB
Automated Gene Synopsis: Implicated in inherited metabolic disorder and methylmalonic acidemia cblB type.
Synonyms: cblB...methylmalonic aciduria (cobalamin deficiency) cblB type...cblB
Diseases: methylmalonic acidemia cblB type