methylmalonic aciduria (cobalamin deficiency) cblB type homolog (human) [Source:MGI Symbol;Acc:MGI:1924947]
9130222L19Rik, ATP:Cob(I)alamin Adenosyltransferase
Chromosome 5: 114,569,095-114,582,121 reverse strand.
GRCm39:CM000998.3
This gene has 3 transcripts (splice variants), 199 orthologues and is associated with 6 phenotypes.