MMAA

Gene Symbol MMAA
Entrez Gene 166785
Alt Symbol cblA
Species Human
Gene Type protein-coding
Description methylmalonic aciduria (cobalamin deficiency) cblA type
Other Description methylmalonic aciduria type A protein, mitochondrial
Swissprots B3KX40 Q8IVH4 Q495G7
Accessions AAN77287 EAX05036 Q8IVH4 AK094722 AK126662 BAG54352 BC101178 AAI01179 BC101179 AAI01180 BC101180 AAI01181 BC101181 AAI01182 XM_011531684 XP_011529986 XM_011531685 XP_011529987 XM_011531686 XP_011529988 NM_172250 NP_758454
Function Probable GTPase. May function as chaperone. May be involved in the transport of cobalamin (Cbl) into mitochondria for the final steps of adenosylcobalamin (AdoCbl) synthesis.
Subcellular Location Mitochondrion {ECO:0000305}.
Tissue Specificity Widely expressed. Highest expression is observed in liver and skeletal muscle.

MMAA - MBS1266011 from MyBioSource

Prices $175.00
Sizes 10ug plasmid + 200ul glycerol stock
Species Human
Accession BC101179

Human MMAA Gene cDNA clone plasmid - HG15735-G from Sino Biological

Species Human

Human MMAA ORF Clone (BC101179) - CDCS417368 from Creative biogene

Species Human
Accession Q8IVH4
Search more