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MMADHC


Official Full Name
metabolism of cobalamin associated D
Organism
Homo sapiens
Gene ID
27249
Background
This gene encodes a mitochondrial protein that is involved in an early step of vitamin B12 metabolism. Vitamin B12 (cobalamin) is essential for normal development and survival in humans. Mutations in this gene cause methylmalonic aciduria and homocystinuria type cblD (MMADHC), a disorder of cobalamin metabolism that is characterized by decreased levels of the coenzymes adenosylcobalamin and methylcobalamin. Pseudogenes have been identified on chromosomes 11 and X.[provided by RefSeq, Nov 2008]
Synonyms
HMAD; MACD; cblD; MAHCD; C2orf25; CL25022

Cat.No. Product Name Price
SHH342772 shRNA set against Human MMADHC (NM_015702.2) Inquiry
SHH342776 shRNA set against Mouse MMADHC (NM_133839.2) Inquiry
SHH342780 shRNA set against Rat MMADHC (NM_001004280.1) Inquiry
SHW000797 shRNA set against Chicken MMADHC (NM_001008477) Inquiry
SHW017518 shRNA set against Danio rerio MMADHC (NM_205594) Inquiry
Cat.No. Product Name Price
CDCB178993 Danio rerio MMADHC ORF Clone (NM_205594) Inquiry
CDFR001427 Rat Mmadhc cDNA Clone(NM_001004280.1) Inquiry
MiUTR1M-00323 MMADHC miRNA 3'UTR clone Inquiry
MiUTR1R-06407 MMADHC miRNA 3'UTR clone Inquiry
MiUTR3H-12213 MMADHC miRNA 3'UTR clone Inquiry
SKO0599 MMADHC Validated sgRNA vector Inquiry
CDCB162272 Chicken MMADHC ORF Clone (NM_001008477) Inquiry
CDCB194570 Rabbit MMADHC ORF clone (XM_002712155.2) Inquiry
CDCR368348 Rat Mmadhc ORF Clone(NM_001004280.1) Inquiry
CDCS419033 Human MMADHC ORF Clone (BC000932) Inquiry
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