ORF » Species Summary » Homo sapiens » Reactome » Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD

Search Your ORF cDNA Clones

Search Help

Your can enter the following as search terms:

  • Entrez Gene ID (e.g. 7157)
  • gene symbol (e.g. TP53)
  • gene name (e.g. tumor protein p53)
  • gene synonyms (e.g. FLJ92943)
  • Ensembl ID (e.g. ENSG0000141510)
  • Accession No. (e.g. NM_000546)
  • Species can be input after the keyword, using format "keyword [species:$species]" where $species can be name of species (like human or rat) or taxon id (like 9606).

Get more search, click here.


Homo sapiens (human) Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD (provided by Reactome)

Browse by Letter Index, Genomic Locus

2 gene

The longest variant of each gene is displayed. Click the see gene variants link to see all gene variants.


Gene Symbol Full Name
MMACHC methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
MMADHC methylmalonic aciduria and homocystinuria, cblD type
ORF

REQUEST A QUOTE

EMAIL

gene@genscript.com

PHONE

1-877-436-7274

ONLINE FORM

Online Quote Submission

ONLINE FORM

Online Quote Submission