ORF » Species Summary » Homo sapiens » Reactome » Defects in cobalamin (B12) metabolism

ORF cDNAクローンを検索してください

検索サポート

以下のような検索ワードを入力できます：

  • 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)
  • 種名は、キーワードの後に ”キーワード[species:$species]” という形式で入力できます。ここで、$speciesは種の名称（ヒトやラットなど）、または分類群id　（9606など）を入力します。

さらに検索するには こちらをクリック.


Homo sapiens (human) Defects in cobalamin (B12) metabolism (provided by Reactome)

Browse by Letter Index, Genomic Locus

12 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
LOC107986404 uncharacterized LOC107986404
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
MMADHC methylmalonic aciduria and homocystinuria, cblD type
CD320 CD320 molecule
GIF gastric intrinsic factor
MMAA methylmalonic aciduria (cobalamin deficiency) cblA type
AMN amnion associated transmembrane protein
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
TCN2 transcobalamin 2
MUT methylmalonyl-CoA mutase
CUBN cubilin
ORF
overview_MB_2022