ORF » Species Summary » Homo sapiens » Reactome » Cobalamin (Cbl, vitamin B12) transport and metabolism

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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。

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Homo sapiens (human) Cobalamin (Cbl, vitamin B12) transport and metabolism (provided by Reactome)

Browse by Letter Index, Genomic Locus

22 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
PRSS3 serine protease 3
ABCD4 ATP binding cassette subfamily D member 4
CD320 CD320 molecule
GIF gastric intrinsic factor
PRSS1 serine protease 1
TCN1 transcobalamin 1
MMAA methylmalonic aciduria (cobalamin deficiency) cblA type
AMN amnion associated transmembrane protein
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
LMBRD1 LMBR1 domain containing 1
ABCC1 ATP binding cassette subfamily C member 1
CTRC chymotrypsin C
TCN2 transcobalamin 2
CTRB1 chymotrypsinogen B1
CTRB2 chymotrypsinogen B2
MUT methylmalonyl-CoA mutase
MMAB methylmalonic aciduria (cobalamin deficiency) cblB type
CUBN cubilin
ORF
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