ORF » Species Summary » Mus musculus » Reactome » Metabolism of water-soluble vitamins and cofactors
さらに検索するには こちらをクリック.
Browse by Letter Index, Genomic Locus
112 gene
The longest variant of each gene is displayed. Click the see gene variants link to see all gene variants.
Gene Symbol | Full Name |
---|---|
Slc2a1 | solute carrier family 2 (facilitated glucose transporter), member 1 |
Mmab | methylmalonic aciduria (cobalamin deficiency) cblB type homolog (human) |
Cd38 | CD38 antigen |
Acacb | acetyl-Coenzyme A carboxylase beta |
Parp10 | poly (ADP-ribose) polymerase family, member 10 |
Parp9 | poly (ADP-ribose) polymerase family, member 9 |
Flad1 | flavin adenine dinucleotide synthetase 1 |
Fpgs | folylpolyglutamyl synthetase |
Slc19a2 | solute carrier family 19 (thiamine transporter), member 2 |
Mthfd2l | methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2-like |
Ptgis | prostaglandin I2 (prostacyclin) synthase |
Shmt2 | serine hydroxymethyltransferase 2 (mitochondrial) |
Pank2 | pantothenate kinase 2 |
Acaca | acetyl-Coenzyme A carboxylase alpha |
Btd | biotinidase |
Cubn | cubilin (intrinsic factor-cobalamin receptor) |
Aldh1l1 | aldehyde dehydrogenase 1 family, member L1 |
Pnpo | pyridoxine 5'-phosphate oxidase |
Vnn1 | vanin 1 |
Ppcs | phosphopantothenoylcysteine synthetase |
Enpp1 | ectonucleotide pyrophosphatase/phosphodiesterase 1 |
Pcx | pyruvate carboxylase |
Slc19a1 | solute carrier family 19 (folate transporter), member 1 |
Aasdhppt | aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase |
Cyb5a | cytochrome b5 type A (microsomal) |
Nadk | NAD kinase |
Nfs1 | nitrogen fixation gene 1 (S. cerevisiae) |
Try10 | trypsin 10 |
Mccc2 | methylcrotonoyl-Coenzyme A carboxylase 2 (beta) |
Mocs3 | molybdenum cofactor synthesis 3 |
Pdxk | pyridoxal (pyridoxine, vitamin B6) kinase |
Mtrr | 5-methyltetrahydrofolate-homocysteine methyltransferase reductase |
Nampt | nicotinamide phosphoribosyltransferase |
Pdzd11 | PDZ domain containing 11 |
Nmrk1 | nicotinamide riboside kinase 1 |
Ptgs2 | prostaglandin-endoperoxide synthase 2 |
Nmnat1 | nicotinamide nucleotide adenylyltransferase 1 |
Parp16 | poly (ADP-ribose) polymerase family, member 16 |
Bst1 | bone marrow stromal cell antigen 1 |
Mmaa | methylmalonic aciduria (cobalamin deficiency) type A |
Thtpa | thiamine triphosphatase |
Rfk | riboflavin kinase |
Mut | methylmalonyl-Coenzyme A mutase |
Slc2a3 | solute carrier family 2 (facilitated glucose transporter), member 3 |
Gif | gastric intrinsic factor |
Slc23a1 | solute carrier family 23 (nucleobase transporters), member 1 |
Try5 | trypsin 5 |
Tpk1 | thiamine pyrophosphokinase |
Mthfr | methylenetetrahydrofolate reductase |
Fasn | fatty acid synthase |
Nnmt | nicotinamide N-methyltransferase |
Mccc1 | methylcrotonoyl-Coenzyme A carboxylase 1 (alpha) |
Lmbrd1 | LMBR1 domain containing 1 |
Mocs1 | molybdenum cofactor synthesis 1 |
Tcn2 | transcobalamin 2 |
Pank1 | pantothenate kinase 1 |
Shmt1 | serine hydroxymethyltransferase 1 (soluble) |
Slc52a2 | solute carrier protein 52, member 2 |
Prss2 | protease, serine 2 |
Mthfd2 | methylenetetrahydrofolate dehydrogenase (NAD+ dependent), methenyltetrahydrofolate cyclohydrolase |
Nmrk2 | nicotinamide riboside kinase 2 |
Naxe | NAD(P)HX epimerase |
Slc52a3 | solute carrier protein family 52, member 3 |
Coasy | Coenzyme A synthase |
Acp5 | acid phosphatase 5, tartrate resistant |
Gm10334 | predicted gene 10334 |
Mmadhc | methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria |
Hlcs | holocarboxylase synthetase (biotin- [propriony-Coenzyme A-carboxylase (ATP-hydrolysing)] ligase) |
Mthfs | 5, 10-methenyltetrahydrofolate synthetase |
Gsto2 | glutathione S-transferase omega 2 |
Aox1 | aldehyde oxidase 1 |
Mtr | 5-methyltetrahydrofolate-homocysteine methyltransferase |
Slc23a2 | solute carrier family 23 (nucleobase transporters), member 2 |
Prss1 | protease, serine 1 (trypsin 1) |
Slc5a6 | solute carrier family 5 (sodium-dependent vitamin transporter), member 6 |
Prss3 | protease, serine 3 |
Aldh1l2 | aldehyde dehydrogenase 1 family, member L2 |
Abcd4 | ATP-binding cassette, sub-family D (ALD), member 4 |
Nmnat2 | nicotinamide nucleotide adenylyltransferase 2 |
Pcca | propionyl-Coenzyme A carboxylase, alpha polypeptide |
Slc5a8 | solute carrier family 5 (iodide transporter), member 8 |
Naprt | nicotinate phosphoribosyltransferase |
Slc46a1 | solute carrier family 46, member 1 |
Ctrc | chymotrypsin C (caldecrin) |
Pccb | propionyl Coenzyme A carboxylase, beta polypeptide |
Folr2 | folate receptor 2 (fetal) |
Ppcdc | phosphopantothenoylcysteine decarboxylase |
Slc25a32 | solute carrier family 25, member 32 |
Amn | amnionless |
Mmachc | methylmalonic aciduria cblC type, with homocystinuria |
Mocs2 | molybdenum cofactor synthesis 2 |
Cyb5r3 | cytochrome b5 reductase 3 |
Try4 | trypsin 4 |
Nt5e | 5' nucleotidase, ecto |
Mthfd1 | methylenetetrahydrofolate dehydrogenase (NADP+ dependent), methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthase |
Nmnat3 | nicotinamide nucleotide adenylyltransferase 3 |
Qprt | quinolinate phosphoribosyltransferase |
Mthfsl | 5, 10-methenyltetrahydrofolate synthetase-like |
Naxd | NAD(P)HX dehydratase |
Gm5409 | predicted pseudogene 5409 |