ORF » Species Summary » Danio rerio » Reactome » Metabolism of water-soluble vitamins and cofactors

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.


Danio rerio (zebrafish) Metabolism of water-soluble vitamins and cofactors (provided by Reactome)

Browse by Letter Index, Genomic Locus

106 gene

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


Gene Symbol Full Name
mmaa methylmalonic aciduria (cobalamin deficiency) cblA type
mthfr methylenetetrahydrofolate reductase (NAD(P)H)
coasy CoA synthase
mibp muscle-specific beta 1 integrin binding protein
dhfr dihydrofolate reductase
cyb5r3 cytochrome b5 reductase 3
cyb5a cytochrome b5 type A (microsomal)
rfk riboflavin kinase
nmnat2 nicotinamide nucleotide adenylyltransferase 2
ptgs2b prostaglandin-endoperoxide synthase 2b
pank1b pantothenate kinase 1b
gphna gephyrin a
mut methylmalonyl CoA mutase
mthfd1b methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1b
btd biotinidase
LOC795699 solute carrier family 22 member 13-like
nmnat1 nicotinamide nucleotide adenylyltransferase 1
mthfd1l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1 like
flad1 flavin adenine dinucleotide synthetase 1
tpk1 thiamin pyrophosphokinase 1
aldh1l2 aldehyde dehydrogenase 1 family, member L2
acacb acetyl-CoA carboxylase beta
lmbrd1 LMBR1 domain containing 1
pcxa pyruvate carboxylase a
acp5a acid phosphatase 5a, tartrate resistant
mmachc methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
fasn fatty acid synthase
thtpa thiamine triphosphatase
ppcdc phosphopantothenoylcysteine decarboxylase
si:ch211-219a4.6 si:ch211-219a4.6
nt5e 5'-nucleotidase, ecto (CD73)
mocs3 molybdenum cofactor synthesis 3
LOC103911725 molybdopterin synthase catalytic subunit-like
slc2a3a solute carrier family 2 (facilitated glucose transporter), member 3a
nmrk2 nicotinamide riboside kinase 2
pdzd11 PDZ domain containing 11
mccc2 methylcrotonoyl-CoA carboxylase 2 (beta)
slc19a3a solute carrier family 19 (thiamine transporter), member 3a
slc22a13b solute carrier family 22 member 13b
zgc:64002 zgc:64002
shmt2 serine hydroxymethyltransferase 2 (mitochondrial)
slc5a6b solute carrier family 5 (sodium/multivitamin and iodide cotransporter), member 6
slc2a1a solute carrier family 2 (facilitated glucose transporter), member 1a
slc25a16 solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16
aasdhppt aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase
slc25a32a solute carrier family 25 (mitochondrial folate carrier), member 32a
mmadhc methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
mccc1 methylcrotonoyl-CoA carboxylase 1 (alpha)
naxe NAD(P)HX epimerase
slc2a1b solute carrier family 2 (facilitated glucose transporter), member 1b
nmnat1-rbp7a nmnat1-rbp7a readthrough
slc23a2 solute carrier family 23 (ascorbic acid transporter), member 2
slc5a8 solute carrier family 5 (sodium/monocarboxylate cotransporter), member 8
pcca propionyl CoA carboxylase, alpha polypeptide
pdxka pyridoxal (pyridoxine, vitamin B6) kinase a
enpp1 ectonucleotide pyrophosphatase/phosphodiesterase 1
mthfd2l methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2 like
shmt1 serine hydroxymethyltransferase 1 (soluble)
mtrr 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
slc19a2 solute carrier family 19 (thiamine transporter), member 2
gsto2 glutathione S-transferase omega 2
slc25a19 solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
slc52a3 solute carrier family 52 (riboflavin transporter), member 3
ptgs2a prostaglandin-endoperoxide synthase 2a
slc52a2 solute carrier family 52 (riboflavin transporter), member 2
mmab methylmalonic aciduria (cobalamin deficiency) cblB type
pank2 pantothenate kinase 2
mthfs 5,10-methenyltetrahydrofolate synthetase (5-formyltetrahydrofolate cyclo-ligase)
slc2a3b solute carrier family 2 (facilitated glucose transporter), member 3b
gsto1 glutathione S-transferase omega 1
slc19a3b solute carrier family 19 (thiamine transporter), member 3b
parp16 poly (ADP-ribose) polymerase family, member 16
mocs2 molybdenum cofactor synthesis 2
slc25a32b solute carrier family 25 (mitochondrial folate carrier), member 32b
si:dkey-145c18.3 si:dkey-145c18.3
si:dkey-145c18.2 si:dkey-145c18.2
abcd4 ATP-binding cassette, sub-family D (ALD), member 4
acaca acetyl-CoA carboxylase alpha
slc23a1 solute carrier family 23 (ascorbic acid transporter), member 1
nampta nicotinamide phosphoribosyltransferase a
ppcs phosphopantothenoylcysteine synthetase
naxd NAD(P)HX dehydratase
pank1a pantothenate kinase 1a
slc46a1 solute carrier family 46 (folate transporter), member 1
si:ch73-170l17.1 si:ch73-170l17.1
nmrk1 nicotinamide riboside kinase 1
naprt nicotinate phosphoribosyltransferase
mocs1 molybdenum cofactor synthesis 1
aldh1l1 aldehyde dehydrogenase 1 family, member L1
slc5a6a solute carrier family 5 (sodium/multivitamin and iodide cotransporter), member 6a
nfs1 NFS1 cysteine desulfurase
ela2l elastase 2 like
nudt12 nudix (nucleoside diphosphate linked moiety X)-type motif 12
prss1 protease, serine 1
fpgs folylpolyglutamate synthase
mthfd1a methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1a, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
pcxb pyruvate carboxylase b
pdxkb pyridoxal (pyridoxine, vitamin B6) kinase b
zgc:92335 zgc:92335
mthfd2 methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2, methenyltetrahydrofolate cyclohydrolase
< 1 2 > Total Pages 2
ORF
overview_MB_2022