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

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

Browse by Letter Index, Genomic Locus

137 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
apoa1a apolipoprotein A-Ia
cyb5a cytochrome b5 type A (microsomal)
rfk riboflavin kinase
nmnat2 nicotinamide nucleotide adenylyltransferase 2
ptgs2b prostaglandin-endoperoxide synthase 2b
pank1b pantothenate kinase 1b
apoa4b.2 apolipoprotein A-IV b, tandem duplicate 2
bco1l beta-carotene oxygenase 1, like
ubiad1 UbiA prenyltransferase domain containing 1
gphna gephyrin a
mut methylmalonyl CoA mutase
ttr transthyretin (prealbumin, amyloidosis type I)
mthfd1b methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1b
rbp4 retinol binding protein 4, plasma
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
si:ch211-119o8.7 si:ch211-119o8.7
apoa4b.1 apolipoprotein A-IV b, tandem duplicate 1
aldh1l2 aldehyde dehydrogenase 1 family, member L2
apoa4b.3 apolipoprotein A-IV b, tandem duplicate 3
acacb acetyl-CoA carboxylase beta
apoa1b apolipoprotein A-Ib
lmbrd1 LMBR1 domain containing 1
apoa4a apolipoprotein A-IV a
bco2a beta-carotene oxygenase 2a
pcxa pyruvate carboxylase a
acp5a acid phosphatase 5a, tartrate resistant
lrata lecithin retinol acyltransferase a
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
apobb.2 apolipoprotein Bb, tandem duplicate 2
slc25a16 solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16
bco2b beta-carotene oxygenase 2b
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
apobb.1 apolipoprotein Bb, tandem duplicate 1
rdh12 retinol dehydrogenase 12 (all-trans/9-cis/11-cis)
mccc1 methylcrotonoyl-CoA carboxylase 1 (alpha)
naxe NAD(P)HX epimerase
cyp2r1 cytochrome P450, family 2, subfamily R, polypeptide 1
akr1b1 aldo-keto reductase family 1, member B1 (aldose reductase)
slc2a1b solute carrier family 2 (facilitated glucose transporter), member 1b
nmnat1-rbp7a nmnat1-rbp7a readthrough
lratb.1 lecithin retinol acyltransferase b, tandem duplicate 1
slc23a2 solute carrier family 23 (ascorbic acid transporter), member 2
slc5a8 solute carrier family 5 (sodium/monocarboxylate cotransporter), member 8
gc group-specific component (vitamin D binding protein)
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)
cyp24a1 cytochrome P450, family 24, subfamily A, polypeptide 1
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
lgmn legumain
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
bco2l beta-carotene 15, 15-dioxygenase 2, like
si:dkey-145c18.3 si:dkey-145c18.3
si:dkey-145c18.2 si:dkey-145c18.2
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ORF
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