Search Your ORF cDNA Clones

Your can enter the following as search terms:

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)

Species can be input after the keyword, using format "keyword [species:$species]" where $species can be name of species (like human or rat) or taxon id (like 9606).

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

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
apoa4a	apolipoprotein A-IV a
tpk1	thiamin pyrophosphokinase 1
si:ch211-119o8.7	si:ch211-119o8.7
lrata	lecithin retinol acyltransferase a
mmachc	methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
fasn	fatty acid synthase
thtpa	thiamine triphosphatase
ppcdc	phosphopantothenoylcysteine decarboxylase
apoa1b	apolipoprotein A-Ib
lmbrd1	LMBR1 domain containing 1
si:ch211-219a4.6	si:ch211-219a4.6
nt5e	5'-nucleotidase, ecto (CD73)
mocs3	molybdenum cofactor synthesis 3
mthfd1l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1 like
apoa4b.3	apolipoprotein A-IV b, tandem duplicate 3
acacb	acetyl-CoA carboxylase beta
btd	biotinidase
LOC795699	solute carrier family 22 member 13-like
nmnat1	nicotinamide nucleotide adenylyltransferase 1
flad1	flavin adenine dinucleotide synthetase 1
apoa4b.1	apolipoprotein A-IV b, tandem duplicate 1
aldh1l2	aldehyde dehydrogenase 1 family, member L2
bco2a	beta-carotene oxygenase 2a
pcxa	pyruvate carboxylase a
acp5a	acid phosphatase 5a, tartrate resistant
LOC103911725	molybdopterin synthase catalytic subunit-like
nmrk2	nicotinamide riboside kinase 2
slc2a3a	solute carrier family 2 (facilitated glucose transporter), member 3a
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
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
gc	group-specific component (vitamin D binding protein)
enpp1	ectonucleotide pyrophosphatase/phosphodiesterase 1
cyp24a1	cytochrome P450, family 24, subfamily A, polypeptide 1
pcca	propionyl CoA carboxylase, alpha polypeptide
pdxka	pyridoxal (pyridoxine, vitamin B6) kinase a
mthfd2l	methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2 like
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
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
vkorc1	vitamin K epoxide reductase complex, subunit 1
slc23a1	solute carrier family 23 (ascorbic acid transporter), member 1