water-soluble vitamin metabolic process Gene Set

Dataset GO Biological Process Annotations
Category structural or functional annotations
Type biological process
Description The chemical reactions and pathways involving any of a diverse group of vitamins that are soluble in water. (Gene Ontology, GO_0006767)
External Link http://amigo.geneontology.org/amigo/term/GO:0006767
Similar Terms
Downloads & Tools

Genes

91 genes participating in the water-soluble vitamin metabolic process biological process from the curated GO Biological Process Annotations dataset.

Symbol Name
AASDHPPT aminoadipate-semialdehyde dehydrogenase-phosphopantetheinyl transferase
ABCC1 ATP-binding cassette, sub-family C (CFTR/MRP), member 1
ABCD4 ATP-binding cassette, sub-family D (ALD), member 4
ACACA acetyl-CoA carboxylase alpha
ACACB acetyl-CoA carboxylase beta
ACP5 acid phosphatase 5, tartrate resistant
ACPP acid phosphatase, prostate
AKR1A1 aldo-keto reductase family 1, member A1 (aldehyde reductase)
AMN amnion associated transmembrane protein
AOX1 aldehyde oxidase 1
BTD biotinidase
CD320 CD320 molecule
COASY CoA synthase
CTRB2 chymotrypsinogen B2
CUBN cubilin (intrinsic factor-cobalamin receptor)
CYB5A cytochrome b5 type A (microsomal)
CYB5R3 cytochrome b5 reductase 3
DHFR dihydrofolate reductase
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
FASN fatty acid synthase
FLAD1 flavin adenine dinucleotide synthetase 1
FOLR1 folate receptor 1 (adult)
FPGS folylpolyglutamate synthase
GCLC glutamate-cysteine ligase, catalytic subunit
GIF gastric intrinsic factor (vitamin B synthesis)
GPHN gephyrin
GSTO1 glutathione S-transferase omega 1
GSTO2 glutathione S-transferase omega 2
HLCS holocarboxylase synthetase (biotin-(proprionyl-CoA-carboxylase (ATP-hydrolysing)) ligase)
LMBRD1 LMBR1 domain containing 1
MCCC1 methylcrotonoyl-CoA carboxylase 1 (alpha)
MCCC2 methylcrotonoyl-CoA carboxylase 2 (beta)
MMAA methylmalonic aciduria (cobalamin deficiency) cblA type
MMAB methylmalonic aciduria (cobalamin deficiency) cblB type
MMACHC methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
MMADHC methylmalonic aciduria (cobalamin deficiency) cblD type, with homocystinuria
MOCOS molybdenum cofactor sulfurase
MOCS1 molybdenum cofactor synthesis 1
MOCS2 molybdenum cofactor synthesis 2
MOCS3 molybdenum cofactor synthesis 3
MTHFD1 methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 1, methenyltetrahydrofolate cyclohydrolase, formyltetrahydrofolate synthetase
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
MUT methylmalonyl CoA mutase
NADK NAD kinase
NADSYN1 NAD synthetase 1
NAMPT nicotinamide phosphoribosyltransferase
NAPRT nicotinate phosphoribosyltransferase
NFS1 NFS1 cysteine desulfurase
NMNAT1 nicotinamide nucleotide adenylyltransferase 1
NMNAT2 nicotinamide nucleotide adenylyltransferase 2
NMNAT3 nicotinamide nucleotide adenylyltransferase 3
PANK1 pantothenate kinase 1
PANK2 pantothenate kinase 2
PC pyruvate carboxylase
PCCA propionyl CoA carboxylase, alpha polypeptide
PCCB propionyl CoA carboxylase, beta polypeptide
PDXK pyridoxal (pyridoxine, vitamin B6) kinase
PDZD11 PDZ domain containing 11
PNPO pyridoxamine 5'-phosphate oxidase
PPCDC phosphopantothenoylcysteine decarboxylase
PPCS phosphopantothenoylcysteine synthetase
PRSS1 protease, serine, 1 (trypsin 1)
PRSS3 protease, serine, 3
PSAT1 phosphoserine aminotransferase 1
PTGIS prostaglandin I2 (prostacyclin) synthase
PTGS2 prostaglandin-endoperoxide synthase 2 (prostaglandin G/H synthase and cyclooxygenase)
QPRT quinolinate phosphoribosyltransferase
RFK riboflavin kinase
RGN regucalcin
SHMT1 serine hydroxymethyltransferase 1 (soluble)
SLC19A1 solute carrier family 19 (folate transporter), member 1
SLC19A2 solute carrier family 19 (thiamine transporter), member 2
SLC19A3 solute carrier family 19 (thiamine transporter), member 3
SLC23A1 solute carrier family 23 (ascorbic acid transporter), member 1
SLC23A2 solute carrier family 23 (ascorbic acid transporter), member 2
SLC25A16 solute carrier family 25 (mitochondrial carrier), member 16
SLC25A32 solute carrier family 25 (mitochondrial folate carrier), member 32
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
SLC2A3 solute carrier family 2 (facilitated glucose transporter), member 3
SLC46A1 solute carrier family 46 (folate transporter), member 1
SLC52A3 solute carrier family 52 (riboflavin transporter), member 3
SLC5A6 solute carrier family 5 (sodium/multivitamin and iodide cotransporter), member 6
TCN1 transcobalamin I (vitamin B12 binding protein, R binder family)
TCN2 transcobalamin II
THTPA thiamine triphosphatase
TKTL1 transketolase-like 1
TPK1 thiamin pyrophosphokinase 1
VNN1 vanin 1
VNN2 vanin 2