tetrapyrrole metabolic process Gene Set

Dataset GO Biological Process Annotations
Category structural or functional annotations
Type biological process
Description The chemical reactions and pathways involving tetrapyrroles, natural pigments containing four pyrrole rings joined by one-carbon units linking position 2 of one pyrrole ring to position 5 of the next. (Gene Ontology, GO_0033013)
External Link http://amigo.geneontology.org/amigo/term/GO:0033013
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Genes

59 genes participating in the tetrapyrrole metabolic process biological process from the curated GO Biological Process Annotations dataset.

Symbol Name
ABCB6 ATP-binding cassette, sub-family B (MDR/TAP), member 6 (Langereis blood group)
ABCC1 ATP-binding cassette, sub-family C (CFTR/MRP), member 1
ABCD4 ATP-binding cassette, sub-family D (ALD), member 4
ALAD aminolevulinate dehydratase
ALAS1 5'-aminolevulinate synthase 1
ALAS2 5'-aminolevulinate synthase 2
AMBP alpha-1-microglobulin/bikunin precursor
AMN amnion associated transmembrane protein
ANK1 ankyrin 1, erythrocytic
ATPIF1 ATPase inhibitory factor 1
BDH2 3-hydroxybutyrate dehydrogenase, type 2
BLVRA biliverdin reductase A
BLVRB biliverdin reductase B
CD320 CD320 molecule
COX10 COX10 heme A:farnesyltransferase cytochrome c oxidase assembly factor
COX15 cytochrome c oxidase assembly homolog 15 (yeast)
CPOX coproporphyrinogen oxidase
CTRB2 chymotrypsinogen B2
CUBN cubilin (intrinsic factor-cobalamin receptor)
CYP1A1 cytochrome P450, family 1, subfamily A, polypeptide 1
CYP1A2 cytochrome P450, family 1, subfamily A, polypeptide 2
EIF2AK1 eukaryotic translation initiation factor 2-alpha kinase 1
FECH ferrochelatase
FXN frataxin
GIF gastric intrinsic factor (vitamin B synthesis)
HMBS hydroxymethylbilane synthase
HMOX1 heme oxygenase 1
HMOX2 heme oxygenase 2
HPX hemopexin
IBA57 IBA57, iron-sulfur cluster assembly homolog (S. cerevisiae)
IREB2 iron-responsive element binding protein 2
LMBRD1 LMBR1 domain containing 1
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
MTR 5-methyltetrahydrofolate-homocysteine methyltransferase
MTRR 5-methyltetrahydrofolate-homocysteine methyltransferase reductase
MUT methylmalonyl CoA mutase
NFE2L1 nuclear factor, erythroid 2-like 1
PPOX protoporphyrinogen oxidase
PRSS1 protease, serine, 1 (trypsin 1)
PRSS3 protease, serine, 3
RSAD1 radical S-adenosyl methionine domain containing 1
SLC11A2 solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2
SLC25A38 solute carrier family 25, member 38
SLC25A39 solute carrier family 25, member 39
SPTA1 spectrin, alpha, erythrocytic 1
SPTB spectrin, beta, erythrocytic
SUCLA2 succinate-CoA ligase, ADP-forming, beta subunit
TCN1 transcobalamin I (vitamin B12 binding protein, R binder family)
TCN2 transcobalamin II
TMEM14C transmembrane protein 14C
TNFRSF1A tumor necrosis factor receptor superfamily, member 1A
TSPO translocator protein (18kDa)
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1
UGT1A4 UDP glucuronosyltransferase 1 family, polypeptide A4
UROD uroporphyrinogen decarboxylase
UROS uroporphyrinogen III synthase