ORF » Species Summary » Homo sapiens » KEGG » Porphyrin and chlorophyll metabolism

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Homo sapiens (human) Porphyrin and chlorophyll metabolism (provided by KEGG)

Browse by Letter Index, Genomic Locus

42 gene

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


Gene Symbol Full Name
UGT1A3 UDP glucuronosyltransferase family 1 member A3
BLVRA biliverdin reductase A
CPOX coproporphyrinogen oxidase
EARS2 glutamyl-tRNA synthetase 2, mitochondrial
UGT2B7 UDP glucuronosyltransferase family 2 member B7
BLVRB biliverdin reductase B
UGT1A4 UDP glucuronosyltransferase family 1 member A4
HMOX2 heme oxygenase 2
FXN frataxin
UGT1A6 UDP glucuronosyltransferase family 1 member A6
HMOX1 heme oxygenase 1
UGT2B17 UDP glucuronosyltransferase family 2 member B17
UGT1A5 UDP glucuronosyltransferase family 1 member A5
HEPH hephaestin
UGT2A3 UDP glucuronosyltransferase family 2 member A3
UGT2B28 UDP glucuronosyltransferase family 2 member B28
UGT2A2 UDP glucuronosyltransferase family 2 member A2
UGT2B15 UDP glucuronosyltransferase family 2 member B15
CP ceruloplasmin
UGT2A1 UDP glucuronosyltransferase family 2 member A1 complex locus
UGT1A8 UDP glucuronosyltransferase family 1 member A8
UGT1A10 UDP glucuronosyltransferase family 1 member A10
UROS uroporphyrinogen III synthase
UGT2B11 UDP glucuronosyltransferase family 2 member B11
ALAS1 5'-aminolevulinate synthase 1
ALAD aminolevulinate dehydratase
UGT1A9 UDP glucuronosyltransferase family 1 member A9
COX10 COX10, heme A:farnesyltransferase cytochrome c oxidase assembly factor
FECH ferrochelatase
UGT1A1 UDP glucuronosyltransferase family 1 member A1
HMBS hydroxymethylbilane synthase
HCCS holocytochrome c synthase
UGT2B4 UDP glucuronosyltransferase family 2 member B4
GUSB glucuronidase beta
UROD uroporphyrinogen decarboxylase
UGT2B10 UDP glucuronosyltransferase family 2 member B10
UGT1A7 UDP glucuronosyltransferase family 1 member A7
EPRS glutamyl-prolyl-tRNA synthetase
COX15 COX15, cytochrome c oxidase assembly homolog
ALAS2 5'-aminolevulinate synthase 2
MMAB methylmalonic aciduria (cobalamin deficiency) cblB type
PPOX protoporphyrinogen oxidase
ORF
overview_MB_2022