CPOX
Summary: The protein encoded by this gene is the sixth enzyme of the heme biosynthetic pathway. The encoded enzyme is soluble and found in the intermembrane space of mitochondria. This enzyme catalyzes the stepwise oxidative decarboxylation of coproporphyrinogen III to protoporphyrinogen IX, a precursor of heme. Defects in this gene are a cause of hereditary coproporphyria (HCP).[provided by RefSeq, Oct 2009].
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Name | OMIM ID | Ensembl ID | HGNC ID | PHARMGKB ID | Map Location |
---|---|---|---|---|---|
OMIM IDMIM:612732 Ensembl IDEnsembl:ENSG00000080819 HGNC IDHGNC:HGNC:2321 PHARMGKB IDPA134979958 Map Location3q11.2 |
GO terms in CPOX
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Term Type | Evidence Type | GO Term ID | GO Des. |
---|---|---|---|
MF | IBA | GO:0004109 | coproporphyrinogen oxidase activity |
MF | TAS | GO:0004109 | coproporphyrinogen oxidase activity |
MF | IEA | GO:0005212 | structural constituent of eye lens |
MF | IDA | GO:0042803 | protein homodimerization activity |
BP | IEA | GO:0006782 | protoporphyrinogen IX biosynthetic process |
BP | TAS | GO:0006783 | heme biosynthetic process |
Gene expression in normal tissue: CPOX
Gene-model tissue-cancer distribution: Bubble Plot
Gene-drug pathway distribution
Pathways in CPOX
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Database | Pathway ID | Pathway Des. |
---|---|---|
smpdb | SMP00024 | Porphyrin Metabolism |
smpdb | SMP00342 | Hereditary Coproporphyria (HCP) |
smpdb | SMP00344 | Acute Intermittent Porphyria |
smpdb | SMP00345 | Congenital Erythropoietic Porphyria (CEP) or Gunther Disease |
smpdb | SMP00346 | Porphyria Variegata (PV) |
wikipathways | WP2004 | miR-targeted genes in lymphocytes - TarBase |
Gene-Drug: Aster Plot
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Drug ID | Drug Name | Model Num. |
---|---|---|
iGMDRD491 | TAE-684 | 1 |
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Gene in drug-gene network: Network Plot

Gene-drug targets distribution
Gene Structure: PDB
Models in CPOX
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Model | Level | Reference ID | Tissue | Cancer | Drug | Clinical Response | Source | |
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No matching records found |