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cytochrome P450 family 1 subfamily B member 1
Summary
- Gene Symbol
-
- CYP1B1
- Aliases
-
- CP1B
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Disease variant
- Fatty acid metabolism
- Glaucoma
- Heme
- Lipid metabolism
- Lyase
- Membrane
- Microsome
- Mitochondrion
- Monooxygenase
- Peters anomaly
- Reference proteome
- Steroid metabolism
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| cellular response to toxic substance | ||
| positive regulation of translation | ||
| retinal metabolic process | ||
| epoxygenase P450 pathway |
|
|
| cellular response to hydrogen peroxide |
GO Hierarchy
- response to nutrient
- response to arsenic-containing substance
biological process
metabolic process [inference]
cellular process [inference]
response to stimulus [inference]
response to endogenous stimulus [inference]
response to chemical [inference]
response to organic substance [inference]
cellular response to chemical stimulus [inference]
cellular response to stimulus [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of metabolic process [inference]
regulation of biosynthetic process [inference]
positive regulation of metabolic process [inference]
positive regulation of biosynthetic process [inference]
positive regulation of macromolecule metabolic process [inference]
positive regulation of cellular metabolic process [inference]
regulation of cellular metabolic process [inference]
regulation of nucleobase-containing compound metabolic process [inference]
positive regulation of cellular metabolic process [inference]
regulation of cellular biosynthetic process [inference]
regulation of nitrogen compound metabolic process [inference]
regulation of macromolecule metabolic process [inference]
regulation of primary metabolic process [inference]
regulation of locomotion [inference]
positive regulation of biological process [inference]
positive regulation of metabolic process [inference]
positive regulation of biosynthetic process [inference]
positive regulation of macromolecule metabolic process [inference]
positive regulation of cellular metabolic process [inference]
positive regulation of cellular process [inference]
regulation of cellular process [inference]
regulation of cellular metabolic process [inference]
regulation of nucleobase-containing compound metabolic process [inference]
positive regulation of cellular metabolic process [inference]
regulation of cellular biosynthetic process [inference]
positive regulation of cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| intracellular membrane-bounded organelle | ||
| endoplasmic reticulum membrane |
|
|
| mitochondrion |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| heme binding | ||
| estrogen 16-alpha-hydroxylase activity |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
KEGG BRITE Database
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:219 | colon cancer | |
| DOID:2224 | essential thrombocythemia | |
| DOID:2237 | hepatitis | |
| DOID:2348 | arteriosclerotic cardiovascular disease | |
| DOID:235 | colonic benign neoplasm | |
| DOID:2355 | anemia | |
| DOID:2361 | macrocytic anemia | |
| DOID:2377 | multiple sclerosis | |
| DOID:2394 | ovarian cancer | |
| DOID:2513 | basal cell carcinoma |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000486 | Strabismus |
| HP:0000501 | Glaucoma |
| HP:0000505 | Visual impairment |
| HP:0000523 | Subcapsular cataract |
| HP:0000525 | Abnormality iris morphology |
| HP:0000541 | Retinal detachment |
| HP:0000557 | Buphthalmos |
| HP:0000572 | Visual loss |
| HP:0000587 | Abnormal optic nerve morphology |
| Disease ID | Disease Name |
|---|---|
| OMIM:617315 |
|
| ORPHA:98976 |
|
| OMIM:600975 |
|
| ORPHA:98977 |
|
| ORPHA:708 |
|
| OMIM:231300 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 101612471 | JACJA11699 | ||
| 102417339 | MYOLU01592 | ||
| 117033397 | RHIFE24644 | ||
| 100230258 | TAEGU21715 | ||
| 103220462 | CHLSB04383 | ||
| 108520884 | RHIBE24276 | ||
| 104680972 | RHIRO39178 | ||
| 100583040 | NOMLE15392 | ||
| 114594484 | PODMU16720 | ||
| 107549156 | SINGR69202 |
