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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 organic cyclic compound | ||
| angiogenesis | ||
| intrinsic apoptotic signaling pathway in response to oxidative stress | ||
| blood vessel morphogenesis | ||
| cellular response to cortisol stimulus |
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
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:3748 | esophagus squamous cell carcinoma | |
| DOID:3772 | intraventricular meningioma | |
| DOID:381 | arthropathy | |
| DOID:3829 | pituitary adenoma | |
| DOID:3852 | Peutz-Jeghers syndrome | |
| DOID:3861 | medullomyoblastoma | |
| DOID:3864 | adult medulloblastoma | |
| DOID:3868 | melanotic medulloblastoma | |
| DOID:3869 | childhood medulloblastoma | |
| DOID:3883 | Lynch syndrome |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0007906 | Ocular hypertension |
| HP:0007957 | Corneal opacity |
| HP:0007994 | Peripheral visual field loss |
| HP:0008007 | Primary congenital glaucoma |
| HP:0008041 | Late onset congenital glaucoma |
| HP:0011003 | High myopia |
| HP:0011483 | Anterior synechiae of the anterior chamber |
| HP:0011484 | Posterior synechiae of the anterior chamber |
| HP:0011490 | Abnormal Descemet membrane morphology |
| HP:0011493 | Central opacification of the cornea |
| 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 |
|---|---|---|---|
| 103178928 | CALMI16679 | ||
| 102362765 | LATCH13053 | ||
| 100150054 | ZFIN:ZDB-GENE-030902-1 | DANRE51342 | |
| 103036816 | ASTMX12103 | ||
| 100313516 | ICTPU26558 | ||
| 113579900 | ELEEL24477 | ||
| 106576803 | SALSA58343 | ||
| 106604807 | SALSA67237 | ||
| 115153034 | SALTR07184 | ||
| 115193979 | SALTR89651 |
