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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 |
|---|---|---|
| response to follicle-stimulating hormone | ||
| negative regulation of cell migration | ||
| positive regulation of smooth muscle cell migration | ||
| response to 3-methylcholanthrene | ||
| cellular response to progesterone 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:0110848 | xeroderma pigmentosum group F | |
| DOID:0110849 | xeroderma pigmentosum group G | |
| DOID:0110850 | xeroderma pigmentosum group B | |
| DOID:0111228 | Sveinsson chorioretinal atrophy | |
| DOID:0111441 | optic atrophy 1 | |
| DOID:0111529 | familial multiple nevi flammei | |
| DOID:10041 | dysplastic nevus syndrome | |
| DOID:11716 | prediabetes syndrome | |
| DOID:11771 | spontaneous ocular nystagmus | |
| DOID:10283 | prostate cancer |
- 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 |
|---|---|---|---|
| 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 |
