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MIRAGE
cytochrome P450 family 19 subfamily A member 1
Summary
- Gene Symbol
-
- CYP19A1
- Aliases
-
- ARO
- ARO1
- CPV1
- CYAR
- P-450AROM
- aromatase
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Direct protein sequencing
- Disease variant
- Heme
- Lipid metabolism
- Membrane
- Microsome
- Monooxygenase
- Proteomics identification
- Pseudohermaphroditism
- Reference proteome
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| Q8IYG4 |
|
| P11511 |
|
| A8K6W3 |
|
| Q8TCA4 |
|
| Q05CU4 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| negative regulation of chronic inflammatory response | ||
| steroid biosynthetic process | ||
| estrogen biosynthetic process | ||
| androgen catabolic process | ||
| syncytium formation |
GO Hierarchy
biological process
metabolic process [inference]
biological regulation [inference]
regulation of biological process [inference]
regulation of immune system process [inference]
regulation of localization [inference]
regulation of locomotion [inference]
positive regulation of biological process [inference]
negative regulation of biological process [inference]
regulation of response to stimulus [inference]
regulation of cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum | ||
| endoplasmic reticulum | ||
| endoplasmic reticulum membrane | ||
| membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| iron ion binding | ||
| steroid hydroxylase activity | ||
| electron transfer activity | ||
| oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, reduced flavin or flavoprotein as one donor, and incorporation of one atom of oxygen | ||
| oxygen binding |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Rhea
- Enzyme
- PMID
- Enzyme
- PMID
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0090122 | aromatase excess syndrome | |
| DOID:10652 | Alzheimer's disease | |
| DOID:11476 | osteoporosis | |
| DOID:11612 | polycystic ovary syndrome | |
| DOID:12577 | urethral obstruction | |
| DOID:1380 | endometrial cancer | |
| DOID:13948 | bladder neck obstruction | |
| DOID:14654 | prostatitis | |
| DOID:1612 | breast cancer | |
| DOID:2394 | ovarian cancer |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000028 | Cryptorchidism |
| HP:0000061 | Ambiguous genitalia, female |
| HP:0000098 | Tall stature |
| HP:0000138 | Ovarian cyst |
| HP:0000771 | Gynecomastia |
| HP:0000786 | Primary amenorrhea |
| HP:0000815 | Hypergonadotropic hypogonadism |
| HP:0000855 | Insulin resistance |
| Disease ID | Disease Name |
|---|---|
| OMIM:139300 |
|
| ORPHA:91 |
|
| OMIM:613546 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP001780
- Gene Name
- cytochrome P450, family 19, subfamily A, polypeptide 1
