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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
cytochrome P450 family 11 subfamily B member 1
Summary
- Gene Symbol
-
- CYP11B1
- Aliases
-
- CPN1
- FHI
- P450C11
- steroid 11-beta-monooxygenase
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Alternative splicing
- Congenital adrenal hyperplasia
- Direct protein sequencing
- Disease variant
- Heme
- Mitochondrion inner membrane
- Monooxygenase
- Reference proteome
- Steroid biosynthesis
- Steroidogenesis
- Transit peptide
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| regulation of blood pressure | ||
| cortisol metabolic process | ||
| cholesterol metabolic process |
GO Hierarchy
biological process
metabolic process [inference]
biosynthetic process [inference]
primary metabolic process [inference]
small molecule metabolic process [inference]
organic substance metabolic process [inference]
cellular process [inference]
response to stimulus [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrial inner membrane | ||
| mitochondrion |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| steroid 11-beta-monooxygenase activity | ||
| corticosterone 18-monooxygenase activity | ||
| iron ion binding | ||
| heme binding |
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:5403 | microcystic adenoma | |
| DOID:576 | proteinuria | |
| DOID:5844 | myocardial infarction | |
| DOID:5854 | silent myocardial infarction | |
| DOID:6000 | congestive heart failure | |
| DOID:6204 | follicular adenoma | |
| DOID:656 | adrenal adenoma | |
| DOID:657 | adenoma | |
| DOID:660 | adrenal cortex cancer | |
| DOID:6713 | cerebrovascular disease |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000006 | Autosomal dominant inheritance |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000013 | Hypoplasia of the uterus |
| HP:0000040 | Long penis |
| HP:0000061 | Ambiguous genitalia, female |
| HP:0000062 | Ambiguous genitalia |
| HP:0000079 | Abnormality of the urinary system |
| HP:0000127 | Renal salt wasting |
| HP:0000147 | Polycystic ovaries |
| HP:0000360 | Tinnitus |
| Disease ID | Disease Name |
|---|---|
| ORPHA:90795 |
|
| OMIM:202010 |
|
| OMIM:103900 |
|
| ORPHA:403 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP002086
- Gene Name
- cytochrome P450, family 11, subfamily B, polypeptide 1
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 122210855 | PANLE18570 | ||
| 118883237 | BALMU01192 | ||
| 100654178 | LOXAF01708 | ||
| 100063612 | HORSE42961 | ||
| 100063645 | HORSE42957 | ||
| 110260194 | PIGXX22774 | ||
| 282422 | BOVIN05626 | ||
| 102188238 | CAPHI04983 | ||
| 106002066 | DIPOR23769 | ||
| 100771648 | CRIGR26193 |
