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Repository for lectin-assisted multimodality data
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MIRAGE
prominin 1
Summary
- Gene Symbol
-
- PROM1
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Acetylation
- Alternative splicing
- Cell membrane
- Cilium
- Coiled coil
- Cone-rod dystrophy
- Direct protein sequencing
- Disease variant
- Endoplasmic reticulum
- Glycoprotein
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Retinitis pigmentosa
- Signal
- Stargardt disease
- Transmembrane helix
- Proteins
| UniProt | Protein Name |
|---|---|
| O43490 |
|
| A0A0A0N0M1 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| retina layer formation | ||
| photoreceptor cell maintenance | ||
| photoreceptor cell maintenance | ||
| retina morphogenesis in camera-type eye | ||
| camera-type eye photoreceptor cell differentiation |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| photoreceptor outer segment | ||
| extracellular space | ||
| endoplasmic reticulum | ||
| endoplasmic reticulum-Golgi intermediate compartment | ||
| plasma membrane |
| GO Term | Evidence Code | PMID |
|---|---|---|
| protein binding | ||
| cholesterol binding | ||
| actinin binding | ||
| cadherin binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- prominin
- Functional Category
-
- P: Inorganic ion transport and metabolism
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| cholesterol binding |
| InterPro |
|---|
| Prominin |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0070517 | retinal macular dystrophy 2 | |
| DOID:0110376 | retinitis pigmentosa 41 | |
| DOID:0111019 | cone-rod dystrophy 12 |
