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Repository for lectin-assisted multimodality data
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MIRAGE
keratin 2
Summary
- Gene Symbol
-
- KRT2
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Coiled coil
- Cytoplasm
- Disease variant
- Ichthyosis
- Intermediate filament
- Keratin
- Methylation
- Phosphoprotein
- Proteomics identification
- Reference proteome
- Proteins
| UniProt | Protein Name |
|---|---|
| P35908 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| keratinocyte development | ||
| epidermis development | ||
| peptide cross-linking | ||
| keratinization | ||
| keratinization |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| structural constituent of cytoskeleton | ||
| protein binding | ||
| cytoskeletal protein binding | ||
| structural constituent of skin epidermis | ||
| structural constituent of skin epidermis |
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Keratin
- Functional Category
-
- E: Amino acid transport and metabolism
- O: Posttranslational modification, protein turnover, chaperones
- T: Signal transduction mechanisms
| Gene Ontology |
|---|
| intermediate filament organization |
| keratinization |
| structural constituent of skin epidermis |
| InterPro |
|---|
| Intermediate filament protein, conserved site |
| Intermediate filament, rod domain |
| Keratin type II head |
| Keratin, type II |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060877 | bullous congenital ichthyosiform erythroderma | |
| DOID:1697 | ichthyosis |
