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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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MIRAGE
keratin 17
Summary
- Gene Symbol
-
- KRT17
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Coiled coil
- Cytoplasm
- Disease variant
- Ectodermal dysplasia
- Intermediate filament
- Isopeptide bond
- Keratin
- Palmoplantar keratoderma
- Phosphoprotein
- Reference proteome
- Ubl conjugation
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| positive regulation of translation | ||
| positive regulation of hair follicle development |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| cornified envelope | ||
| cytosol | ||
| cytoskeleton | ||
| intermediate filament | ||
| keratin filament |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| structural molecule activity | ||
| protein binding |
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 |
| InterPro |
|---|
| Intermediate filament, rod domain |
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050449 | pachyonychia congenita | |
| DOID:0111556 | steatocystoma multiplex | |
| DOID:2121 | ectodermal dysplasia |
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 7431 | WB:WBGene00002058 | ||
| 8687 | Xenbase:XB-GENE-19777908 | ||
| 9118 | WB:WBGene00002058 | ||
| 13346 | WB:WBGene00002058 | ||
| 14580 | WB:WBGene00002058 | ||
| 16667 | MOUSE03762 | ||
| 16669 | ZFIN:ZDB-GENE-991008-6 | ||
| 16691 | WB:WBGene00002058 | ||
| 22352 | WB:WBGene00002058 | ||
| 110310 | WB:WBGene00002058 |
