Gene
krt17
- ID
- ZDB-GENE-060503-86
- Name
- keratin 17
- Symbol
- krt17 Nomenclature History
- Previous Names
-
- si:dkeyp-113d7.7
- Type
- protein_coding_gene
- Location
- Chr: 19 Mapping Details/Browsers
- Description
- Predicted to enable structural molecule activity. Acts upstream of or within fin regeneration. Predicted to be located in intermediate filament. Is expressed in EVL; eye; and trunk. Human ortholog(s) of this gene implicated in several diseases, including corneal dystrophy (multiple); ectodermal dysplasia (multiple); epidermolytic hyperkeratosis; focal nonepidermolytic palmoplantar keratoderma 1; and hereditary mucosal leukokeratosis. Orthologous to several human genes including KRT13 (keratin 13); KRT14 (keratin 14); and KRT15 (keratin 15).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 10 figures from 7 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Domain, Family, and Site Summary
Domain Details Per Protein
Protein | Length | Intermediate filament, rod domain | Keratin, type I |
---|---|---|---|
UniProtKB:Q1LXJ1
|
423 |
Interactions and Pathways
No data available
Name | Type | Antigen Genes | Isotype | Host Organism | Assay | Source | Citations |
---|---|---|---|---|---|---|---|
Ab1-krt17 | monoclonal | IgG2b | Mouse |
|
Thermo Scientific Pierce Protein Research Products
|
3 |
Plasmids
No data available