Gene
krt97
- ID
- ZDB-GENE-040718-78
- Name
- keratin 97
- Symbol
- krt97 Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 22 Mapping Details/Browsers
- Description
- Predicted to have structural molecule activity. Predicted to localize to intermediate filament. Human ortholog(s) of this gene implicated in several diseases, including autosomal recessive woolly hair 3; ectodermal dysplasia (multiple); epidermolysis bullosa simplex (multiple); epidermolytic hyperkeratosis; and palmoplantar keratosis (multiple). Is expressed in several structures, including EVL; fin; hatching gland; integument; and sensory system. 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
- 17 figures from 5 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- cb112 (10 images)
- cb481 (14 images)
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:Q6DHU3
|
438 |
Interactions and Pathways
No data available
Plasmids
No data available