Gene
krt96
- ID
- ZDB-GENE-030131-221
- Name
- keratin 96
- Symbol
- krt96 Nomenclature History
- Previous Names
-
- fb17f05
- si:rp71-1n18.1
- wu:fb17f05
- Type
- protein_coding_gene
- Location
- Chr: 22 Mapping Details/Browsers
- Description
- Predicted to be a structural constituent of skin epidermis. Predicted to be involved in morphogenesis of an epithelium. Predicted to be located in intermediate filament. Predicted to be active in keratin filament. Human ortholog(s) of this gene implicated in several diseases, including corneal dystrophy (multiple); ectodermal dysplasia (multiple); focal nonepidermolytic palmoplantar keratoderma 1; pachyonychia congenita; and steatocystoma multiplex. Orthologous to several human genes including KRT13 (keratin 13); KRT14 (keratin 14); and KRT15 (keratin 15).
- Genome Resources
- Note
-
- Comparative Information
-
- All Expression Data
- No data available
- 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 | Additional Resources | Length | Intermediate filament, rod domain | Keratin, type I |
|---|---|---|---|---|
| UniProtKB:A0A8M1NXG3 | InterPro | 383 |
Interactions and Pathways
No data available
Plasmids
No data available