Gene
krt91
- ID
- ZDB-GENE-040801-181
- Name
- keratin 91
- Symbol
- krt91 Nomenclature History
- Previous Names
-
- fa97a07
- fb05e09
- krtt1c19a (1)
- wu:fa91b04
- wu:fa97a07
- wu:fb05e09
- zgc:92533
- Type
- protein_coding_gene
- Location
- Chr: 19 Mapping Details/Browsers
- Description
- Predicted to enable structural molecule activity. Predicted to be located in intermediate filament. Is expressed in EVL; epidermis; eye; and periderm. 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
- 17 figures from 6 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:92533 (14 images)
- IMAGE:6906914 (11 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:Q6DHB6
|
466 |
Interactions and Pathways
No data available
Plasmids
No data available