Gene
krt1-19d
- ID
- ZDB-GENE-060316-1
- Name
- keratin, type 1, gene 19d
- Symbol
- krt1-19d Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 19 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 corneal dystrophy (multiple); ectodermal dysplasia (multiple); epidermolysis bullosa simplex (multiple); focal nonepidermolytic palmoplantar keratoderma 1; and hereditary mucosal leukokeratosis. Is expressed in epidermis. Orthologous to several human genes including KRT12 (keratin 12); KRT13 (keratin 13); and KRT14 (keratin 14).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Li et al., 2011
- 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:Q1LXK0
|
423 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
krt1-19d-201
(1)
|
Ensembl | 1,371 nt |
Interactions and Pathways
No data available
Plasmids
No data available