Gene

krtt1c19e

ID
ZDB-GENE-050506-95
Name
keratin type 1 c19e
Symbol
krtt1c19e Nomenclature History
Previous Names
  • im:6905469 (1)
  • si:dkeyp-113d7.4
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 autosomal recessive woolly hair 3; corneal dystrophy (multiple); ectodermal dysplasia (multiple); epidermolysis bullosa simplex (multiple); and palmoplantar keratosis (multiple). Is expressed in corneal endothelial cell; epidermal basal stratum; and epidermis. Orthologous to several human genes including KRT12 (keratin 12); KRT13 (keratin 13); and KRT14 (keratin 14).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
6 figures from 2 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With krtt1c19e Human Ortholog
No data available
Associated With krtt1c19e Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR039008 Intermediate filament, rod domain
Family IPR002957 Keratin, type I
Domain Details Per Protein
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations