Gene

krt17

ID
ZDB-GENE-060503-86
Name
keratin 17
Symbol
krt17 Nomenclature History
Previous Names
  • si:dkeyp-113d7.7
Type
protein_coding_gene
Location
Chr: 19 Mapping Details/Browsers
Description
Predicted to have structural molecule activity. Involved in fin regeneration. Predicted to localize to intermediate filament. Is expressed in EVL. 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). Orthologous to several human genes including KRT17 (keratin 17).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
5 figures from 3 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 krt17 Human Ortholog
No data available
Associated With krt17 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
Homologous_superfamily IPR042180 Intermediate filament, rod domain, coil 1B
Domain Details Per Protein
Protein Length Intermediate filament, rod domain Intermediate filament, rod domain, coil 1B Keratin, type I
UniProtKB:Q1LXJ1 423
UniProtKB:I3ITC7 209
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
Name Type Antigen Genes Isotype Host Organism Assay Source Citations
Ab1-krt17 monoclonal IgG2b Mouse
  • WB
Thermo Scientific Pierce Protein Research Products
3
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations