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 have structural molecule activity. Predicted to localize to intermediate filament. Is expressed in EVL; epidermis; eye; and periderm. 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 KRT12 (keratin 12); KRT13 (keratin 13); and KRT14 (keratin 14).
Genome Resources
Note
None
Expression
All Expression Data
17 figures from 5 publications
Cross-Species Comparison
High Throughput Data
No data available
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 krt91 Human Ortholog
No data available
Associated With krt91 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:Q6DHB6 466
UniProtKB:F6PA25 58
Transcripts
Genome Browsers
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Ensembl Gene Tree
Citations