Gene

krt96

ID

ZDB-GENE-030131-221

Name

keratin 96

Symbol

krt96 Nomenclature History

Previous Names

fb17f05
si:rp71-1n18.1
wu:fb17f05

Type

protein_coding_gene

Location

Chr: 22 Mapping Details/Browsers

Description

Predicted to enable structural molecule activity. Predicted to be located in intermediate filament. 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

Comparative Information

Expression

All Expression Data

No data available

Cross-Species Comparison

High Throughput Data

Expression Atlas

UO scRNA-seq (UCSC browser)

Single Cell Expression Atlas

Thisse Expression 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 krt96 Human Ortholog

No data available

Associated With krt96 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

Protein	Length	Intermediate filament, rod domain	Keratin, type I
UniProtKB:A0A8M1NXG3 InterPro	383

Transcripts

Genome Browsers

Type	Name	Annotation Method	Has Havana Data	Length (nt)	Analysis
mRNA	krt96-201 (1) Ensembl	Ensembl		1,438 nt	Select Tool ZFIN BLAST

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