The KRT10 gene homepage

General information
Gene symbol KRT10
Gene name keratin 10
Chromosome 17
Chromosomal band q21.2
Imprinted -
Genomic reference NG_008405.1
Transcript reference NM_000421.3
Associated with diseases WD
Citation reference(s) -
Refseq URL Coding DNA reference sequence
Curators (0) -
Total number of public variants reported 0
Unique public DNA variants reported 0
Individuals with public variants 0
Hidden variants -
Notes This gene encodes a member of the type I (acidic) cytokeratin family, which belongs to the superfamily of intermediate filament (IF) proteins. Keratins are heteropolymeric structural proteins which form the intermediate filament. These filaments, along with actin microfilaments and microtubules, compose the cytoskeleton of epithelial cells. Mutations in this gene are associated with epidermolytic hyperkeratosis. This gene is located within a cluster of keratin family members on chromosome 17q21.
Date created October 28, 2013

Links to other resources
Homepage URL http://www.genomed.org/lovd3/genes/KRT10
HGNC 6413
Entrez Gene 3858
PubMed articles KRT10
OMIM - Gene 148080
OMIM - Diseases WD (wilson disease)
HGMD KRT10
GeneCards KRT10
GeneTests KRT10


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00000072 17 keratin 10 NM_000421.3 - -


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