|Homo sapiens Gene: KRT1|
|Last Modified||2014-10-13 [Report errors or provide feedback]|
|Gene Name||keratin 1|
|Synonyms||CK1; EHK; EHK1; EPPK; K1; KRT1A; NEPPK;|
|Useful resources||Stemformatics EHFPI ImmGen|
The protein encoded by this gene is a member of the keratin gene family. The type II cytokeratins consist of basic or neutral proteins which are arranged in pairs of heterotypic keratin chains coexpressed during differentiation of simple and stratified epithelial tissues. This type II cytokeratin is specifically expressed in the spinous and granular layers of the epidermis with family member KRT10 and mutations in these genes have been associated with bullous congenital ichthyosiform erythroderma. The type II cytokeratins are clustered in a region of chromosome 12q12-q13. [provided by RefSeq, Jul 2008]
|Genomic Location||Chromosome 12:52674736-52680407|
|Number of Interactions||
This gene and/or its encoded proteins are associated with 66 experimentally validated interaction(s) in this database.
They are also associated with 10 interaction(s) predicted by orthology.
Regulation of nuclear beta catenin signaling and target gene transcription
|UniProt Splice Variant|
|RNA Seq Atlas|