Reference Gene

Gene name Alias Species Exons Type Paralogs EC number OMIM
KRT2 keratin 2 K2e , KRTE , CK-2e , KRT2A , KRT2E Homo sapiens 9 protein-coding KRT8 , KRT6C , KRT6B , KRT6A , KRT80 , KRT74 , KRT71 , KRT72 , KRT73 , KRT77 , KRT78 , KRT4 , KRT79 , KRT76 , KRT3 , KRT1 , KRT75 , KRT5 , KRT85 , KRT86 , KRT81 , KRT83 , KRT84 , KRT82 , KRT7 600194

Summary

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 expressed largely in the upper spinous layer of epidermal keratinocytes and mutations in this gene 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]

GeneOntology

Gene Loss events - KRT2 (12 results)

GL_ID Species Order Gene Loss Mechanism Loss Type Lineage Specific Citation
GL_TNUELL Hexaprotodon liberiensis Artiodactyla LOF (frameshift, premature stop, ss) Full Hippopotamidae 10.1016/j.cub.2021.02.057
GL_X1PSVT Physeter catodon Artiodactyla Gene deletion Full No 10.1016/j.cub.2021.02.057