Reference Gene

Gene name Alias Species Exons Type Paralogs EC number OMIM
KRT9 keratin 9 K9 , CK-9 , EPPK , EPPK1 Homo sapiens 8 protein-coding BFSP2 , KRT18 , KRT24 , KRT23 , KRT33B , KRT34 , LOC100653049 , KRT33A , KRT31 , KRT40 , KRT38 , KRT37 , KRT39 , KRT35 , KRT32 , KRT36 , KRT19 , KRT27 , KRT28 , KRT25 , KRT26 , KRT10 , KRT12 , KRT17 , KRT20 , KRT16 , KRT14 , KRT15 , KRT13 607606

Summary

This gene encodes the type I keratin 9, an intermediate filament chain expressed only in the terminally differentiated epidermis of palms and soles. Mutations in this gene cause epidermolytic palmoplantar keratoderma. [provided by RefSeq, Jul 2008]

GeneOntology

Gene Loss events - KRT9 (11 results)

GL_ID Species Order Gene Loss Mechanism Loss Type Lineage Specific Citation
GL_S3SQTF Equus caballus Perissodactyla LOF (frameshift, premature stop, ss) Full No 10.1186/1471-2164-15-869