Reference Gene

Gene name Alias Species Exons Type Paralogs EC number OMIM
KRT86 keratin 86 HB6 , Hb1 , K86 , MNX , KRTHB1 , KRTHB6 Homo sapiens 11 protein-coding KRT8 , KRT6C , KRT6B , KRT6A , KRT80 , KRT74 , KRT71 , KRT72 , KRT73 , KRT77 , KRT78 , KRT4 , KRT79 , KRT76 , KRT3 , KRT2 , KRT1 , KRT75 , KRT5 , KRT85 , KRT81 , KRT83 , KRT84 , KRT82 , KRT7 601928

Summary

This gene encodes a type II keratin protein, which heterodimerizes with type I keratins to form hair and nails. This gene is present in a cluster of related genes and pseudogenes on chromosome 12. Mutations in this gene have been observed in patients with the hair disease monilethrix. [provided by RefSeq, Feb 2016]

GeneOntology

Gene Loss events - KRT86 (3 results)

GL_ID Species Order Gene Loss Mechanism Loss Type Lineage Specific Citation
GL_6XXDNF Tursiops truncatus Artiodactyla LOF (frameshift, premature stop, ss) Full No 10.1186/1471-2164-15-869
GL_FEFL8R Ursus maritimus Carnivora Other Full No 10.1186/s12983-017-0225-x
GL_GHRLZI Vicugna pacos Artiodactyla Gene deletion Full No 10.1186/s12983-017-0225-x