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Gene information for KRT86 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID3892
Official gene symbolKRT86
Full namekeratin 86
Aliases,FLJ25176,HB6,Hb1,KRTHB1,KRTHB6,MNX,hHb6,
Gene summaryThe protein encoded by this gene is a member of the keratin gene family. As a type II hair keratin, it is a basic protein which heterodimerizes with type I keratins to form hair and nails. The type II hair keratins are clustered in a region of chromosome 12q13 and are grouped into two distinct subfamilies based on structure similarity. One subfamily, consisting of KRTHB1, KRTHB3, and KRTHB6, is highly related. The other less-related subfamily includes KRTHB2, KRTHB4, and KRTHB5. All hair keratins are expressed in the hair follicle; this hair keratin, as well as KRTHB1 and KRTHB3, is found primarily in the hair cortex. Mutations in this gene and KRTHB1 have been observed in patients with a rare dominant hair disease, monilethrix. [provided by RefSeq]
LocationChromosome: 12   Locus: 12q13
Gene position52695649 - 52702947  Map Viewer
Gene orientationplus
Gene size7299 bp
Gene sequence
OMIM ID601928