KRT86

Keratin 86
Identifiers
Symbols	KRT86 ; HB6; KRTHB1; Hb1; KRTHB6; MNX; hHb6
External IDs	Template:OMIM5 Template:MGI HomoloGene: 1717
Gene ontology Molecular function Template:GNF GO Cellular component Template:GNF GO Biological process Template:GNF GO
Orthologs
Template:GNF Ortholog box
Species	Human	Mouse
Entrez	n/a	n/a
Ensembl	n/a	n/a
UniProt	n/a	n/a
RefSeq (mRNA)	n/a	n/a
RefSeq (protein)	n/a	n/a
Location (UCSC)	n/a	n/a
PubMed search	n/a	n/a

Keratin 86, also known as KRT86, is a human gene.

The 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.

Further reading

• Langbein L, Schweizer J (2005). "Keratins of the human hair follicle". Int. Rev. Cytol. 243: 1–78. doi:10.1016/S0074-7696(05)43001-6. PMID 15797458.
• Rogers MA, Nischt R, Korge B; et al. (1995). "Sequence data and chromosomal localization of human type I and type II hair keratin genes". Exp. Cell Res. 220 (2): 357–62. doi:10.1006/excr.1995.1326. PMID 7556444.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Rogers MA, Langbein L, Praetzel S; et al. (1997). "Sequences and differential expression of three novel human type-II hair keratins". Differentiation. 61 (3): 187–94. PMID 9084137.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Winter H, Rogers MA, Langbein L; et al. (1997). "Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix". Nat. Genet. 16 (4): 372–4. doi:10.1038/ng0897-372. PMID 9241275.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Winter H, Rogers MA, Gebhardt M; et al. (1998). "A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix". Hum. Genet. 101 (2): 165–9. PMID 9402962.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Bowden PE, Hainey SD, Parker G; et al. (1998). "Characterization and chromosomal localization of human hair-specific keratin genes and comparative expression during the hair growth cycle". J. Invest. Dermatol. 110 (2): 158–64. doi:10.1046/j.1523-1747.1998.00097.x. PMID 9457912.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Winter H, Clark RD, Tarras-Wahlberg C; et al. (1999). "Monilethrix: a novel mutation (Glu402Lys) in the helix termination motif and the first causative mutation (Asn114Asp) in the helix initiation motif of the type II hair keratin hHb6". J. Invest. Dermatol. 113 (2): 263–6. doi:10.1046/j.1523-1747.1999.00685.x. PMID 10469314.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Korge BP, Hamm H, Jury CS; et al. (1999). "Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotype". J. Invest. Dermatol. 113 (4): 607–12. doi:10.1046/j.1523-1747.1999.00722.x. PMID 10504448.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Pearce EG, Smith SK, Lanigan SW, Bowden PE (2000). "Two different mutations in the same codon of a type II hair keratin (hHb6) in patients with monilethrix". J. Invest. Dermatol. 113 (6): 1123–7. doi:10.1046/j.1523-1747.1999.00777.x. PMID 10594761.CS1 maint: Multiple names: authors list (link)
• Rogers MA, Winter H, Langbein L; et al. (2000). "Characterization of a 300 kbp region of human DNA containing the type II hair keratin gene domain". J. Invest. Dermatol. 114 (3): 464–72. doi:10.1046/j.1523-1747.2000.00910.x. PMID 10692104.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Strausberg RL, Feingold EA, Grouse LH; et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Gerhard DS, Wagner L, Feingold EA; et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMID 15489334.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)
• Schweizer J, Bowden PE, Coulombe PA; et al. (2006). "New consensus nomenclature for mammalian keratins". J. Cell Biol. 174 (2): 169–74. doi:10.1083/jcb.200603161. PMID 16831889.CS1 maint: Explicit use of et al. (link) CS1 maint: Multiple names: authors list (link)