KRT86

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

The KRT86 gene encodes for keratin, type II cuticular Hb6 protein in humans.[5][6][7]

AliasesKRT86, HB6, Hb1, KRTHB1, KRTHB6, MNX, hHb6, K86, keratin 86
End52,309,163 bp[1]
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KRT86
Identifiers
AliasesKRT86, HB6, Hb1, KRTHB1, KRTHB6, MNX, hHb6, K86, keratin 86
External IDsOMIM: 601928; MGI: 109362; HomoloGene: 1717; GeneCards: KRT86; OMA:KRT86 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002284
NM_001320198

NM_010667

RefSeq (protein)

NP_001307127

NP_034797

Location (UCSC)Chr 12: 52.25 – 52.31 MbChr 15: 101.37 – 101.38 Mb
PubMed search[3][4]
Wikidata
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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 KRT81, KRT83, and KRT86, is highly related. The other, less-related subfamily includes KRT82, KRT84, and KRT85. All hair keratins are expressed in the hair follicle; this hair keratin, as well as KRT81 and KRT83, is found primarily in the hair cortex. Mutations in this gene and KRT81 have been observed in patients with a rare dominant hair disease, monilethrix.[7]

References

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