KRT86
keratin 86
Normal Function
Health Conditions Related to Genetic Changes
Monilethrix
Several mutations in the KRT86 gene can cause monilethrix, a hair condition characterized by strands of hair with a beaded appearance and short, brittle hair that breaks easily. Mutations associated with this condition change a single protein building block (amino acid) in the K86 protein. The amino acid changes usually occur in a region of the K86 protein thought to be important in intermediate filament formation. In people with monilethrix, the cortex of the affected hair shaft appears abnormal. However, it is unclear how mutations in the KRT86 gene are related to the abnormality in the cortex or the beaded appearance of the hair.
More About This Health ConditionRelated Conditions
Monilethrix
Health Conditions Related to Genetic Changes
Several mutations in the KRT86 gene can cause monilethrix, a hair condition characterized by strands of hair with a beaded appearance and short, brittle hair that breaks easily. Mutations associated with this condition change a single protein building block (amino acid) in the K86 protein. The amino acid changes usually occur in a region of the K86 protein thought to be important in intermediate filament formation. In people with monilethrix, the cortex of the affected hair shaft appears abnormal. However, it is unclear how mutations in the KRT86 gene are related to the abnormality in the cortex or the beaded appearance of the hair.