KRT5
From Wikipedia, the free encyclopedia
The human keratin 5 gene (KRT5) is a gene of 2301 base pairs (in the mRNA) that encodes proteins. A missense mutation in this gene can cause the disease Epidermolysis bullosa. KRT5 is on chromosome 12.
The human keratin 5 gene (KRT5) is a gene of 2301 base pairs (in the mRNA) that encodes proteins. A missense mutation in this gene can cause the disease Epidermolysis bullosa. KRT5 is on chromosome 12.