KRT35
Description
The KRT35 (keratin 35) is a protein-coding gene located on chromosome 17.
Keratin, type I cuticular Ha5 is a keratin protein that in humans is encoded by the KRT35 gene.
KRT35 is also known as HA5, Ha-5, K35, KRTHA5, hHa5.
Associated Diseases
- ovarian cancer
- thyroid gland adenocarcinoma
- esophageal cancer
- low grade glioma
- Gorham-Stout disease
- Griscelli syndrome type 3
- uncombable hair syndrome
- melorheostosis
- oculocutaneous albinism type 3
- microcephaly-albinism-digital anomalies syndrome
- Tietz syndrome
- ermine phenotype
