Keratin 1
Appearance
Keratin 1 is a member of the keratin family. It is specifically expressed in the spinous and granular layers of the epidermis with family member keratin 10. Mutations in this gene have been associated with the variants of bullous congenital ichthyosiform erythroderma in which the palms and soles of the feet are affected.
Interactions
Keratin 1 has been shown to interact with Desmoplakin[5] and PRKCE.[6]
See also
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000167768 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000046834 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ Meng, J J; Bornslaeger E A; Green K J; Steinert P M; Ip W (Aug 1997). "Two-hybrid analysis reveals fundamental differences in direct interactions between desmoplakin and cell type-specific intermediate filaments". J. Biol. Chem. 272 (34). UNITED STATES: 21495–503. doi:10.1074/jbc.272.34.21495. ISSN 0021-9258. PMID 9261168.
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(help)CS1 maint: unflagged free DOI (link) - ^ England, Karen; Ashford David; Kidd Daniel; Rumsby Martin (Jun 2002). "PKC epsilon is associated with myosin IIA and actin in fibroblasts". Cell. Signal. 14 (6). England: 529–36. doi:10.1016/S0898-6568(01)00277-7. ISSN 0898-6568. PMID 11897493.
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Further reading