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Open Access Articles- Top Results for Keratin 13

Keratin 13

Template:Infobox3cols/rowTemplate:Infobox3cols/rowTemplate:Infobox3cols/rowTemplate:Infobox3cols/row
Identifiers
SymbolsKRT13 ; CK13; K13
External IDsOMIM148065 MGI101925 HomoloGene40740 GeneCards: KRT13 Gene
Orthologs
SpeciesHumanMouse
Entrez386016663
EnsemblENSG00000171401ENSMUSG00000044041
UniProtP13646P08730
RefSeq (mRNA)NM_002274NM_010662
RefSeq (protein)NP_002265NP_034792
Location (UCSC)Chr 17:
39.66 – 39.66 Mb
Chr 11:
100.12 – 100.12 Mb
PubMed search[1][2]

Keratin 13 (or cytokeratin 13) is a protein that in humans is encoded by the KRT13 gene.[1][2]

Keratin 13 is a type I cytokeratin, it is paired with keratin 4 and found in the suprabasal layers of non-cornified stratified epithelia. Mutations in the gene encoding this protein and keratin 4 have been associated with the autosomal dominant disorder White Sponge Nevus.[3]

K13 is negative in buccal epithelium.[citation needed]

References

  1. ^ Romano V, Raimondi E, Bosco P, Feo S, Di Pietro C, Leube RE, Troyanovsky SM, Ceratto N (October 1992). "Chromosomal mapping of human cytokeratin 13 gene (KRT13)". Genomics 14 (2): 495–7. PMID 1385306. doi:10.1016/S0888-7543(05)80250-2. 
  2. ^ Schweizer J, Bowden PE, Coulombe PA, Langbein L, Lane EB, Magin TM, Maltais L, Omary MB, Parry DA, Rogers MA, Wright MW (July 2006). "New consensus nomenclature for mammalian keratins". J. Cell Biol. 174 (2): 169–74. PMC 2064177. PMID 16831889. doi:10.1083/jcb.200603161. 
  3. ^ Richard G, De Laurenzi V, Didona B, Bale SJ, Compton JG (December 1995). "Keratin 13 point mutation underlies the hereditary mucosal epithelial disorder white sponge nevus". Nat. Genet. 11 (4): 453–5. PMID 7493031. doi:10.1038/ng1295-453. 

Further reading

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