Keratin 17

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KRT17
Identifiers
AliasesKRT17, K17, PC, PC2, PCHC1, 39.1, CK-17, keratin 17
External IDsOMIM: 148069; MGI: 96691; HomoloGene: 363; GeneCards: KRT17; OMA:KRT17 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000422

NM_010663

RefSeq (protein)

NP_000413

NP_034793

Location (UCSC)Chr 17: 41.62 – 41.62 MbChr 11: 100.15 – 100.15 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Keratin 17, also known as KRT17, is a human gene.[5]

Keratin 17 is a type I cytokeratin. It is found in nail beds, hair follicles, sebaceous glands, and other epidermal appendages. Mutations in the gene encoding this protein lead to Jackson-Lawler type pachyonychia congenita and steatocystoma multiplex.[5]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000128422Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000035557Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b "Entrez Gene: KRT17 keratin 17".

Further reading