MeSH Browser

MeSH Supplementary: KRT1 protein, human
Unique ID: C491616
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C491616
Entry Term(s): Krt1-1 protein, human; keratin 1 (epidermolytic hyperkeratosis) protein, human; keratin 1 protein, human
Registry Numbers: 0
Previous Indexing: *KERATINS (2004-2006)
Heading Mapped to: *Keratin-1
Frequency: 120
Note: Mutations in the keratin K1 gene (KRT1) have been shown to underlie a variety of phenotypes typically involving generalized epidermolytic hyperkeratosis, but in some cases the phenotype can be more regionally restricted; RefSeq NM_006121
Source: Br J Dermatol. 2004 Jun;150(6):1096-103
Date of Entry: 2004/10/05
Revision Date: 2006/08/04

Concept UI: M0473537
Registry Numbers: 0
Terms: KRT1 protein, human Preferred Term
Term UI T665576
Date02/01/2006
LexicalTag NON
ThesaurusID NLM (2006); keratin 1 (epidermolytic hyperkeratosis) protein, human
Term UI T665577
Date02/01/2006
LexicalTag NON
ThesaurusID NLM (2006); keratin 1 protein, human
Term UI T612064
Date10/05/2004
LexicalTag NON
ThesaurusID NLM (2004); Krt1-1 protein, human
Term UI T612065
Date10/05/2004
LexicalTag NON
ThesaurusID NLM (2004)

KRT1 protein, human MeSH Supplementary Concept Data 2025