KRT13 wt Allele

Preferred Label : KRT13 wt Allele;

NCIt synonyms : MGC161462; K13; Keratin 13 wt Allele; MGC3781; CK13;

NCIt definition : Human KRT13 wild-type allele is located in the vicinity of 17q21.2 and is approximately 5 kb in length. This allele, which encodes keratin, type I cytoskeletal 13 protein, plays a role in epidermal development. Mutation of the gene is associated with white sponge nevus.;

GenBank Accession Number : NM_153490;

Details

Origin ID

C107626;

UMLS CUI

C3810567;

Automatic exact mappings (from CISMeF team)
- Keratin 13, type I [OMIM gene]
- keratin 13 [ORDO Gene]
OMIM relation
- Keratin 13, type I [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 17q21.2 [NCIt concept]
gene_plays_role_in_process
- Cell Movement Process [NCIt concept]
- Cytoskeletal Process [NCIt concept]
- Keratinization [NCIt concept]
- Protein-Protein Interaction [NCIt concept]
- Regulation of Cell Shape [NCIt concept]

Keyword's position in hierarchy(ies) :

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