KRT6A wt Allele

Preferred Label : KRT6A wt Allele;

NCIt synonyms : Keratin, Type II Cytoskeletal 6A Gene; CK6A; CK6C; CK6D; Keratin 6D Gene; Keratin 6A, Type II Gene; KB6; Cytokeratin 6C Gene; Cytokeratin 6A Gene; CK-6C; CK-6E; K6A; K6C; Keratin 6C Gene; K6D; KRT6C; Keratin, Epidermal Type II, K6A Gene; KRT6D; Keratin 6A wt Allele; PC3; Cytokeratin 6D Gene;

NCIt definition : Human KRT6A wild-type allele is located in the vicinity of 12q13.13 and is approximately 6 kb in length. This allele, which encodes keratin, type II cytoskeletal 6A protein, plays a role in the activation of follicular keratinocytes after wounding. Mutation of the gene is associated with pachyonychia congenita 3.;

NCI Metathesaurus CUI : CL1799034;

GenBank Accession Number : BC014152;

Details

Origin ID

C190242;

UMLS CUI

C5781379;

Automatic exact mappings (from CISMeF team)
- B-cell antiproliferation factor 2 [OMIM gene]
- Chromobox 8 [OMIM gene]
- Keratin 6c, type II [OMIM gene]
- PC3 (body structure) [SNOMED CT concept]
- Pachyonychia congenita 3 [OMIM Phenotype]
- Proprotein convertase, subtilisin/kexin-type, 1 [OMIM gene]
- parvocellular oculomotor nucleus [UBERON concept]
- proprotein convertase subtilisin/kexin type 1 [ORDO Gene]
OMIM relation
- Keratin 6a, type II [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
Validated automatic mappings to NTBT
- Keratin 6a, type II [OMIM gene]
- keratin 6A [ORDO Gene]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 12q13.13 [NCIt concept]
gene_plays_role_in_process
- Cell Movement Process [NCIt concept]
- Cytoskeletal Modeling [NCIt concept]
- Cytoskeletal Process [NCIt concept]
- Histogenic Process [NCIt concept]
- Keratinization [NCIt concept]
- Protein-Protein Interaction [NCIt concept]
- Regulation of Cell Shape [NCIt concept]
- Wound Repair [NCIt concept]

Keyword's position in hierarchy(ies) :

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