TNC wt Allele - CISMeF

Preferred Label : TNC wt Allele;

NCIt synonyms : HXB; GMEM; TN; DFNA56; TN-C; Tenascin C (Hexabrachion) Gene; JI; Hexabrachion (Tenascin C, Cytotactin) Gene; 150-225; GP; Hexabrachion (Tenascin) Gene; Deafness, Autosomal Dominant 56 Gene; Tenascin C wt Allele;

NCIt definition : Human TNC wild-type allele is located within 9q32-q34 and is approximately 98 kb in length. This allele, which encodes tenascin protein, is involved in extracellular matrix conformation.;

GenBank Accession Number : NM_002160;

Details

Origin ID

C52122;

UMLS CUI

C1705010;

False automatic mappings
- Witkop syndrome [OMIM Phenotype]
OMIM relation
- Tenascin C [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 9q33 [NCIt concept]
gene_is_element_in_pathway
- ECM-Receptor Interaction Signaling Pathway [NCIt concept]
- Focal Adhesion Pathway [NCIt concept]
gene_plays_role_in_process
- Cell Adhesion Process [NCIt concept]
- Cell Growth [NCIt concept]
- Cell Movement [NCIt concept]
- Cell-Matrix Adhesion Process [NCIt concept]
- Environment-to-Cell Communication [NCIt concept]
- Morphogenesis [NCIt concept]
- Organogenesis [NCIt concept]
- Protein-Protein Interaction [NCIt concept]
- Wound Repair [NCIt concept]

Keyword's position in hierarchy(ies) :

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