VIM wt Allele - CISMeF

Preferred Label : VIM wt Allele;

NCIt synonyms : VIM; Vimentin wt Allele; HEL113; CTRCT30;

NCIt definition : Human VIM wild-type allele is located in the vicinity of 10p13 and is approximately 8 kb in length. This allele, which encodes vimentin protein, plays a role in the maintenance of the cellular structure of mesenchymal tissues.;

GenBank Accession Number : NM_003380.1;

Details

Origin ID

C52442;

UMLS CUI

C1704976;

Automatic exact mappings (from CISMeF team)
- Vimentin [OMIM gene]
- cataract 30 [DO Concept]
- vimentin [ORDO Gene]
OMIM relation
- Vimentin [OMIM gene]
See also inter- (CISMeF)
- Cataract 30, multiple types [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 10p13 [NCIt concept]
gene_plays_role_in_process
- Cell Movement Process [NCIt concept]
- Cytoskeletal Process [NCIt concept]
- Regulation of Cell Shape [NCIt concept]

Keyword's position in hierarchy(ies) :

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