MYO1E wt Allele

Preferred Label : MYO1E wt Allele;

NCIt synonyms : MGC104638; Myosin IC Gene; MYO1C; HuncM-IC; FSGS6; Myosin IE wt Allele;

NCIt definition : Human MYO1E wild-type allele is located in the vicinity of 15q22.2 and is approximately 240 kb in length. This allele, which encodes unconventional myosin-Ie protein, is involved in the transport of lipids and cytoplasmic vesicles. Mutation of the gene is associated with focal segmental glomerulosclerosis type 6.;

NCI Metathesaurus CUI : CL522229;

GenBank Accession Number : U14391;

Details

Origin ID

C134692;

UMLS CUI

C4521509;

Automatic exact mappings (from CISMeF team)
- Focal segmental glomerulosclerosis 6 [OMIM Phenotype]
- Myosin ic [OMIM gene]
- Myosin ie [OMIM gene]
- focal segmental glomerulosclerosis 6 [DO Concept]
- myosin IC [ORDO Gene]
- myosin IE [ORDO Gene]
OMIM relation
- Myosin ie [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 15q22.2 [NCIt concept]
gene_plays_role_in_process
- Cell Movement Process [NCIt concept]
- Cytoskeletal Process [NCIt concept]
- Intracellular Transport [NCIt concept]
- Lipid Transport [NCIt concept]
- Regulation of Cell Shape [NCIt concept]

Keyword's position in hierarchy(ies) :

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