DNM1L wt Allele

Preferred Label : DNM1L wt Allele;

NCIt synonyms : S. cerevisiae DNM1/VPS1-Like Protein Gene; DRP1; DYMPLE; Dynamin Family Member, Proline-Rich C-Terminal Domain Less Gene; DVLP; EMPF; HDYNIV; Dynamin 1-Like wt Allele; DLP1;

NCIt definition : Human DNM1L wild-type allele is located in the vicinity of 12p11.21 and is approximately 66 kb in length. This allele, which encodes dynamin-1-like protein, is involved in the division process of both mitochondria and peroxisomes. Mutation of the gene is associated with lethal encephalopathy due to defective mitochondrial peroxisomal fission.;

GenBank Accession Number : AF000430;

Details

Origin ID

C116996;

UMLS CUI

C3889148;

Automatic exact mappings (from CISMeF team)
- Collapsin response mediator protein 1 [OMIM gene]
- Death-associated protein kinase 2 [OMIM gene]
- Dynamin 1-like [OMIM gene]
- Prenyl diphosphate synthase, subunit 2 [OMIM gene]
- Utrophin [OMIM gene]
- dynamin 1 like [ORDO Gene]
- utrophin [MeSH Descriptor]
OMIM relation
- Dynamin 1-like [OMIM gene]
See also inter- (CISMeF)
- Encephalopathy due to defective mitochondrial and peroxisomal fission 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_plays_role_in_process
- Apoptosis [NCIt concept]
- Endocytotic Process [NCIt concept]
- GTP Binding [NCIt concept]
- Hydrolysis [NCIt concept]
- Ligand Binding [NCIt concept]
- Transport Process [NCIt concept]

Keyword's position in hierarchy(ies) :

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