ELL wt Allele - CISMeF

Preferred Label : ELL wt Allele;

NCIt synonyms : Men; ELL1; DKFZp434I1916; ELL Gene (11-19 Lysine-Rich Leukemia Gene) Gene; Chromosome 19 Open Reading Frame 17 Gene; Elongation Factor RNA Polymerase II wt Allele; C19orf17;

NCIt definition : Human ELL wild-type allele is located in the vicinity of 19p13.1 and is approximately 79 kb in length. This allele, which encodes RNA polymerase II elongation factor ELL protein, plays a role in the elongation of transcribed RNA. A chromosomal translocation t(11;19)(q23;p13.1) of this gene and the MLL gene is associated with acute myeloid leukemia.;

GenBank Accession Number : U16282;

Details

Origin ID

C97517;

UMLS CUI

C3273465;

Automatic exact mappings (from CISMeF team)
- Men [HPMULTI term]
- Men [UNESCO concept]
- Meningococcal vaccine, unspecified [UNVA Valence]
- Multiple endocrine neoplasia, type I [OMIM Phenotype]
- Multiple polyglandular tumours [ICD-11 Subcategory]
- Polyglandular activity in multiple endocrine adenomatosis (disorder) [SNOMED CT concept]
- humans [MeSH Descriptor]
- men [MeSH concept]
- men [MedlinePlus Group]
False automatic mappings
- Multiple endocrine neoplasia [ORDO Disease]
- men [MeSH Descriptor]
OMIM relation
- Elongation factor rna polymerase II [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 19p13.1 [NCIt concept]
gene_plays_role_in_process
- Transcription Elongation [NCIt concept]
- Transcriptional Regulation [NCIt concept]

Keyword's position in hierarchy(ies) :

Main resources

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