MDS2 wt Allele

Preferred Label : MDS2 wt Allele;

NCIt synonyms : RP11-223J15.1; Myelodysplastic Syndrome 2 Translocation Associated wt Allele;

NCIt definition : Human MDS2 wild-type allele is located in the vicinity of 1p36 and is approximately 59 kb in length. This allele, which encodes myelodysplastic syndrome 2 translocation-associated protein, is involved in a chromosomal translocation t(1;12)(p36.1;p13) with the ETV6 gene that is associated with myelodysplastic syndrome.;

NCIt note : EntrezGene classifies the MDS2 gene as Gene type miscRNA.;

GenBank Accession Number : AJ310434;

Details

Origin ID

C97616;

UMLS CUI

C3273521;

OMIM relation
- Mds2 gene [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
- 1p36 [NCIt concept]

Keyword's position in hierarchy(ies) :

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