DIS3L2 wt Allele

Preferred Label : DIS3L2 wt Allele;

NCIt synonyms : Family With Sequence Similarity 6, Member A Gene; DIS3 Mitotic Control, S. cerevisiae, Homolog-Like 2 Gene; DIS3 Like 3'-5' Exoribonuclease 2 wt Allele; FLJ36974; hDIS3L2; DIS3 Mitotic Control Homolog-Like 2 Gene; FAM6A; DIS3 Mitotic Control Homolog (S. cerevisiae)-Like 2 Gene; MGC42174; DIS3-Like 3-Prime-5-Prime Exoribonuclease 2 Gene; PRLMNS;

NCIt definition : Human DIS3L2 wild-type allele is located in the vicinity of 2q37.1 and is approximately 383 kb in length. This allele, which encodes DIS3-like exonuclease 2 protein, plays a role in exosome-independent RNA degradation. Mutation of the gene is associated with Perlman syndrome.;

NCI Metathesaurus CUI : CL1643103;

GenBank Accession Number : BC026166;

Details

Origin ID

C177172;

UMLS CUI

C5443954;

Automatic exact mappings (from CISMeF team)
- DIS3 like 3'-5' exoribonuclease 2 [ORDO Gene]
- Perlman syndrome [OMIM Phenotype]
OMIM relation
- Dis3-like 3-prime-5-prime exoribonuclease 2 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 2q37.1 [NCIt concept]
gene_plays_role_in_process
- Hydrolysis [NCIt concept]
- RNA Degradation [NCIt concept]
- RNA Processing [NCIt concept]

Keyword's position in hierarchy(ies) :

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