NIN wt Allele - CISMeF

Preferred Label : NIN wt Allele;

NCIt synonyms : KIAA1565; Ninein wt Allele; Ninein Centrosomal Protein Gene; SCKL7; Ninein (GSK3B Interacting Protein) Gene;

NCIt definition : Human NIN wild-type allele is located in the vicinity of 14q22.1 and is approximately 111 kb in length. This allele, which encodes ninein protein, plays a role in the modulation of centrosome structure. A chromosomal translocation t(5;14)(q33;q24) of this gene and the PDGFRB is associated with chronic myeloproliferative disorder with eosinophilia.;

GenBank Accession Number : AF212162;

Details

Origin ID

C97669;

UMLS CUI

C3273558;

Automatic exact mappings (from CISMeF team)
- Ninein [OMIM gene]
- Seckel syndrome 7 [DO Concept]
- Seckel syndrome 7 [OMIM Phenotype]
OMIM relation
- Ninein [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_plays_role_in_process
- Ligand Binding [NCIt concept]
- Protein-Protein Interaction [NCIt concept]

Keyword's position in hierarchy(ies) :

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