KDM3B wt Allele

Preferred Label : KDM3B wt Allele;

NCIt synonyms : Chromosome 5 Open Reading Frame 7; JMJD1B; 5qNCA; KIAA1082; NET22; Lysine Demethylase 3B wt Allele; C5orf7; DIJOS;

NCIt definition : Human KDM3B wild-type allele is located in the vicinity of 5q31.2 and is approximately 84 kb in length. This allele, which encodes lysine-specific demethylase 3B protein, is involved in histone demethylation. Mutation of the gene is associated with Diets-Jongmans syndrome and interstitial deletion of 5q is associated with myeloid leukemia and myelodysplasia.;

NCI Metathesaurus CUI : CL1643025;

GenBank Accession Number : AF251039;

Details

Origin ID

C177187;

UMLS CUI

C5443956;

Automatic exact mappings (from CISMeF team)
- Diets-jongmans syndrome [OMIM Phenotype]
- Lysine demethylase 3b [OMIM gene]
OMIM relation
- Lysine demethylase 3b [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_plays_role_in_process
- Chromatin Remodeling [NCIt concept]
- Histone Demethylation [NCIt concept]
- Oxidation [NCIt concept]
- Oxidation/Reduction [NCIt concept]
- Transcriptional Regulation [NCIt concept]

Keyword's position in hierarchy(ies) :

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