H3-3B wt Allele

Preferred Label : H3-3B wt Allele;

NCIt synonyms : H3 Histone, Family 3B Gene; H3.3B; H3 Histone, Family 3B (H3.3B) Gene; H3F3B; H3.3 Histone B wt Allele; H3 Histone Family Member 3B Gene;

NCIt related terms : H3F3B wt Allele;

NCIt definition : Human H3-3B wild-type allele is located in the vicinity of 17q25.1 and is approximately 9 kb in length. This allele, which encodes histone H3.3 protein, is involved in nucleosomal structure.;

NCIt note : Somatic mutation of the H3F3A gene may be associated with diffuse intrinsic pontine glioma. (Nature Genetics. 2012; 44:251-253.);

GenBank Accession Number : Z48950;

Details

Origin ID

C113761;

UMLS CUI

C3815142;

Automatic exact mappings (from CISMeF team)
- H3 histone, family 3b [OMIM gene]
OMIM relation
- H3 histone, family 3b [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_is_element_in_pathway
- Systemic Lupus Erythematosus Pathway [NCIt concept]
gene_plays_role_in_process
- Chromatin Remodeling [NCIt concept]
- Chromatin Structural Process [NCIt concept]
- Coagulation Process [NCIt concept]
- Gene Regulation Process [NCIt concept]

Keyword's position in hierarchy(ies) :

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