H2AB1 wt Allele

Preferred Label : H2AB1 wt Allele;

NCIt synonyms : H2A.Bbd; H2A Histone Family, Member B1 Gene; H2A.B Variant Histone 1 wt Allele; H2A.B; H2AFB1; H2A Histone Family Member B1 Gene;

NCIt definition : Human H2AB1 wild-type allele is located in the vicinity of Xq28 and is approximately 1 kb in length. This allele, which encodes histone H2A-Bbd type 1 protein, is involved in the modulation of DNA compaction, which regulates gene transcription and mRNA processing.;

NCIt note : The H2AFB1 gene is is 98% identical to the H2AFB2 and H2AFB3 genes. (OMIM);

NCI Metathesaurus CUI : CL555432;

GenBank Accession Number : NM_001017990;

Details

Origin ID

C154650;

UMLS CUI

C4723765;

Automatic exact mappings (from CISMeF team)
- H2a.b variant histone 1 [OMIM gene]
- H2a.b variant histone 3 [OMIM gene]
OMIM relation
- H2a.b variant histone 1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- Xq28 [NCIt concept]
gene_is_element_in_pathway
- Systemic Lupus Erythematosus Pathway [NCIt concept]
gene_plays_role_in_process
- Chromatin Structural Process [NCIt concept]
- DNA Topology Regulation [NCIt concept]
- Gene Regulation Process [NCIt concept]
- RNA Processing [NCIt concept]
- Transcriptional Activation [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients