FOSB wt Allele

Preferred Label : FOSB wt Allele;

NCIt synonyms : FOSB; GOSB; FosB Proto-Oncogene, AP-1 Transcription Factor Subunit wt Allele; GOS3; FBJ Murine Osteosarcoma Viral Oncogene Homolog B Gene; MGC42291; DKFZp686C0818; v-Fos FBJ Murine Osteosarcoma Viral Oncogene Homolog B Gene; AP-1; G0S3;

NCIt definition : Human FOSB wild-type allele is located in the vicinity of 19q13.32 and is approximately 7 kb in length. This allele, which encodes fosB protein, plays a role in the suppression of transcription by RNA polymerase II.;

GenBank Accession Number : NM_006732;

Détails

Origin ID

C52889;

UMLS CUI

C1705124;

Automatic exact mappings (from CISMeF team)
- Fosb protooncogene, ap1 transcription factor subunit [OMIM gene]
OMIM relation
- Fosb protooncogene, ap1 transcription factor subunit [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_has_physical_location
- 19: 50663093-50670276 [NCIt concept]
gene_in_chromosomal_location
- 19q13.32 [NCIt concept]
gene_involved_in_pathogenesis_of_disease
- Pseudomyogenic Hemangioendothelioma [NCIt concept]
gene_is_element_in_pathway
- FosB Drug-induction Pathway [NCIt concept]
gene_plays_role_in_process
- DNA Binding [NCIt concept]
- Transcriptional Regulation [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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