t(3;14)(p14.1;q32)

Preferred Label : t(3;14)(p14.1;q32);

NCIt synonyms : t 3 14 p14 1 q32;

NCIt definition : A chromosomal translocation involving breakpoints within the p14.1 band on the short arm of chromosome 3 and the q32 band on the long arm of chromosome 14. This rearrangement is associated with aberrant expression of the FOXP1 gene and extranodal mucosa-associated lymphoid tissue (MALT) lymphoma.;

PubMed : 15703784;

Details

Origin ID

C44521;

UMLS CUI

C1711150;

Semantic type(s)
- Cell or Molecular Dysfunction [UMLS semantic type]
cytogenetic_abnormality_involves_chromosome
- Human Chromosome 14 [NCIt concept]
- Human Chromosome 3 [NCIt concept]
may_be_cytogenetic_abnormality_of_disease
- Borrelia Burgdoferi-Associated Primary Cutaneous Marginal Zone Lymphoproliferative Disorder [NCIt concept]
- Chlamydia Psittaci-Associated Ocular Adnexal Mucosa-Associated Lymphoid Tissue Lymphoma [NCIt concept]
- Conjunctival Mucosa-Associated Lymphoid Tissue Lymphoma [NCIt concept]
- Lacrimal Drainage System Mucosa-Associated Lymphoid Tissue Lymphoma [NCIt concept]
- Lacrimal Gland Mucosa-Associated Lymphoid Tissue Lymphoma [NCIt concept]
- Lacrimal System Mucosa-Associated Lymphoid Tissue Lymphoma [NCIt concept]
- Ocular Adnexal Mucosa-Associated Lymphoid Tissue Lymphoma [NCIt concept]
- Primary Cutaneous Marginal Zone Lymphoproliferative Disorder [NCIt concept]
- Thyroid Gland Mucosa-Associated Lymphoid Tissue Lymphoma [NCIt concept]
molecular_abnormality_involves_gene
- FOXP1 Gene [NCIt concept]
- Immunoglobulin Heavy Component Gene [NCIt concept]

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