Chromosome 13q Deletion

Overview of Chromosome 13q Deletion

Most recent studies have shown that Chromosome 13q Deletion shares some biological mechanisms with chromosomal-deletion, chromosomal-translocation, chromosome-13q-deletion-syndrome, chronic-lymphocytic-leukemia, cytogenetic-abnormality, leukemia, loss-of-chromosome-11q, loss-of-chromosome-13, loss-of-chromosome-17p, loss-of-chromosome-20q, loss-of-chromosome-5q, lymphoid-leukemia, malignant-neoplasms, monosomy, multiple-myeloma, neoplasms, retinoblastoma, trisomy.

Among the many pathways, these few ones have gauged particular interests from scientists studying Chromosome 13q Deletion, and have been seen in publications frequently: Angiogenesis, Cell Cycle, Dna Repair, Drug Resistance, Enucleation, Interphase, Metaphase, Neural Tube Development, Pathogenesis, Reverse Transcription, Sensitization, Transposition, Tube Development

Quite a number of genes have been found to play important roles in Chromosome 13q Deletion, such as ASXL1, CCND1, CD38, CD55, CDKN1A, CDKN2A, HRAS, IL2, MID1, NT5E, NTS, PAFAH1B1, RB1, SF3B1, TP53, YWHAE, ZAP70, ZIC2. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.

Chromosome 13q Deletion Related Genes

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Pathways Related to Chromosome 13q Deletion

This information is being compiled and will come in a future update

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