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Disease Info Card
Single Gene Defect
Information about Single Gene Defect: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Single Gene Defect
Most recent studies have shown that Single Gene Defect shares some biological mechanisms with aneuploidy, autoimmune-diseases, autoimmune-reaction, autoimmunity, congenital-abnormality, congenital-heart-defects, cystic-fibrosis, cytogenetic-abnormality, diabetes-mellitus, diabetes-mellitus-non-insulin-dependent, fibrosis, genetic-diseases-inborn, heart-diseases, hereditary-diseases, immunologic-deficiency-syndromes, infective-disorder, malignant-neoplasms, neoplasms, obesity.
Among the many pathways, these few ones have gauged particular interests from scientists studying Single Gene Defect, and have been seen in publications frequently: Aging, Brain Development, Cell Adhesion, Cell Cycle, Coagulation, Dna Amplification, Dna Repair, Endocytosis, Fertilization, Glomerular Filtration, Immune Response, Localization, Oocyte Growth, Pathogenesis, Regulation Of Gene Expression, Secretion, Sex Determination, Spermatogenesis, Transport, Transposition
Quite a number of genes have been found to play important roles in Single Gene Defect, such as ADO, CFTR, CYBB, FGF8, FGFR1, FMR1, HBB, HNF4A, IGF1, INS, LEP, MC4R, PGD, PHGDH, POMC, SLC11A1, SNCA, WAS. 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.