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Disease Info Card
Acrorenoocular Syndrome
Information about Acrorenoocular Syndrome: 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 Acrorenoocular Syndrome
Most recent studies have shown that Acrorenoocular Syndrome shares some biological mechanisms with complete-hearing-loss, congenital-hand-deformities, congenital-heart-defects, duane-retraction-syndrome, eye-abnormalities, facial-asymmetry, fetal-diseases, fetal-growth-retardation, haploinsufficiency, heart-septal-defects, holt-oram-syndrome, hypoplasia, limb-defect, limb-deformities-congenital, ocular-motility-disorders, ophthalmoplegia, sensorineural-hearing-loss-(disorder), strabismus, townes-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Acrorenoocular Syndrome, and have been seen in publications frequently: Cell Cycle, Cell Fate Specification, Cell Proliferation, Fin Development, G1 Phase, Heart Development, Innervation, Kidney Development, Limb Development, Neural Tube Closure, Neurogenesis, Pathogenesis, Pectoral Fin Development, Regeneration, S Phase, Stem Cell Proliferation, Tube Closure
Quite a number of genes have been found to play important roles in Acrorenoocular Syndrome, such as BMP4, CD40, CUX1, DPM1, FBXW11, HDAC9, KIF21A, MID1, SALL1, SALL2, SALL4, SLC22A3, STS, TBX5, TPX2. 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.