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Disease Info Card
Kniest Dysplasia
Information about Kniest Dysplasia: 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 Kniest Dysplasia
Most recent studies have shown that Kniest Dysplasia shares some biological mechanisms with achondroplasia, bone-diseases-developmental, cataract, cleft-palate, dwarfism, dysplasia, eye-abnormalities, hypoplasia, mucopolysaccharidoses, myopia, osteochondrodysplasias, retinal-detachment, skeletal-dysplasia, spondyloepiphyseal-dysplasia, spondyloepiphyseal-dysplasia-congenita, stickler-syndrome-(disorder), thanatophoric-dysplasia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Kniest Dysplasia, and have been seen in publications frequently: Cell Division, Collagen Fibril Organization, Excretion, Fibril Organization, Ossification, Pathogenesis, Proteolysis, Rna Splicing, Secretion, Segmentation
Quite a number of genes have been found to play important roles in Kniest Dysplasia, such as AKR1C2, ARHGAP4, CALML3, COL2A1, COMP, CP, FABP6, FMOD, GDI1, HNRNPC, HSPG2, IK, ITGA2B, ITGB3, RFC1, RFC2, SS18L1, TNIP1. 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.
Pathways Related to Kniest Dysplasia
This information is being compiled and will come in a future update
| Cell Division | Collagen Fibril Organization | Excretion |
| Fibril Organization | Ossification | Pathogenesis |
| Proteolysis | Rna Splicing | Secretion |
| Segmentation |