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Disease Info Card
Weaver Syndrome
Information about Weaver 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 Weaver Syndrome
Most recent studies have shown that Weaver Syndrome shares some biological mechanisms with abnormal-degeneration, bone-diseases-developmental, bovine-progressive-degenerative-myeloencephalopathy, cattle-diseases, congenital-abnormality, congenital-camptodactyly, congenital-foot-deformity, congenital-hand-deformities, congenital-hypothyroidism, craniofacial-abnormalities, developmental-delay-(disorder), developmental-disabilities, growth-disorders, hoarseness, macrocephaly, micrognathism, neoplasms, sotos-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Weaver Syndrome, and have been seen in publications frequently: Bone Maturation, Genetic Imprinting, Histone Modification, Pathogenesis, Phagocytosis, Transport
Quite a number of genes have been found to play important roles in Weaver Syndrome, such as ASXL1, ATP6V0A2, CDKN2A, CPM, ELN, EP300, EZH2, GPC3, INVS, KCNJ6, MFN2, NF1, NSD1, NUP98, PES1, PGR, TH. 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 Weaver Syndrome
This information is being compiled and will come in a future update
| Bone Maturation | Genetic Imprinting | Histone Modification |
| Pathogenesis | Phagocytosis | Transport |