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Disease Info Card
Low Set Ears
Information about Low Set Ears: 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 Low Set Ears
Most recent studies have shown that Low Set Ears shares some biological mechanisms with cleft-palate, congenital-abnormality, congenital-heart-defects, craniofacial-abnormalities, cytogenetic-abnormality, developmental-delay-(disorder), dwarfism, dysplasia, fetal-growth-retardation, growth-retardation, hypoplasia, microcephaly, micrognathism, monosomy, muscle-hypotonia, orbital-separation-excessive, partial-trisomy, trisomy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Low Set Ears, and have been seen in publications frequently: Aging, Bone Maturation, Brain Development, Cell Migration, Fertilization, Hypersensitivity, Interphase, Keratinization, Localization, Meiosis, Meiosis I, Meiosis Ii, Metaphase, Neural Crest Cell Migration, Ossification, Oxidative Phosphorylation, Pathogenesis, Pigmentation, Sex Determination, Transposition
Quite a number of genes have been found to play important roles in Low Set Ears, such as CDK5R1, CDKN2B, CHP1, ENDOU, EXOSC6, INS, INVS, LMLN, MRPL28, NXT1, PTGES3, RRAS, S100A10, SS18L1, SUB1, TMED10, TPPP, TWIST1. 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.