GeneQuery™ Human Autism Spectrum Disorder qPCR Array Kit
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Further Information
Description:
ScienCell's GeneQuery™ Human Autism Spectrum Disorder qPCR Array Kit (GQH-ASD) profiles 88 key genes associated with autism spectrum disorder. Autism spectrum disorder is a developmental disability that can result in social, communication, behavioral, and learning challenges. The disease is early-appearing, with symptoms often presenting early in childhood, and evidence suggests there is a strong hereditary component. Below are brief examples of how included genes may be grouped according to their function:
- Neurodevelopment - : ADNP, ANKRD11, ARID1B, ASH1L, ASXL3, AUTS2, BCL11A, CACNA1H, CHD2, DISC1, DSCAM, FOXP1, GRIN2B, KATNAL2, KDM6B, KMT2C, MET, NCKAP1, NRXN3, PHF2, POGZ, RBFOX1, RELN, RIMS, SEMA5A, SHANK2, TCF4, ZBTB20
- Impaired - communication/behavioral ability - : CNTNAP2, FOXP2, GRIK2, KMT2A, KMT5B, MACROD2, MED13L, PAX5, PTEN, SHANK3, SPAST
- Social deficits/behavioral abnormalities: - AVPR1A, BCKDK, CNTNAP4, DIP2A, GRIP1, HMGN1
- Calcium signaling/calcium channels: - ATP2B2, CACNB2, CDC42BPB, PRKCB
- Altered expression linked to ASD: - ASTN2, CACNA2D3, CHD8, CHRNA7, CTCF, CTTNBP2, FOXP1, GABRB3, GPHN, GRIP1, KDM5B, MBD5, MYT1L, NLGN3, NR3C2, NRXN1, PTCHD1, SETBP1, SETD5, SYNGAP1, TBR1, TRIO, TRIP12, ZMYND11, WAC, WDFY3
- Novel variants found in ASD - : DEAF1, MAGEL2, TNRC6B, TRPC6
- Other risk factors for autism - : CACNA1D, CHD8, CTNND2, CUL3, MACROD2, MECP2, OXTR, SCN2A, SLC9A9
- Linked to non-syndromic autism - : ANK2, KMT2E, NLGN4X, TRPC6, SHANK3
Extra Description:
ScienCell's GeneQuery™ Human Autism Spectrum Disorder qPCR Array Kit (GQH-ASD) profiles 88 key genes associated with autism spectrum disorder.
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