WDR62 | bioCADDIE Data Discovery Index
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Displaying 3 of 3 results for "WDR62"
  1. C3H62_ARATH UniProt:Swiss-Prot

    ID: Q9FE91

    Description: Zinc finger CCCH domain-containing protein 62 WD 1 WD 2 WD 3

  2. Whole-genome sequencing identifies frequent mutations of microcephaly-associated genes in autism : WGS of chinisese ASD subjects BioProject

    ID: PRJEB18551

    Keywords: Other

    Access Type: download

    dataset.description: s of several microcephaly-associated genes (ASPM, WDR62, and ZNF335) were found in ASD. In chromosomal structure analyses, we found four de novo CNVs and one de novo chromosomal rearrangement event, including a de novo duplication of UBE3A-containing region at 15q11.2-q13.1, which causes Angelman syndrome and microcephaly, and a disrupted TNR due to de novo chromosomal translocation t(1;5)(q25.1;q33.2). Taken together, our results suggest that abnormalities of centrosomal function and chromatin remodeling of the microcephaly-associated genes are actively implicated in pathogenesis of ASD....
  3. WDR62_PIG UniProt:Swiss-Prot

    ID: Q8HXL3

    Description: Removed WD repeat-containing protein 62 WD 1 WD 2 WD

Displaying 3 of 3 results for "WDR62"