QuickView for XM_001162664 (gene)

1. WDR62-deficiency Causes Autism-like Behaviors Independent of Microcephaly in Mice.
2. WDR62 variants contribute to congenital heart disease by inhibiting cardiomyocyte proliferation.
3. WDR62 is required for centriole duplication in spermatogenesis and manchette removal in spermiogenes…
4. Modeling microcephaly with cerebral organoids reveals a WDR62-CEP170-KIF2A pathway promoting cilium …
5. Analysis of genome-wide knockout mouse database identifies candidate ciliopathy genes.

There were no clinical trials for XM_001162664