Alternate gene names: Cullin 3, PHA2E, KIAA0617
Associated syndromes or conditions: Pseudohypoaldosteronism type II
Genomic location: 2q36.2

Diagnoses observed in people with changes in the CUL3 gene:

  • Autism Spectrum Disorder – Yes
  • Intellectual Disability or Developmental Delay - No
  • Epilepsy or Seizures - No
  • Attention Deficit Hyperactivity Disorder – No
  • Schizophrenia – No
  • Bipolar Disorder - No

Support Resources:


Infographic:


 Research Article Summaries: As we learn more from children who have these gene changes, we expect this list of resources and information to grow.

  • This gene plays an important role in cell division.


You can visit SFARI's website to see information written for researchers about this gene. SFARIgene: CUL3

Back to: Genetic Changes We're Studying