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Gene entry

CUL3

cullin 3

Chromosome
2
Cytoband
2q36.2
Variants (rsID)
16

CUL3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2q36.2). Its official name is “cullin 3”. The reference table lists 16 variants (rsID) for this gene.

Clinically classified variants

2 reference-table entries with clinical significance.

  • rs2396092Benignsingle nucleotide variantAutosomal dominant pseudohypoaldosteronism type 1|Pseudohypoaldosteronism type 2E
  • rs3738952Benignsingle nucleotide variantAutosomal dominant pseudohypoaldosteronism type 1|Pseudohypoaldosteronism type 2E

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.