Gene entry
CUL4B
cullin 4B
- Chromosome
- X
- Cytoband
- Xq24
- Variants (rsID)
- 7
CUL4B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xq24). Its official name is “cullin 4B”. The reference table lists 7 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs121434616Pathogenicsingle nucleotide variantX-linked intellectual disability Cabezas type|Intellectual disability|Global developmental delay|Abnormal facial shape|Seizure|Short stature
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.