Gene entry
ARL13B
ARF like GTPase 13B
- Chromosome
- 3
- Cytoband
- 3q11.1-q11.2
- Variants (rsID)
- 12
ARL13B is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q11.1-q11.2). Its official name is “ARF like GTPase 13B”. The reference table lists 12 variants (rsID) for this gene.
Clinically classified variants
4 reference-table entries with clinical significance.
- rs11554412Benignsingle nucleotide variantJoubert syndrome 1|Joubert syndrome 8
- rs11718593Likely benignsingle nucleotide variant
- rs121912607Pathogenicsingle nucleotide variantJoubert syndrome 8
- rs121912608Pathogenicsingle nucleotide variantJoubert syndrome 8
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.