Genetics University — Research, Education, Medical Genetics
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Gene entry

RP2

RP2 activator of ARL3 GTPase

Chromosome
X
Cytoband
Xp11.3
Variants (rsID)
2

RP2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome X (region Xp11.3). Its official name is “RP2 activator of ARL3 GTPase”. The reference table lists 2 variants (rsID) for this gene.

Clinically classified variants

2 reference-table entries with clinical significance.

  • rs104894926Pathogenicsingle nucleotide variantRetinitis pigmentosa 2
  • rs104894927Pathogenicsingle nucleotide variantRetinitis pigmentosa 2|Retinitis pigmentosa|Retinal dystrophy

Public references

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