Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

RDH11

retinol dehydrogenase 11

Chromosome
14
Cytoband
14q24.1
Variants (rsID)
5

RDH11 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 14 (region 14q24.1). Its official name is “retinol dehydrogenase 11”. The reference table lists 5 variants (rsID) for this gene.

Clinically classified variants

2 reference-table entries with clinical significance.

  • rs606231423Pathogenicsingle nucleotide variantRetinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome
  • rs606231424Pathogenicsingle nucleotide variantRetinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome

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.