Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:6010
  • Symbol:RHO
  • Description:rhodopsin

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Disease_Term Source Rank Other Values
Night blindness, congenital stationary, autosomal dominant 1, 610445 (3) OMIM high
  • Genome region :3q22.1
  • OMIM_ID :180380OMIM gene ID
  • OMIM_ID :610445OMIM phenotype ID
Retinitis pigmentosa 4, autosomal dominant or recessive, 613731 (3) OMIM high
  • Genome region :3q22.1
  • OMIM_ID :180380OMIM gene ID
  • OMIM_ID :613731OMIM phenotype ID
Retinitis punctata albescens, 136880 (3) OMIM high
  • Genome region :15q26.1
  • Genome region :3q22.1
  • Genome region :6p21.1
  • OMIM_ID :136880OMIM phenotype ID
  • OMIM_ID :179605OMIM gene ID
  • OMIM_ID :180090OMIM gene ID
  • OMIM_ID :180380OMIM gene ID
Diisocyanate-induced asthma GWAS high