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