Disease Annotation

Gene Info

  • Species:Human (Homo sapiens)
  • GeneID:778
  • Symbol:CACNA1F
  • Description:calcium voltage-gated channel subunit alpha1 F

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Disease_Term Source Rank Other Values
Night blindness, congenital stationary (incomplete), 2A, X-linked, 300071 (3) OMIM high
  • Genome region :Xp11.23
  • OMIM_ID :300071OMIM phenotype ID
  • OMIM_ID :300110OMIM gene ID
Aland Island eye disease, 300600 (3) OMIM high
  • Genome region :Xp11.23
  • OMIM_ID :300110OMIM gene ID
  • OMIM_ID :300600OMIM phenotype ID
Cone-rod dystrophy, X-linked, 3, 300476 (3) OMIM high
  • Genome region :Xp11.23
  • OMIM_ID :300110OMIM gene ID
  • OMIM_ID :300476OMIM phenotype ID