Comparative

OMIA group 2163

Cone dystrophy 4, PDE6C-related

The chain reaches the human disease cone dystrophy 4, which Mondo defines as: “Any cone dystrophy in which the cause of the disease is a mutation in the PDE6C gene.”

The chain

From the animal disease to the drugs. The page shows what each step found and where the chain stopped. It does not say whether the animal is a model of a human disease.

  1. Animal disease

    Reached

    OMIA records it in 1 species entry marked as a defect.

  2. Human disease

    Reached

    1 Mondo disease.

  3. Human gene

    Reached

    1 human gene.

  4. Target evidence

    Stopped here

    None of the group's human diseases is in Open Targets.

  5. Drugs

    Not reached

    The chain stopped before this step.

The chain stopped at Target evidence: None of the group's human diseases is in Open Targets.

Natural-model score

How complete and how well supported the chain to each human disease is, out of 100, by stated rules. It does not say that the animal is a validated model of the human disease. How the score works.

cone dystrophy 4

34.0 out of 100

Part Computed from Points
Target evidence No Open Targets association with this disease 0.0 of 35
Drugs No drug has been tested for this disease, and none acts on its genes 0.0 of 25
Ortholog One to one ortholog 20.0 of 20
Both routes Both routes found this disease 10.0 of 10
Species 1 naturally occurring species entry marked as a defect 4.0 of 10

Species

The chain follows only the species entries that OMIA marks as a defect.

Species Scientific name OMIA entry A defect
Rhesus monkey Macaca mulatta OMIA:002163-9544 Yes

Genes

Each gene OMIA records for a species entry, and the human gene it reaches through Ensembl's orthologs.

Species Animal gene Human gene Ortholog
Rhesus monkey PDE6C phosphodiesterase 6C NCBI Gene 700261 PDE6C Ensembl one to one

Human diseases

Two routes lead from an OMIA group to a Mondo human disease: OMIA's own Mondo link, and the group's OMIM numbers through Mondo's cross-references.

Mondo disease Name Found by
MONDO:0013129 cone dystrophy 4 Any cone dystrophy in which the cause of the disease is a mutation in the PDE6C gene. Both routes

Target evidence

Each Open Targets association between one of the group's human genes and one of its human diseases, with its overall score and the score for each kind of evidence.

The chain did not reach target evidence.

Drugs

The chain did not reach the drugs.