Disease: Retinitis Pigmentosa 37

Name Retinitis Pigmentosa 37

Synonyms -

Classification eye, genetic

Phenotypes Autosomal dominant inheritance; Autosomal recessive inheritance; Cataract; Cystoid macular degeneration; Nyctalopia; Photophobia; Pigmentary retinopathy; Red-green dyschromatopsia; Rod-cone dystrophy; Tritanomaly; Undetectable light- and dark-adapted electroretinogram

Associated Genes NR2E3 (Withdrawn symbols: PNR, RP37, rd7 )

Mouse Orthologs Nr2e3 (Withdrawn symbols: A930035N01Rik, rd7 )

Source OMIM:611131 (names, synonyms, disease associated genes),
Orphanet (disease classes),
HGNC, Ensembl, MGI (gene symbols, gene orthology)
HPO (phenotypes)

Mouse Model: phenotype-based associations

Disease phenotypes are compared with mouse phenotypes, with each mouse model contributing one point to the diagram. Scores are computed according to phenotype specificity and cross-species similarity. X-axis shows the score of the single phenotype that contributes most. Y-axis shows an average among all phenotype matches. The curved line designates a visualization threshold; models below threshold are omitted, except when their genotype matches a disease-associated gene.

Mouse Models

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