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Summary
Splice variantsTranscript comparisonGene allelesSequenceSecondary StructureComparative GenomicsOntologiesGO: Molecular functionGO: Biological processGO: Cellular componentPhenotypesGenetic VariationGene expressionPathwayMolecular interactionsRegulationExternal referencesSupporting evidenceID History.
peripherin 2 (retinal degeneration, slow) [Source:HGNC Symbol;Acc:9942]
AOFMD, AVMD, CACD2, DS, PRPH, RDS, RP7, TSPAN22, rd2
Chromosome 6: 42,664,340-42,690,312 reverse strand.
GRCh37:CM000668.1
This gene has 1 transcript (splice variant), 1 paralogue and is associated with 18 phenotypes.
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Go to Region in Detail for more tracks and navigation options (e.g. zooming)
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