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Summary
Splice variantsTranscript comparisonGene allelesSequenceSecondary StructureComparative GenomicsOntologiesPhenotypesGenetic VariationGene expressionPathwayMolecular interactionsRegulationExternal referencesSupporting evidenceID History.
nuclear receptor subfamily 0, group B, member 2 [Source:HGNC Symbol;Acc:7961]
SHP, SHP1
Chromosome 1: 27,237,980-27,240,457 reverse strand.
GRCh37:CM000663.1
This gene has 1 transcript (splice variant), 1 paralogue and is associated with 1 phenotype.
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Go to Region in Detail for more tracks and navigation options (e.g. zooming)
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