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Date: Tue Jan 28 2025
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Gene
Gene Ontology
Disease
Allele/Variant
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HTP Dataset Index
Disease
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Disease Group
monogenic disease
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sensory system disease
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Genes
ARL3 (Hsa)
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Arl3 (Mmu)
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Arl3 (Rno)
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RP2 (Hsa)
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Rp2 (Mmu)
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Associated Species
Caenorhabditis elegans
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Danio rerio
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Drosophila melanogaster
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Homo sapiens
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Mus musculus
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Rattus norvegicus
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Disease
Models: Rp2<Gt(EUCJ0183f04)Hmgu>/Rp2<Gt(EUCJ0183f04)Hmgu> [background:] involves: C57BL/6 * C57BL/6N (Mmu)
retinitis pigmentosa 2
Disease
Source:
DOID:0110415
Definition:
A retinitis pigmentosa that has_material_basis_in mutation in the RP2 gene on chromosome Xp11.3.
Gene (17)
Allele/Variant (4)
Model (6)
Page 1 of 1
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