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Date: Tue Jan 28 2025
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Gene
Gene Ontology
Disease
Allele/Variant
Model
HTP Dataset Index
Disease
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Disease Group
central nervous system disease
1
×
disease of metabolism
1
×
Genes
MSW1 (Sce)
2
×
TrpRS-m (Dme)
2
×
WARS2 (Hsa)
2
×
Wars2 (Mmu)
2
×
Wars2 (Rno)
2
×
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Associated Species
Caenorhabditis elegans
2
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Danio rerio
2
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Drosophila melanogaster
2
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Homo sapiens
2
×
Mus musculus
2
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Rattus norvegicus
2
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Saccharomyces cerevisiae
2
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Xenopus laevis
2
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Xenopus tropicalis
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results
Page 1 of 1
Disease
Genes: prx-10 (Cel)
mitochondrial metabolism disease
Disease
Source:
DOID:700
Definition:
An inherited metabolic disorder that involves mitochondrial metabolism dysfunction.
Genes:
prx-10 (Cel)
Gene (1924)
Allele/Variant (146)
Model (44)
movement disease
Disease
Source:
DOID:480
Definition:
A brain disease that is characterized by a clinical syndrome of either hyperkinetic movement or hyperkinetic movement unrelated to weakness or spasticity.
Genes:
prx-10 (Cel)
Gene (1162)
Allele/Variant (51)
Model (30)
Page 1 of 1
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