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RP1;jsessionid=920ECB42E64C14162267BDAB971CEAFA
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Fallopian tube
Peritoneum
Omental adipose tissue
Bladder
Placenta
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Disease Atlas
Most Correlated Diseases
Hyperlipidemia
Encephalomyelitis
Fibrosis of lung
Delayed hypersensitivity disorder
Retinal disorder
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Most Correlated Compounds
Zymosan
Dkk1 protein, mouse
Aflatoxins
C-Peptide
interleukin-34, mouse
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Most Correlated Gene Perturbations
PALB2
APPL1
RAPGEF3
PLN
OTX2
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Curated Studies
Most Correlated Studies
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Literature
Most Relevant Literature
RP1-associated recessive retinitis pigmentosa caused by paternal uniparental disomy.
Identification of a novel nonsense mutation in RP1 that causes autosomal recessive retinitis pigment…
In Silico identification of a common mobile element insertion in exon 4 of RP1.
Biallelic RP1-associated retinal dystrophies: Expanding the mutational and clinical spectrum.
A founder Alu insertion in RP1 gene in Japanese patients with retinitis pigmentosa.
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There were no clinical trials for RP1;jsessionid=920ECB42E64C14162267BDAB971CEAFA
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