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FAM161A
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Summary
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Body Atlas
Most Correlated Tissues
Testes
Fetal brain
Caudate
Pituitary gland
Ovary
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Disease Atlas
Most Correlated Diseases
Hereditary white blood cell disorder
Disorder of neutrophils
Gastrointestinal hemorrhage
Helicobacter pylori gastrointestinal tract infection
Primary immune deficiency disorder
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Most Correlated Compounds
Nitric Oxide
Ions
Enterotoxins
EMD 121974
N-(1-naphthyl)ethylenediamine
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Most Correlated Gene Perturbations
MIR27A
PCSK9
SFRP1
OTX2
G9a
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Curated Studies
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Literature
Most Relevant Literature
A new mouse model for retinal degeneration due to Fam161a deficiency.
The connecting cilium inner scaffold provides a structural foundation that protects against retinal …
Fine-tuning FAM161A gene augmentation therapy to restore retinal function.
Disruption of the retinitis pigmentosa 28 gene Fam161a in mice affects photoreceptor ciliary structu…
Gene augmentation therapy attenuates retinal degeneration in a knockout mouse model of Fam161a retin…
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Clinical Trials
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