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TTC25
(gene)
Summary
General Info
Body Atlas
Most Correlated Tissues
Testes
Fallopian tube
Bronchus
Trachea
Peritoneum
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Disease Atlas
Most Correlated Diseases
Immotile cilia syndrome
Cryptococcosis
Mycobacteriosis
Tuberculosis
Sepsis due to Gram negative bacteria
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Pharmaco Atlas
Most Correlated Compounds
monomethyl phthalate
salubrinal
mono-benzyl phthalate
11-ketotestosterone
fibroblast growth factor 21
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Knockdown Atlas
Most Correlated Gene Perturbations
PWWP2A
CCDC170
RPTOR
TMEFF2
SIRT6
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Curated Studies
Most Correlated Studies
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Literature
Most Relevant Literature
A splice site and copy number variant responsible for TTC25-related primary ciliary dyskinesia.
TTC25 Deficiency Results in Defects of the Outer Dynein Arm Docking Machinery and Primary Ciliary Dy…
CFAP53 regulates mammalian cilia-type motility patterns through differential localization and recrui…
Variants in TTC25 affect autistic trait in patients with autism spectrum disorder and general popula…
RFX2 is broadly required for ciliogenesis during vertebrate development.
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Clinical Trials
Most Relevant Clinical Trials
There were no clinical trials for TTC25
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