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XB-GENEPAGE-853647
foxj1 forkhead box J1
Expression Phenotypes
Gene expression phenotype annotations where the gene of interest has been
disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from
differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1,
FDR <= 0.05 and an absolute LogFC >= 2.
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| Manual annotations: foxj1 manipulated (7 sources), foxj1 assayed (18 sources) |
| Computed annotations: foxj1 assayed (18 sources) |
| Diseases
Diseases from the human disease ontology (DO) manually associated with phenotypes
from disease models. Sources are grouped by anatomical (AP) and expression (EP) phenotypes.
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| situs inversus (1 EP source), visceral heterotaxy (1 EP source), allergic rhinitis (), autoimmune disease () |
| Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting
the gene of interest.
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| Xla Wt + foxj1 (1 source), Xla Wt + foxj1 (1 source), Xla Wt + foxj1 (1 source), Xla Wt + foxj1 CRISPR (1 source), Xla Wt + foxj1 CRISPR (1 source), Xla Wt + foxj1 MO (1 source), Xla wt + foxj1 sgnRNA1 CRISPR (1 source), Xtr Wt + foxj1 CRISPR (1 source), Xtr Wt + foxj1 MO (1 source) |
| Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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| Human (35 sources): Abnormality of the digestive system, Abnormality of the immune system, Airway obstruction, Asplenia, Asthma, Atelectasis, Bronchiectasis, Chronic bronchitis, Chronic otitis media, Chronic sinusitis, [+] |
| Mouse (36 sources): abnormal brain development, abnormal brain ependyma morphology, abnormal brain ventricle morphology, abnormal choroid plexus morphology, abnormal embryonic cilium location or orientation, abnormal left-right axis patterning, abnormal neuron differentiation, abnormal olfactory bulb development, abnormal postnatal subventricular zone morphology, abnormal primitive node morphology, [+] |
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View all ortholog results at Monarch |