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Summary Expression Phenotypes Gene Literature (48) GO Terms (20) Nucleotides (197) Proteins (49) Interactants (714) Wiki
XB-GENEPAGE-1194371

foxh1     forkhead box H1

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.
Manual annotations: foxh1 manipulated (5 sources)
Computed annotations: foxh1 assayed (10 sources)
Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting the gene of interest.
Xla Wt + foxh1 + smad2 (1 source), Xla Wt + foxh1 mKD (1 source), Xla Wt + foxh1-EnR (1 source), Xla Wt + foxh1-VP16 (1 source), Xla Wt + foxh1-VP16-GR + DEX (1 source)
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (35 sources): Abnormality of cardiovascular system morphology, Agenesis of corpus callosum, Ambiguous genitalia, Anteverted nares, Asthma, Choanal atresia, Cleft palate, Cyclopia, Duodenal atresia, EMG: myopathic abnormalities, [+]
Mouse (43 sources): abdominal situs ambiguus, abnormal anterior head development, abnormal anterior primitive streak morphology, abnormal azygos vein morphology, abnormal cardiac outflow tract development, abnormal cranium morphology, abnormal heart development, abnormal heart looping, abnormal heart position or orientation, abnormal hepatic portal vein morphology, [+]

View all ortholog results at Monarch