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XB-GENEPAGE-960147
wnt2b Wnt family member 2B
Anatomical Phenotypes
Phenotypes manually curated with terms from the Xenopus phenotype ontology
covering anatomical, gene ontology, and neurobehavioral phenotypes.
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absent lung bud (1 source) |
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: wnt2b manipulated (2 sources), wnt2b assayed (13 sources) |
Computed annotations: wnt2b assayed (3 sources) |
Experiments (Reagents)
These are short form descriptions of experiments using reagents targeting
the gene of interest.
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Xtr Wt + wnt2b MO (2 sources) |
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (4 sources): Diarrhea, Failure to thrive, Ischemic stroke, Villous atrophy |
Mouse (5 sources): abnormal kidney morphology, irregularly shaped pupil, no abnormal phenotype detected, persistence of hyaloid vascular system, small spleen |
View all ortholog results at Monarch |