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The dHb Phenotype of tcf7l2 Mutants Is Epistatic to the Effects of a Mutation in axin1 that Enhances Wnt Signaling
Dorsal views of the habenulae of 4 dpf embryos of genotype shown to the left labeled with markers shown above columns (A–D′). The enhanced expression of kctd12.1 and reduced expression of kctd8 in tcf7l2 mutants is observed irrespective of the presence (C and C′) or absence (D and D′) of functional Axin1. See also Table S3.
