FIGURE

Fig. S3

ID

ZDB-FIG-160517-28

Publication

Hsu et al., 2015 - A new mib allele with a chromosomal deletion covering foxc1a exhibits anterior somite specification defect.

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Fig. S3

The maternal effect on phenotypes of transheterozygotes (mib^ta52b/mibⁿⁿ²⁰⁰²) at 34 hpf. The transheterozygotes have typical mib phenotype at 34 hpf, including less pigmentation and curly tail. Note that the transheterozygous embryos from incrosses of male mibⁿⁿ²⁰⁰² carrier and female mib^ta52b carrier (left) showed a more severe pigmentation phenotype (typical white tail phenotype of ta52b allele¹⁷) than those from incrosses of male mib^ta52b carrier and female mibⁿⁿ²⁰⁰² carrier (right).

Expression Data

Expression Detail

Antibody Labeling

Phenotype Data

Fish:	mib1^ta52b/+; Df(Chr2:mib1,foxc1a,rab18b,yme1l1b,gata6,cables1,foxc1a,cldn1,znfl2a,dvl3a,selenot1a))nn2002/+ mib1^ta52b/+; Df(Chr2:mib1,foxc1a,rab18b,yme1l1b,gata6,cables1,foxc1a,cldn1,znfl2a,dvl3a,selenot1a))nn2002/+
Observed In:	caudal fin pigment cell
Stage:	Prim-15

Phenotype Detail

Acknowledgments

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