FIGURE

Fig. S3

ID

ZDB-FIG-180717-11

Publication

Gao et al., 2018 - Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss.

Other Figures

Fig. 3
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Fig. 5
Fig. S2
Fig. S3
Fig. S4

All Figure Page

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Fig. S3

Expression Data

Expression Detail

Antibody Labeling

Phenotype Data

Fish:	AB + MO3-ifnlr1
Knockdown Reagent:	MO3-ifnlr1
Observed In:	whole organism apoptotic process
Stage:	Protruding-mouth

Phenotype Detail

Acknowledgments

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