Cart
Humanized Models Immune-Related Mice Toolbox of Mice Genetically Edited Rats Supporting services Cell lines Other Products
Tumor Targets
Immune Checkpoints
Complements
Cytokines
Cytokine Receptors
Metabolic Targets
Viral Infection Receptors
Other Targets
Immunodeficient
Humanized Drug Targets
Cytokine Reporters
Inducible Cell Ablation
Cell-specific Reporter
Fluorescent & Other Reporters
Reporters
Find Cre
Tet-regulated
CRISPR/Cas knockins
Reporters
Cre-drivers
Immunodeficient
Humanized Drug Targets
Diseases
Model breeding
Breed conservation service
Reporter-labeled
Primary cell lines
Wild-Type
Humanized Drug Targets
Others
Manual Nucleic acid extraction kits
Automated Nucleic Acid Purification Solution
Protein Affinity Resins
Antibody Affinity Resins
Home / Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss.

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

Gene Summary

Gene Name

Model Description

-
Order Form

Please fill in the order form and we will contact you within 2 working days.

  • h4-1BB(2) NM-HU-190077 1

    Email Back to top