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Symbol
Name
ID
Ednrb
endothelin receptor type B
MGI:102720
Phenotype annotations related to muscle
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Spastic paraparesis
Muscular hypotonia
Disease(s) Associated with EDNRB
Waardenburg syndrome type 4A

Mouse Phenotypes
muscle phenotype
decreased vasodilation
increased cardiac muscle contractility
abnormal diaphragm morphology
Availability Mouse Genotype
Ednrbs-15DttMb/Ednrbs-15DttMb
Ednrbtm1.1Yko/Ednrbtm1.1Yko
Ednrbs-1Acrg/Ednrbs-9ThW
Ednrbs-1Acrg/Ednrbs-48UThc *
Ednrbtm1.1Nrd/Ednrb+
Ednrbtm1Yko/Ednrbtm1Yko
Tg(Tek-cre)1Ywa/0  (conditional)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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last database update
11/14/2017
MGI 6.11
The Jackson Laboratory