Symbol Name ID |
Ednrb
endothelin receptor type B MGI:102720 |
Darker colors indicate more annotations |
Human Phenotypes | Conductive hearing impairment |
Sensorineural hearing impairment |
Hearing impairment |
Disease(s) Associated with EDNRB | |||
ABCD syndrome | |||
Hirschsprung's disease | |||
Waardenburg syndrome | |||
Waardenburg syndrome type 4A |
Mouse Phenotypes | abnormal inner ear morphology |
abnormal cochlea morphology |
abnormal cochlear sensory epithelium morphology |
abnormal cochlear hair cell morphology |
cochlear hair cell degeneration |
abnormal Deiters cell morphology |
organ of Corti degeneration |
abnormal stria vascularis morphology |
absent strial intermediate cells |
thin stria vascularis |
abnormal hearing physiology |
deafness |
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Availability | Mouse Genotype | ||||||||||||
Ednrbs-l/Ednrbs-l | |||||||||||||
EdnrbWS4/EdnrbWS4 |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/30/2024 MGI 6.23 |
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