Symbol Name ID |
Ednrb
endothelin receptor type B MGI:102720 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Aganglionic megacolon |
Total intestinal aganglionosis |
Spastic paraparesis |
Leukodystrophy |
Myelomeningocele |
Ataxia |
Abnormal auditory evoked potentials |
Intellectual disability |
Global developmental delay |
Polyneuropathy |
Disease(s) Associated with EDNRB | ||||||||||
ABCD syndrome | ||||||||||
Hirschsprung's disease | ||||||||||
Waardenburg syndrome | ||||||||||
Waardenburg syndrome type 4A |
Mouse Phenotypes | nervous system phenotype |
abnormal cochlear hair cell morphology |
cochlear hair cell degeneration |
abnormal nervous system morphology |
abnormal enteric nervous system morphology |
abnormal enteric neuron morphology |
absent enteric neurons |
abnormal brain morphology |
abnormal neuromuscular synapse morphology |
abnormal phrenic nerve morphology |
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Availability | Mouse Genotype | ||||||||||
Ednrbs-15DttMb/Ednrbs-15DttMb | |||||||||||
Ednrbs-36Pub/Ednrbs-36Pub | |||||||||||
Ednrbs-l/Ednrbs-l | |||||||||||
EdnrbWS4/EdnrbWS4 | |||||||||||
Ednrbs-1Acrg/Ednrbs-9ThW | |||||||||||
Ednrbs-1Acrg/Ednrbs-48UThc | * | ||||||||||
Ednrbtm1(tTA)Tilg/Ednrbtm3(tetO)Tilg | |||||||||||
Ednrbtm2(rtTA)Tilg/Ednrbtm3(tetO)Tilg |
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 08/02/2024 MGI 6.24 |
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