Symbol Name ID |
Celsr1
cadherin, EGF LAG seven-pass G-type receptor 1 MGI:1100883 |
Darker colors indicate more annotations |
Mouse Phenotypes | abnormal outer hair cell kinocilium location or orientation |
abnormal neural plate morphology |
abnormal neural tube closure |
delayed neural tube closure |
incomplete rostral neuropore closure |
open neural tube |
craniorachischisis |
abnormal orientation of outer hair cell stereociliary bundles |
cochlear outer hair cell degeneration |
hydrocephaly |
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Availability | Mouse Genotype | ||||||||||
Celsr1Crsh/Celsr1Crsh | |||||||||||
Celsr1ctb-2J/Celsr1ctb-2J | |||||||||||
Celsr1ctb/Celsr1ctb | |||||||||||
Celsr1Scy/Celsr1Scy | |||||||||||
Celsr1tm1.1Fati/Celsr1tm1.1Fati | |||||||||||
Celsr1Crsh/Celsr1+ | |||||||||||
Celsr1Crsh/Celsr1Scy | |||||||||||
Celsr1Scy/Celsr1+ |
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 02/16/2021 MGI 6.16 |
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