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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Celsr1
cadherin, EGF LAG seven-pass G-type receptor 1
MGI:1100883
49 phenotypes from 7 alleles in 11 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Celsr1Crsh/Celsr1+
C3H.Cg-Celsr1Crsh
delayed neural tube closure J:216413
head shaking J:216413
Celsr1Crsh/Celsr1+
involves: 101/H * BALB/c * C3H/HeH
abnormal cochlear sensory epithelium morphology J:84285
abnormal orientation of outer hair cell stereociliary bundles J:84285
head shaking J:84285, J:216413
spinning J:84285
Celsr1Crsh/Celsr1Crsh
C3H.Cg-Celsr1Crsh
abnormal neural plate morphology J:216413
craniorachischisis J:216413
open neural tube J:216413
Celsr1Crsh/Celsr1Crsh
either: (involves: 101/H * C3H/HeH) or (involves: 101/H * BALB/c * C3H/HeH)
abnormal branching involved in lung morphogenesis J:159690
abnormal lung epithelium morphology J:159690
abnormal lung lobe morphology J:159690
abnormal lung morphology J:159690
abnormal lung saccule morphology J:159690
abnormal respiratory conducting tube morphology J:159690
dilated terminal bronchiole tubes J:159690
impaired branching involved in terminal bronchiole morphogenesis J:159690
pulmonary hypoplasia J:159690
small lung J:159690
small lung lobe J:159690
thick lung-associated mesenchyme J:159690
Celsr1Crsh/Celsr1Crsh
involves: 101/H * BALB/c * C3H/HeH
abnormal cochlear sensory epithelium morphology J:84285
abnormal orientation of outer hair cell stereociliary bundles J:84285
abnormal outer hair cell kinocilium morphology J:84285
absent eyelids J:84285
craniorachischisis J:84285, J:216413
incomplete rostral neuropore closure J:84285
perinatal lethality, complete penetrance J:84285
Celsr1Crsh/Celsr1Scy
involves: 101/H * BALB/c * C3H/He * C3H/HeH
craniorachischisis J:84285
Celsr1ctb-2J/Celsr1ctb-2J
STOCK Celsr1ctb-2J/GrsrJ
abnormal coat appearance J:229303
circling J:229303
curly tail J:229303
deafness J:229303
decreased body size J:229303
head tossing J:229303
hydroencephaly J:229303
impaired hearing J:229303
increased or absent threshold for auditory brainstem response J:229303
increased susceptibility to otitis media J:229303
prenatal lethality J:229303
prenatal lethality, incomplete penetrance J:229303
reduced fertility J:229303
ruffled hair J:229303
testicular atrophy J:229303
Celsr1ctb/Celsr1ctb
CByJ.Cg-Celsr1ctb/GrsrJ
abnormal coat appearance J:229303
circling J:229303
curly tail J:229303
deafness J:229303
decreased body size J:229303
head tossing J:229303
hydroencephaly J:229303
impaired hearing J:229303
increased or absent threshold for auditory brainstem response J:229303
increased susceptibility to otitis media J:229303
prenatal lethality, incomplete penetrance J:229303
reduced fertility J:229303
ruffled hair J:229303
testicular atrophy J:229303
Celsr1Scy/Celsr1+
involves: BALB/cAnN * C3H/He * C3H/HeH
abnormal cochlear sensory epithelium morphology J:84285
abnormal organ of Corti supporting cell morphology J:84285
abnormal orientation of outer hair cell stereociliary bundles J:84285
cochlear outer hair cell degeneration J:84285
head shaking J:84285
spinning J:84285
Celsr1Scy/Celsr1+
involves: BALB/cAnNCrl * C3H/HeN
abnormal involuntary movement J:63816
head bobbing J:63816
Celsr1Scy/Celsr1Scy
involves: BALB/cAnN * C3H/He * C3H/HeH
abnormal cochlear sensory epithelium morphology J:84285
abnormal orientation of outer hair cell stereociliary bundles J:84285
abnormal outer hair cell kinocilium morphology J:84285
absent eyelids J:84285
craniorachischisis J:84285
incomplete rostral neuropore closure J:84285
perinatal lethality, complete penetrance J:84285
Celsr1tm1.1Fati/Celsr1tm1.1Fati
involves: 129S1/Sv * 129X1/SvJ
abnormal hair follicle orientation J:157059
abnormal neural tube closure J:157059
cranioschisis J:157059
kinked tail J:157059
prenatal lethality, incomplete penetrance J:157059
whorled hair J:157059
Celsr1tm1Fati/Celsr1tm1Fati
Emx1tm1(cre)Krj/Emx1+
involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ
whorled hair J:157059
Gt(ROSA)26Sortm1.1(Lyn/Celsr1/EGFP)Rodr/Gt(ROSA)26Sor+
involves: FVB/N
abnormal anterior visceral endoderm cell migration J:170681
Gt(ROSA)26Sortm1.1(Lyn/Celsr1/EGFP)Rodr/Gt(ROSA)26Sortm1.1(Lyn/Celsr1/EGFP)Rodr
involves: FVB/N
abnormal anterior visceral endoderm cell migration J:170681

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last database update
11/07/2017
MGI 6.11
The Jackson Laboratory