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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
11 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Celsr1Crsh/Celsr1+
Vangl2Lp/Vangl2+
C3H.Cg-Vangl2Lp Celsr1Crsh
abnormal eyelid morphology J:216413
abnormal left-right axis patterning J:216413
craniorachischisis J:216413
omphalocele J:216413
Celsr1Crsh/Celsr1+
Vangl2Lp/Vangl2+
involves: 101/H * BALB/c * C3H/HeH * CBA * LPT/Le
craniorachischisis J:216413
curly tail J:216413
Celsr1Crsh/Celsr1+
ScribCrc/Scrib+
C3H.Cg-ScribCrc Celsr1Crsh
abnormal abdominal wall morphology J:216413
abnormal developmental patterning J:216413
abnormal eyelid development J:216413
abnormal eyelid morphology J:216413
craniorachischisis J:216413
curly tail J:216413
exencephaly J:216413
spina bifida J:216413
Celsr1Crsh/Celsr1+
ScribCrc/Scrib+
involves: 101/H * BALB/c * C3H/HeH * C57BL/6 * NMRI
craniorachischisis J:216413
Celsr1Crsh/Celsr1+
ScribCrc/Scrib+
Vangl2Lp/Vangl2+
C3H.Cg-Vangl2Lp ScribCrc Celsr1Crsh
abnormal tail morphology J:216413
craniorachischisis J:216413
exencephaly J:216413
Celsr1Crsh/Celsr1+
Ptk7chz/Ptk7+
involves: 101/H * BALB/c * BALB/cAnN * C3H/HeH
spina bifida J:163834
Celsr1Scy/Celsr1+
ScribCrc/Scrib+
C3H.Cg-ScribCrc Celsr1Scy
abnormal abdominal wall morphology J:216413
abnormal eyelid morphology J:216413
craniorachischisis J:216413

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