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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cldn19
claudin 19
MGI:3033992
9 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Cldn19tm1.1(KOMP)Vlcg/Cldn19tm1.1(KOMP)Vlcg
B6N(Cg)-Cldn19tm1.1(KOMP)Vlcg/J
abnormal sleep behavior J:211773
increased circulating sodium level J:211773
increased heart weight J:211773
shortened PQ interval J:211773
shortened PR interval J:211773
shortened ST segment J:211773
Cldn19tm1Sts/Cldn19tm1Sts
involves: 129S4/SvJae * C57BL/6
abnormal gait J:99659
abnormal Schwann cell morphology J:99659
impaired coordination J:99659

Contributing Projects:
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
04/16/2024
MGI 6.23
The Jackson Laboratory