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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Klhdc2
kelch domain containing 2
MGI:1916804
12 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Klhdc2tm1a(EUCOMM)Hmgu/Klhdc2+
C57BL/6N-Klhdc2tm1a(EUCOMM)Hmgu/H
corneal opacity J:165965
hypoactivity J:165965
increased body weight J:165965
tremors J:165965
Klhdc2tm1b(EUCOMM)Hmgu/Klhdc2+
C57BL/6N-Klhdc2tm1b(EUCOMM)Hmgu/H
abnormal head morphology J:211773
abnormal skin morphology J:211773
abnormal snout morphology J:211773
enlarged heart J:211773
prolonged PQ interval J:211773
prolonged PR interval J:211773
small thymus J:211773
Klhdc2tm1b(EUCOMM)Hmgu/Klhdc2tm1b(EUCOMM)Hmgu
C57BL/6N-Klhdc2tm1b(EUCOMM)Hmgu/H
preweaning lethality, complete penetrance J:211773

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
10/01/2019
MGI 6.14
The Jackson Laboratory