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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Clec3b
C-type lectin domain family 3, member b
MGI:104540
9 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Clec3btm1b(KOMP)Wtsi/Clec3btm1b(KOMP)Wtsi
B6N(Cg)-Clec3btm1b(KOMP)Wtsi/3J
decreased grip strength J:211773
Clec3btm1Umw/Clec3btm1Umw
involves: 129S1/Sv * C57BL/6J
abnormal epiphyseal plate morphology J:72638
abnormal intervertebral disk development J:72638
abnormal intervertebral disk morphology J:72638
abnormal vertebrae morphology J:72638
abnormal vertebral body development J:72638
kyphosis J:72638
lordokyphosis J:72638
normal skeleton phenotype J:72638

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