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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Tbx22
T-box 22
MGI:2389465
17 phenotypes from 3 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Tbx22tm1.1(KOMP)Vlcg/Y
C57BL/6N-Tbx22tm1.1(KOMP)Vlcg/J
increased circulating HDL cholesterol level J:211773
Tbx22tm1.1(KOMP)Vlcg/Tbx22tm1.1(KOMP)Vlcg
C57BL/6N-Tbx22tm1.1(KOMP)Vlcg/J
increased mean corpuscular hemoglobin J:211773
Tbx22tm1.1Sta/Y
involves: 129/Sv * CD-1
abnormal bone mineralization J:153100
abnormal intramembranous bone ossification J:153100
abnormal osteoblast differentiation J:153100
abnormal palatal rugae morphology J:153100
abnormal vomer bone morphology J:153100
choanal atresia J:153100
cleft secondary palate J:153100
decreased palatine bone horizontal plate size J:153100
palate bone hypoplasia J:153100
perinatal lethality, incomplete penetrance J:153100
persistent oronasal membrane J:153100
respiratory distress J:153100
tongue ankylosis J:153100
Tbx22tm1.1Sta/Tbx22tm1.1Sta
involves: 129 * CD-1
abnormal bone mineralization J:153100
abnormal intramembranous bone ossification J:153100
abnormal osteoblast differentiation J:153100
abnormal palatal rugae morphology J:153100
abnormal vomer bone morphology J:153100
choanal atresia J:153100
cleft secondary palate J:153100
decreased palatine bone horizontal plate size J:153100
palate bone hypoplasia J:153100
perinatal lethality, incomplete penetrance J:153100
persistent oronasal membrane J:153100
respiratory distress J:153100
small vomer bone J:153100
tongue ankylosis J:153100
Tbx22tm1Sta/Y
Not Specified
no abnormal phenotype detected J:153100
Tbx22tm1Sta/Tbx22tm1Sta
Not Specified
no abnormal phenotype detected J:153100

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