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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Satb2
special AT-rich sequence binding protein 2
MGI:2679336
54 phenotypes from 5 alleles in 5 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Satb2em3(IMPC)Tcp/Satb2+
C57BL/6NCrl-Satb2em3(IMPC)Tcp/Tcp
abnormal retina morphology J:211773
increased circulating alkaline phosphatase level J:211773
increased mean corpuscular volume J:211773
Satb2em3(IMPC)Tcp/Satb2em3(IMPC)Tcp
C57BL/6NCrl-Satb2em3(IMPC)Tcp/Tcp
abnormal craniofacial morphology J:211773
preweaning lethality, complete penetrance J:211773
Satb2Mhdabap002/Satb2Mhdabap002
C3HeB/FeJ-Satb2Mhdabap002
abnormal jaw morphology J:183993
abnormal trabecular bone morphology J:183993
brittle teeth J:183993
decreased bone mineral density J:183993
increased circulating alkaline phosphatase level J:183993
increased circulating calcium level J:183993
Satb2tm1(cre)Vit/Satb2+
involves: C57BL/6
abnormal incisor morphology J:116770
abnormal jaw morphology J:116770
abnormal nasal capsule morphology J:116770
asymmetric snout J:116770
cleft palate J:116770
decreased mouth size J:116770
microcephaly J:116770
premaxilla hypoplasia J:116770
preweaning lethality, incomplete penetrance J:116770
short snout J:116770
Satb2tm1(cre)Vit/Satb2tm1(cre)Vit
involves: C57BL/6
abnormal hyoid bone morphology J:116770
abnormal jaw morphology J:116770
abnormal molar morphology J:116770
abnormal nasal capsule morphology J:116770
absent incisors J:116770
absent submandibular gland J:116770
cleft palate J:116770
decreased tongue size J:116770
microcephaly J:116770
micrognathia J:116770
perinatal lethality J:116770
premaxilla hypoplasia J:116770
short limbs J:116770
Satb2tm1b(KOMP)Wtsi/Satb2+
C57BL/6N-Satb2tm1b(KOMP)Wtsi/Ucd
abnormal uterus morphology J:211773
enlarged lymph nodes J:211773
Satb2tm1b(KOMP)Wtsi/Satb2tm1b(KOMP)Wtsi
C57BL/6N-Satb2tm1b(KOMP)Wtsi/Ucd
preweaning lethality, complete penetrance J:211773
Satb2tm1Rug/Satb2tm1Rug
Not Specified
abnormal bone mineralization J:115876
abnormal bone ossification J:115876
abnormal bone structure J:115876
abnormal cranium morphology J:115876
abnormal first pharyngeal arch morphology J:115876
abnormal frontal bone morphology J:115876
abnormal hyoid bone body morphology J:115876
abnormal hyoid bone lesser horn morphology J:115876
abnormal hyoid bone morphology J:115876
abnormal mandible morphology J:115876
abnormal maxilla morphology J:115876
abnormal nasal bone morphology J:115876
abnormal palate morphology J:115876
abnormal premaxilla morphology J:115876
abnormal temporal bone morphology J:115876
abnormal trabecular bone morphology J:115876
absent lower incisors J:115876
absent thyroid cartilage J:115876
cleft secondary palate J:115876
cleft upper lip J:115876
decreased tongue size J:115876
impaired osteoblast differentiation J:115876
micrognathia J:115876
palatal shelves fail to meet at midline J:115876
perinatal lethality, complete penetrance J:115876
short hindlimb J:115876
short mandible J:115876
short maxilla J:115876
short tongue J:115876

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
04/09/2024
MGI 6.23
The Jackson Laboratory