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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Pou2f1
POU domain, class 2, transcription factor 1
MGI:101898
12 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Pou2f1tm1Shrp/Pou2f1+
Pou2f2tm1Bal/Pou2f2+
involves: 129S2/SvPas * 129S4/SvJae * C57BL/6
decreased body weight J:87664
lethargy J:87664
neonatal lethality, incomplete penetrance J:87664
postnatal lethality, incomplete penetrance J:87664
Pou2f1tm1Shrp/Pou2f1+
Sox2tm1.1Vep/Sox2+
involves: 129S4/SvJae * C3H/HeN * C57BL/6
abnormal lens morphology J:119175
Pou2f1tm1Shrp/Pou2f1tm1Shrp
Sox2tm1.1Vep/Sox2+
involves: 129S4/SvJae * C3H/HeN * C57BL/6
abnormal adenohypophysis morphology J:119175
abnormal eye development J:119175
abnormal lens induction J:119175
abnormal lens morphology J:119175
abnormal pituitary diverticulum morphology J:119175
absent nasal placodes J:119175
anophthalmia J:119175
microphthalmia J:119175

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
06/11/2019
MGI 6.14
The Jackson Laboratory