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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Pou2f1
POU domain, class 2, transcription factor 1
MGI:101898
16 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Pou2f1tm1Cav/Pou2f1tm1Cav
involves: 129P2/OlaHsd * C57BL/6
abnormal anterior visceral endoderm morphology J:165572
abnormal embryo development J:165572
abnormal embryonic-extraembryonic boundary morphology J:165572
abnormal extraembryonic ectoderm morphology J:165572
absent ectoplacental cone J:165572
decreased embryo size J:165572
embryonic growth arrest J:165572
embryonic lethality between implantation and placentation, complete penetrance J:165572
Pou2f1tm1Shrp/Pou2f1tm1Shrp
involves: 129S4/SvJae * C57BL/6
abnormal erythropoiesis J:87664
anemia J:87664
decreased embryo size J:87664
embryonic lethality during organogenesis, incomplete penetrance J:87664
lethality throughout fetal growth and development, complete penetrance J:87664
pallor J:87664
small lens J:119175
small liver J:87664
normal vision/eye phenotype 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
06/18/2019
MGI 6.14
The Jackson Laboratory