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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Pou3f1
POU domain, class 3, transcription factor 1
MGI:101896
15 phenotypes from 4 alleles in 6 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Pou3f1tm1(Pou3f3)1Weg/Pou3f1tm1(Pou3f3)1Weg
involves: 129S1/Sv * 129X1/SvJ
no abnormal phenotype detected J:96824
Pou3f1tm1Mejr/Pou3f1tm1Mejr
involves: 129P2/OlaHsd * C57BL/6
abnormal myelination J:34465
abnormal sciatic nerve morphology J:34465
decreased body size J:34465
neonatal lethality, incomplete penetrance J:34465
tremors J:34465
Pou3f1tm1Mejr/Pou3f1tm2.1Mejr
involves: 129P2/OlaHsd
abnormal myelination J:83739
abnormal Schwann cell morphology J:83739
Pou3f1tm1Rsd/Pou3f1tm1Rsd
either: (involves: 129S4/SvJae * 129/Sv * C57BL/6J) or (involves: 129S4/SvJae * C57BL/6 * C57BL/6J)
abnormal myelination J:34460
abnormal olfactory tract morphology J:34460
abnormal phrenic nerve morphology J:34460
abnormal sciatic nerve morphology J:34460
cyanosis J:34460
normal integument phenotype J:34460
neonatal lethality, incomplete penetrance J:34460
postnatal lethality, complete penetrance J:34460
respiratory failure J:34460
Pou3f1tm1Rsd/Pou3f1tm1Rsd
involves: 129/Sv * 129S4/SvJae * C57BL/6J
postnatal lethality, complete penetrance J:34460
Pou3f1tm2.1Mejr/Pou3f1tm2.1Mejr
involves: 129P2/OlaHsd * FVB
abnormal myelination J:78939
normal mortality/aging J:78939
normal respiratory system phenotype J:78939

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
12/10/2024
MGI 6.24
The Jackson Laboratory