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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Lef1
lymphoid enhancer binding factor 1
MGI:96770
54 phenotypes from 5 alleles in 7 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Lef1tm1.1(KOMP)Vlcg/Lef1+
C57BL/6N-Lef1tm1.1(KOMP)Vlcg/Ucd
abnormal heart morphology J:211773
decreased prepulse inhibition J:211773
enlarged heart J:211773
increased monocyte cell number J:211773
Lef1tm1.1(KOMP)Vlcg/Lef1tm1.1(KOMP)Vlcg
C57BL/6N-Lef1tm1.1(KOMP)Vlcg/MbpMmucd
abnormal craniofacial morphology J:211773
Lef1tm1.1(KOMP)Vlcg/Lef1tm1.1(KOMP)Vlcg
C57BL/6N-Lef1tm1.1(KOMP)Vlcg/Ucd
preweaning lethality, complete penetrance J:211773
Lef1tm1Rug/Lef1tm1Rug
involves: 129S2/SvPas
abnormal hippocampus region morphology J:59284
absent dentate gyrus J:59284
Lef1tm1Rug/Lef1tm1Rug
involves: 129S2/SvPas * C57BL/6
abnormal hair follicle development J:18378
abnormal hair follicle morphology J:18378
abnormal mammary gland bud morphology J:18378
abnormal retina vasculature morphology J:144980
abnormal vascular regression J:144980
absent alveolar process J:18378
absent barrels in primary somatosensory cortex J:18378
absent hair follicle melanin granules J:18378
absent incisors J:18378
absent lower incisors J:18378
absent mammary gland J:18378
absent mesencephalic trigeminal nucleus J:18378
absent molars J:18378
absent subcutaneous adipose tissue J:18378
absent teeth J:18378
absent upper incisors J:18378
absent vibrissae J:18378
alopecia J:18378
arrest of tooth development J:18378
decreased body size J:18378
decreased hair follicle number J:18378
normal immune system phenotype J:18378
persistence of hyaloid vascular system J:101493
pointed snout J:18378
postnatal lethality, complete penetrance J:18378
thin skin J:18378
underdeveloped hair follicles J:18378
Lef1tm1Rug/Lef1tm1Rug
involves: C57BL/6 * ICR
abnormal endometrial gland development J:189507
absent endometrial glands J:189507
Lef1tm2Rug/Lef1tm2Rug
involves: 129S2/SvPas
abnormal brain morphology J:59284
abnormal hippocampus development J:59284
absent dentate gyrus J:59284
absent hippocampus J:59284
Tg(Krt14-dnLef1)LFmw/?
involves: C57BL/6 * CBA
abnormal hair follicle orientation J:73649
abnormal skin condition J:73649
alopecia J:73649
epithelioid cyst J:73649
increased skin tumor incidence J:73649
sparse vibrissae J:73649
thick skin J:73649
Tg(Myh6-Lef1)2Tfo/Y
involves: C57BL/6J * FVB/N
perinatal lethality, complete penetrance J:109612
Tg(Myh6-Lef1)2Tfo/0
involves: C57BL/6J * FVB/N
abnormal myocardial fiber physiology J:109612
decreased heart left ventricle posterior wall thickness J:109612
decreased heart ventricle muscle contractility J:109612
dilated cardiomyopathy J:109612
dilated heart left ventricle J:109612
dilated heart right ventricle J:109612
increased heart rate J:109612

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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
09/17/2024
MGI 6.24
The Jackson Laboratory