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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Lhx8
LIM homeobox protein 8
MGI:1096343
37 phenotypes from 4 alleles in 6 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Lhx8tm1Awan/Lhx8tm1Awan
involves: 129S2/SvPas * C57BL/6J
abnormal cholinergic neuron morphology J:100340
cleft palate J:100340
neonatal lethality, incomplete penetrance J:100340
Lhx8tm1Lmgd/Lhx8tm1Lmgd
involves: 129 * C57BL/6
abnormal double-strand DNA break repair J:262653
abnormal mitophagy J:262653
decreased oocyte number J:262653
enhanced autophagy J:262653
increased ovary apoptosis J:262653
oocyte degeneration J:262653
ovary fibrosis J:262653
postnatal lethality, incomplete penetrance J:262653
premature ovarian failure J:262653
Lhx8tm1Lmgd/Lhx8tm1Lmgd
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6
abnormal uterine horn morphology J:140898
absent oocytes J:140898
absent ovarian follicles J:140898
absent primordial ovarian follicles J:140898
decreased oocyte number J:140898
decreased primordial ovarian follicle number J:140898
female infertility J:140898
impaired ovarian folliculogenesis J:140898
oocyte degeneration J:140898
ovary atrophy J:140898
normal reproductive system phenotype J:140898
Lhx8tm1Lmgd/Lhx8tm1Lmgd
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal cholinergic neuron morphology J:84641
abnormal oogenesis J:294629
abnormal telencephalon development J:84641
cleft secondary palate J:59082
normal craniofacial phenotype J:59082
neonatal lethality, incomplete penetrance J:59082
palatal shelves fail to meet at midline J:59082
premature death J:59082
Lhx8tm1Vpa/Lhx8tm1Vpa
B6.Cg-Lhx8tm1Vpa
abnormal cholinergic neuron morphology J:101205
abnormal contextual conditioning behavior J:101205
abnormal dorsal striatum morphology J:101205
abnormal spatial learning J:101205
cleft palate J:101205
decreased body weight J:101205
preweaning lethality, incomplete penetrance J:101205
Lhx8tm1Vpa/Lhx8tm2.1Vpa
Tg(Chat-cre)GM24Gsat/0
involves: 129P2/OlaHsd * 129S4/SvJae * FVB/N
abnormal brain interneuron morphology J:182013
abnormal cholinergic neuron morphology J:182013
abnormal GABAergic neuron morphology J:182013
abnormal neuron differentiation J:182013
abnormal neuron morphology J:182013
abnormal striatum morphology J:182013
Lhx8tm1Vpa/Lhx8tm2.1Vpa
Tmem163Tg(ACTB-cre)2Mrt/0
involves: 129P2/OlaHsd * 129S4/SvJae * FVB/N
abnormal brain interneuron morphology J:182013
abnormal striatum morphology J:182013

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
08/27/2024
MGI 6.24
The Jackson Laboratory