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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Lhx1
LIM homeobox protein 1
MGI:99783
13 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Cer1tm1Bhr/Cer1tm1Bhr
Lhx1tm1Bhr/Lhx1+
involves: 129S7/SvEvBrd * C57BL/6
no abnormal phenotype detected J:62080
En1tm2(cre)Wrst/En1+
Lhx1tm1Tmj/Lhx1tm2.1Bhr
Lhx5tm1Lmgd/Lhx5tm1Lmgd
involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ
absent Purkinje cell layer J:123471
decreased Purkinje cell number J:123471
small cerebellum J:123471
Lhx1tm1Bhr/Lhx1+
Pgap1oto/Pgap1+
involves: 129S7/SvEvBrd * C57BL/6J * STOCK In(1)1Rk/J
abnormal telencephalon morphology J:41878
Lhx1tm1Bhr/Lhx1+
Pgap1oto/Pgap1oto
involves: 129S7/SvEvBrd * C57BL/6J * STOCK In(1)1Rk/J
abnormal brain morphology J:41878
abnormal diencephalon morphology J:41878
abnormal telencephalon morphology J:41878
Lhx1tm1Bhr/Lhx1+
Ssbp3Tg(SOD1)1Hssk/Ssbp3+
involves: 129S7/SvEvBrd * C3H/He * C57BL/6 * ICR
embryonic growth retardation J:98485
failure of initiation of embryo turning J:98485
microcephaly J:98485
Lhx1tm1Bhr/Lhx1tm1Bhr
Pgap1oto/Pgap1+
involves: 129S7/SvEvBrd * C57BL/6J * STOCK In(1)1Rk/J
abnormal brain morphology J:41878
abnormal developmental patterning J:41878
Lhx1tm1Tmj/Lhx1+
Rettm1Kln/Rettm1Kln
Tg(Nes-cre)1Kln/0
involves: 129/Sv * BALB/c * C57BL/6 * CBA/J * SJL
abnormal axon guidance J:110955
Lhx1tm1Tmj/Lhx1+
Rettm1.1Kln/Rettm1.1Kln
involves: 129/Sv * BALB/c * C57BL/6 * CBA/J
abnormal axon guidance J:110955
Lhx1tm1Tmj/Lhx1tm4Bhr
Lhx5tm1Lmgd/Lhx5tm1Lmgd
Tg(Nes-cre)1Kln/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
absent cerebellar foliation J:123471
absent Purkinje cell layer J:123471
decreased Purkinje cell number J:123471
small cerebellum J:123471

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
08/13/2019
MGI 6.14
The Jackson Laboratory