About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Lhx1
LIM homeobox protein 1
MGI:99783
80 phenotypes from 8 alleles in 11 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
En1tm2(cre)Wrst/En1+
Lhx1tm2.1Bhr/Lhx1tm2.1Bhr
involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ
no abnormal phenotype detected J:123471
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Tg(CAG-Lhx,-EGFP)1Eno/?
involves: C3H * C57BL/6
failure of intramembranous bone ossification J:150709
frontal bone foramen J:150709
intracranial hemorrhage J:150709
neonatal lethality, complete penetrance J:150709
Lhx1tm1a(EUCOMM)Wtsi/Lhx1+
C57BL/6N-Lhx1tm1a(EUCOMM)Wtsi/Ics
decreased circulating alkaline phosphatase level J:165965
Lhx1tm1Bhr/Lhx1+
involves: 129S7/SvEvBrd * C3H/He * C57BL/6 * ICR
no abnormal phenotype detected J:98485
Lhx1tm1Bhr/Lhx1tm1Bhr
involves: 129S7/SvEvBrd
abnormal primitive streak elongation J:74124
abnormal primitive streak formation J:74124
abnormal rostral-caudal axis patterning J:74124
Lhx1tm1Bhr/Lhx1tm1Bhr
involves: 129S7/SvEvBrd * C57BL/6
abnormal allantois morphology J:24115
abnormal anterior head development J:24115
abnormal brain development J:24115
abnormal egg cylinder morphology J:24115
abnormal gastrulation movements J:24115
abnormal hindbrain development J:24115
abnormal primitive node morphology J:24115
abnormal spinal cord morphology J:24115
absent forebrain J:24115
absent kidney J:24115
absent midbrain J:24115
absent ovary J:24115
absent prechordal mesoderm J:24115
absent testes J:24115
acephaly J:24115
agonadal J:24115
decreased embryo size J:24115
dilated allantois J:24115
embryonic lethality during organogenesis, incomplete penetrance J:24115
embryonic-extraembryonic boundary constriction J:24115
incomplete embryo turning J:24115
perinatal lethality, complete penetrance J:24115
rostral-caudal axis duplication J:24115
small allantois J:24115
Lhx1tm1Bhr/Lhx1tm1Tmj
involves: 129S/SvEv * C57BL/6
abnormal anterior head development J:98831
abnormal female reproductive system morphology J:98831
abnormal male reproductive system morphology J:98831
absent metanephros J:98831
absent ureter J:98831
Lhx1tm1Bhr/Lhx1tm2.1Rob
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S/SvEv * C57BL/6 * C57BL/6N * CBA
abnormal endoderm development J:226614
abnormal heart looping J:226614
abnormal heart morphology J:226614
abnormal nervous system development J:226614
abnormal primitive node morphology J:226614
cardia bifida J:226614
cellular necrosis J:226614
embryonic growth retardation J:226614
enlarged pericardium J:226614
Lhx1tm1Tmj/Lhx1tm2.1Bhr
Tg(Pax2-cre)10Shwl/0
involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6 * CD-1 * SJL
abnormal kidney morphology J:104938
abnormal ureter morphology J:104938
abnormal ureteric bud elongation J:104938
abnormal Wolffian duct morphology J:104938
duplex kidney J:104938
hydronephrosis J:104938
impaired branching involved in ureteric bud morphogenesis J:104938
neonatal lethality, complete penetrance J:104938
renal hypoplasia J:104938
rudimentary Mullerian ducts J:104938
rudimentary Wolffian ducts J:104938
single kidney J:104938
small kidney J:104938
Wolffian duct degeneration J:104938
Lhx1tm2.1Bhr/Lhx1tm1Tmj
Tg(Hoxb7-cre)13Amc/0
involves: 129S/SvEv * C57BL/6
abnormal mesonephros morphology J:98831
abnormal Mullerian duct morphology J:98831
abnormal ureter development J:98831
abnormal ureteric bud morphology J:98831
absent epididymis J:98831
absent Mullerian ducts J:98831
absent uterus J:98831
absent vas deferens J:98831
decreased nephron number J:98831
decreased renal glomerulus number J:98831
ectopic ureter J:98831
hydronephrosis J:98831
hydroureter J:98831
Mullerian duct degeneration J:98831
renal hypoplasia J:98831
rudimentary Mullerian ducts J:98831
small metanephros J:98831
uterus hypoplasia J:98831
Wolffian duct degeneration J:98831
Lhx1tm2.1Bhr/Lhx1tm1Tmj
Tg(Rarb-cre)1Bhr/0
involves: 129S/SvEv * C57BL/6 * SJL
abnormal kidney development J:98831
abnormal kidney medulla development J:98831
abnormal urinary bladder morphology J:98831
absent nephron J:98831
absent renal glomerulus J:98831
neonatal lethality, complete penetrance J:98831
renal hypoplasia J:98831
small metanephros J:98831
Lhx1tm3.1Bhr/Lhx1tm3.1Bhr
involves: 129S7/SvEvBrd * C57BL/6
abnormal anterior head development J:63192
abnormal neural tube morphology J:63192
abnormal primitive streak elongation J:63192
absent forebrain J:63192
absent midbrain J:63192
embryonic lethality during organogenesis, complete penetrance J:63192
embryonic-extraembryonic boundary constriction J:63192
Lhx1tm4Bhr/Lhx1tm4Bhr
Tg(Nes-cre)1Kln/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
neonatal lethality, complete penetrance 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory