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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rorbtm1.1(cre)Hze
targeted mutation 1.1, Hongkui Zeng
MGI:5507855
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Rorbtm1.1(cre)Hze/Rorb+ involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCr MGI:5508524
ht2
Rorbtm1.1(cre)Hze/Rorbhstp involves: 129S6/SvEvTac * C57BL/6J MGI:7505589
cn3
Gpr158tm1.1Jdw/Gpr158tm1.1Jdw
Rorbtm1.1(cre)Hze/Rorb+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * C57BL/6NCrl MGI:8324945
cn4
Plcxd2tm1.1Jdw/Plcxd2tm1.1Jdw
Rorbtm1.1(cre)Hze/Rorb+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * C57BL/6NCrl MGI:8324948


Genotype
MGI:5508524
ht1
Allelic
Composition
Rorbtm1.1(cre)Hze/Rorb+
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCr
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rorbtm1.1(cre)Hze mutation (1 available); any Rorb mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• mice are viable and fertile with no gross physical or behavioral abnormalities




Genotype
MGI:7505589
ht2
Allelic
Composition
Rorbtm1.1(cre)Hze/Rorbhstp
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rorbhstp mutation (1 available); any Rorb mutation (38 available)
Rorbtm1.1(cre)Hze mutation (1 available); any Rorb mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• compound heterozygotes pull each rear leg up to the body as they step




Genotype
MGI:8324945
cn3
Allelic
Composition
Gpr158tm1.1Jdw/Gpr158tm1.1Jdw
Rorbtm1.1(cre)Hze/Rorb+
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * C57BL/6NCrl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gpr158tm1.1Jdw mutation (0 available); any Gpr158 mutation (77 available)
Rorbtm1.1(cre)Hze mutation (1 available); any Rorb mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• dendritic spines of neurons are shifted toward a less mature phenotype, with a decrease in the fraction of mature mushroom-type spines and a concomitant increase in immature filopodia-type protrusions indicating attenuation of dendritic spin maturation
• however, dendritic spine density is unaffected
• acute cortical sections from P15-21 mice show a strong reduction in the frequency of miniature excitatory post-synaptic currents (mEPSCs)
• however, amplitude and decay time of mEPSCs are not affected




Genotype
MGI:8324948
cn4
Allelic
Composition
Plcxd2tm1.1Jdw/Plcxd2tm1.1Jdw
Rorbtm1.1(cre)Hze/Rorb+
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * C57BL/6NCrl
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Plcxd2tm1.1Jdw mutation (0 available); any Plcxd2 mutation (26 available)
Rorbtm1.1(cre)Hze mutation (1 available); any Rorb mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• dendritic spines of neurons shift toward a more mature phenotype, with a decrease in immature filopodia-type protrusions and a concomitant increase in mature mushroom-type spines indicating promotion of dendritic spine maturation
• neurons from mice injected with adenoviruses expressing TRE-DIO-FLPo and TRE-fDIO-tdTomato-IRES-tTA into the barrel cortex at P0 exhibit more spine apparatus-containing dendritic spines
• however, dendritic spine density is unaffected





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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
04/14/2026
MGI 6.24
The Jackson Laboratory