About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Esrrbtm1.2Nat
targeted mutation 1.2, Jeremy Nathans
MGI:3720482
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Esrrbtm1.2Nat/Esrrbtm1.2Nat involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL MGI:3723506
cn2
Esrrbtm1.1Nat/Esrrbtm1.2Nat
Edil3Tg(Sox2-cre)1Amc/Edil3+
involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL MGI:3723508
cn3
Esrrbtm1.1Nat/Esrrbtm1.2Nat
Tg(Nes-cre)1Kln/0
involves: 129S6/SvEvTac * C57BL/6 * SJL MGI:3723507


Genotype
MGI:3723506
hm1
Allelic
Composition
Esrrbtm1.2Nat/Esrrbtm1.2Nat
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Esrrbtm1.2Nat mutation (0 available); any Esrrb mutation (211 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• no homozygous progeny are derived from Esrrbtm1.2 heterozygous matings




Genotype
MGI:3723508
cn2
Allelic
Composition
Esrrbtm1.1Nat/Esrrbtm1.2Nat
Edil3Tg(Sox2-cre)1Amc/Edil3+
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Edil3Tg(Sox2-cre)1Amc mutation (5 available); any Edil3 mutation (42 available)
Esrrbtm1.1Nat mutation (1 available); any Esrrb mutation (211 available)
Esrrbtm1.2Nat mutation (0 available); any Esrrb mutation (211 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• no auditory startle reflex
• observed beginning at several weeks of age
• adults spin or run in circles

hearing/vestibular/ear
• collapsed at 7 days of age
• reduction in volume seen at 4 days of age
• narrowing of membranous labyrinths of the three semicircular canals is observed in postnatal animals
• flattening of ampullae is observed postnatally




Genotype
MGI:3723507
cn3
Allelic
Composition
Esrrbtm1.1Nat/Esrrbtm1.2Nat
Tg(Nes-cre)1Kln/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Esrrbtm1.1Nat mutation (1 available); any Esrrb mutation (211 available)
Esrrbtm1.2Nat mutation (0 available); any Esrrb mutation (211 available)
Tg(Nes-cre)1Kln mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• loss of strial margenial cells in mutants is observed; this leads to loss of intraepithelial capillaries
• ABR thresholds are variably elevated between 1 and 3 months of age





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
05/07/2024
MGI 6.23
The Jackson Laboratory