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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Neurog1-cre)1Jejo
transgene insertion 1, Jane E Johnson
MGI:4455179
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Mafbtm1.1Good/Mafbtm1Jeng
Tg(Neurog1-cre)1Jejo/0
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * SJL MGI:5581687
cn2
Gt(ROSA)26Sortm1(CAG-Mafb,-tdTomato)Good/Gt(ROSA)26Sor+
Tg(Neurog1-cre)1Jejo/0
involves: 129S4/SvJae * C57BL/6J * SJL/J MGI:5581688
cn3
Chd7Gt(S20-7E1)Sor/Chd7tm1.1Dmm
Gt(ROSA)26Sortm6(CAG-ZsGreen1)Hze/Gt(ROSA)26Sor+
Tg(Neurog1-cre)1Jejo/0
involves: 129S * C57BL/6 * SJL/J MGI:7518675


Genotype
MGI:5581687
cn1
Allelic
Composition
Mafbtm1.1Good/Mafbtm1Jeng
Tg(Neurog1-cre)1Jejo/0
Genetic
Background
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mafbtm1.1Good mutation (0 available); any Mafb mutation (18 available)
Mafbtm1Jeng mutation (0 available); any Mafb mutation (18 available)
Tg(Neurog1-cre)1Jejo mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• mice survive through adulthood

nervous system
N
• spiral ganglion neuron (SGN) processes organization and density are normal
• efferent innervation of cochlea is normal
• SGN firing properties are normal
• some are abnormally small or misshapen
• reduced numbers at P15
• failure of post-synpatic differentiation near the basolateral pole of the inner hair cells by P6
• impaired presynaptic development

hearing/vestibular/ear
N
• distortion product otoacoustic emissions are normal
• some are abnormally small or misshapen
• reduced numbers at P15
• dampened auditory brainstem response (ABR) waveforms and elevated auditory thresholds
• ABR wave I is delayed with increased latency compared to in control mice




Genotype
MGI:5581688
cn2
Allelic
Composition
Gt(ROSA)26Sortm1(CAG-Mafb,-tdTomato)Good/Gt(ROSA)26Sor+
Tg(Neurog1-cre)1Jejo/0
Genetic
Background
involves: 129S4/SvJae * C57BL/6J * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1(CAG-Mafb,-tdTomato)Good mutation (0 available); any Gt(ROSA)26Sor mutation (942 available)
Tg(Neurog1-cre)1Jejo mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• most mice die at 3 weeks of age of unknown causes

nervous system
N
• cochlear wiring and in spiral ganglion neuron firing properties are normal
• precocious basolateral localization of pre-synaptic ribbons in the hair cells
• however, the number of ribbons is normal
• afferent synapse development is accelerated in spiral ganglion neuron compared to in control mice

hearing/vestibular/ear
• precocious basolateral localization of pre-synaptic ribbons in the hair cells
• however, the number of ribbons is normal




Genotype
MGI:7518675
cn3
Allelic
Composition
Chd7Gt(S20-7E1)Sor/Chd7tm1.1Dmm
Gt(ROSA)26Sortm6(CAG-ZsGreen1)Hze/Gt(ROSA)26Sor+
Tg(Neurog1-cre)1Jejo/0
Genetic
Background
involves: 129S * C57BL/6 * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Chd7Gt(S20-7E1)Sor mutation (1 available); any Chd7 mutation (136 available)
Chd7tm1.1Dmm mutation (1 available); any Chd7 mutation (136 available)
Gt(ROSA)26Sortm6(CAG-ZsGreen1)Hze mutation (1 available); any Gt(ROSA)26Sor mutation (942 available)
Tg(Neurog1-cre)1Jejo mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• in the apical region of the cochlea aberrant axonal projections that cross, loop, and extend beyond the epithelium are seen
• at P1 total area of the spiral ganglion is reduced





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory