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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Neurod1tm1Mjts
targeted mutation 1, Ming-Jer Tsai
MGI:2148229
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Neurod1tm1Mjts/Neurod1tm1Mjts involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J MGI:4940063
hm2
Neurod1tm1Mjts/Neurod1tm1Mjts involves: 129S7/SvEvBrd * C57BL/6 MGI:2174973
hm3
Neurod1tm1Mjts/Neurod1tm1Mjts involves: 129X1/SvJ MGI:4940975
ht4
Neurod1tm1Kan/Neurod1tm1Mjts involves: 129P2/OlaHsd * 129S7/SvEvBrd MGI:3607798
cx5
Neurod1tm1Mjts/Neurod1tm1Mjts
Neurod6tm1Kan/Neurod6tm1Kan
involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J MGI:3850034


Genotype
MGI:4940063
hm1
Allelic
Composition
Neurod1tm1Mjts/Neurod1tm1Mjts
Genetic
Background
involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Neurod1tm1Mjts mutation (0 available); any Neurod1 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• ~30-40% of homozygotes die in the first postnatal week because of diabetes
• Background Sensitivity: when heterozygotes of a hybrid (129/SvEv x C57BL/6J) genetic background are crossed into the 129X1/SvJ background, about 60-70% of homozygotes survive to adulthood

behavior/neurological
• adult homozygotes display severe ataxia
• adult homozygotes exhibit swaying head movements
• adult homozygotes display hyperactivity
• adult homozygotes display circling
• homozygotes display a seizure disorder with both limbic and generalized features
• generalized tonic-clonic seizures occur occasionally, accompanied by either sustained cortical epileptiform discharges or intermittent abnormal synchronous discharges
• adult homozygotes display frequent (1-3 episodes/hour) spontaneous behavioral seizures that resemble those seen in models of limbic epilepsy
• typical episodes are brief (5-15 sec) with sudden focal dystonic posturing, flexor spasm of one or both forelimbs, and versive head movements
• episodic, brief freezing spells with tonic posturing are exacerbated by handling

nervous system
• homozygotes display a seizure disorder with both limbic and generalized features
• generalized tonic-clonic seizures occur occasionally, accompanied by either sustained cortical epileptiform discharges or intermittent abnormal synchronous discharges
• adult homozygotes display frequent (1-3 episodes/hour) spontaneous behavioral seizures that resemble those seen in models of limbic epilepsy
• typical episodes are brief (5-15 sec) with sudden focal dystonic posturing, flexor spasm of one or both forelimbs, and versive head movements
• episodic, brief freezing spells with tonic posturing are exacerbated by handling
• homozygotes show striking defects in hippocampal formation
• homozygotes show intact migration of mitotic precursor cells from the hippocampal neuroepithelium but fail to form the scaffolding of the dentate granule cell layer
• homozygotes lack an organized dentate gyrus
• a small, disorganized dentate cap contains a rudimentary population of cells, just separated from the CA3 pyramidal region, with some features of dentate granule neurons and other cells that resemble hilar interneurons
• a progressive decline in the number of mitotic (BrdUrd-labeled) precursor cells is seen in the dentate gyrus region from E16.5 to P4
• at E18.5, the forming upper blade of the mutant dentate is underpopulated with precursor cells and newly born granule cells, indicating impaired formation of the initial scaffolding of the dentate gyrus
• excessive cell death is seen in the dentate gyrus from P2 to P14; however, the specific identity of dying cells remains elusive
• homozygotes show no organized dentate hilus
• homozygotes lack the dentate granule cell layer
• at P5, the dentate gyrus consists only of a small mass of cells expressing calbindin with no orderly granule cell layer, contains significanlty fewer mitotic cells, and shows a low level of Prox-1 expression confined to the abnormal dentate cap, suggesting that differentiation of granule-like cells is delayed
• neurons born at the ventricular surface fail to express a specific dentate granule cell marker at the appropriate time during migration to the dentate gyrus
• at P5, differentiation of granule-like cells in the dentate cap appears to be delayed
• at P11, the tertiary matrix involutes and appears disorganized, similar to the abnormal structure present in adult mutant mice
• homozygotes display cerebellar defects that result in ataxia
• EEG activity during the spontaneous behavioral seizures consists of a stereotyped, rapid-burst discharge, followed by slower-interval synchronized spiking
• however, slow (theta) wave activity in the hippocampus remains normal

homeostasis/metabolism
N
• homozygotes that survive to adulthood show no ketonuria
• insulin levels return to normal values by 3 weeks of age
• homozygotes that survive to adulthood are slightly hyperglycemic




Genotype
MGI:2174973
hm2
Allelic
Composition
Neurod1tm1Mjts/Neurod1tm1Mjts
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Neurod1tm1Mjts mutation (0 available); any Neurod1 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• die 3-5 days after birth

growth/size/body
• smaller by 2 days after birth

digestive/alimentary system
• by 2 days of age, acinar cells lack the normal cellular polarity, with nuclei randomly distributed within the cell rather than in the basal region, overabundance of zymogen granules, and vacuolization characteristic of cellular degeneration
• secretin- and cholecystokinin-expressing enteroendocrine cells are absent in the intestine

homeostasis/metabolism
• seen at 2 days after birth
• dehydrated by 2 days after birth
• observe ketonuria at P2

endocrine/exocrine glands
• pancreas shows an increase in the number of apoptotic cells with no differences in cell proliferation
• by 2 days of age, acinar cells lack the normal cellular polarity, with nuclei randomly distributed within the cell rather than in the basal region, overabundance of zymogen granules, and vacuolization characteristic of cellular degeneration
• newborns show a 40% reduction in the number of alpha cells
• arrest in the expansion of the pancreatic beta-cell population occurring after E14.5 but prior to E17.5
• newborns show a 75% reduction in the number of beta cells
• newborns show a 20% reduction in the number of delta cells
• islets fail to develop at any stage of development in the pancreas
• endocrine cells form and aggregate as small clusters but fail to organize properly into mature islets

renal/urinary system
• observe ketonuria at P2

cellular
• pancreas shows an increase in the number of apoptotic cells with no differences in cell proliferation

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
type 1 diabetes mellitus 7 DOID:0110746 OMIM:600321
J:43010




Genotype
MGI:4940975
hm3
Allelic
Composition
Neurod1tm1Mjts/Neurod1tm1Mjts
Genetic
Background
involves: 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Neurod1tm1Mjts mutation (0 available); any Neurod1 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
respiratory system
• impaired alveolar formation secondary to reduced airspace epithelial proliferation
• at P5, proliferation of airway and alveolar epithelial cells in the developing airspace and airway of the mutant lung is reduced by 27% relative to wild-type controls
• however, lung epithelial differentiation is normal
• no differences in apoptosis are observed in the lung parenchyma
• at P5 and P10, the number of mutant pulmonary NEBs is significantly higher than that of wild-type controls
• however, the number of mutant pulmonary NEBs is fully normalized by 6 weeks of age
• at P5 and P10, distal airspace caliber is significantly increased relative to wild-type controls, as determined by mean linear intercept parameters
• no further increase in distal airspace caliber is noted after P10

endocrine/exocrine glands
• at P5 and P10, the number of mutant solitary PNECs is strikingly reduced relative to that in wild-type controls
• however, the number of mutant PNECs is fully normalized by 6 weeks of age

nervous system
• at P5 and P10, the number of mutant solitary PNECs is strikingly reduced relative to that in wild-type controls
• however, the number of mutant PNECs is fully normalized by 6 weeks of age




Genotype
MGI:3607798
ht4
Allelic
Composition
Neurod1tm1Kan/Neurod1tm1Mjts
Genetic
Background
involves: 129P2/OlaHsd * 129S7/SvEvBrd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Neurod1tm1Kan mutation (0 available); any Neurod1 mutation (29 available)
Neurod1tm1Mjts mutation (0 available); any Neurod1 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging




Genotype
MGI:3850034
cx5
Allelic
Composition
Neurod1tm1Mjts/Neurod1tm1Mjts
Neurod6tm1Kan/Neurod6tm1Kan
Genetic
Background
involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Neurod1tm1Mjts mutation (0 available); any Neurod1 mutation (29 available)
Neurod6tm1Kan mutation (0 available); any Neurod6 mutation (17 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• born at the expected ratio but rarely survive to the age of two days

growth/size/body
• overall growth is reduced

nervous system
• absence of demarcated granule cell layer
• ectopic aggregation of cells in the hilar region that fail to migrate to the dentate gyrus
• ectopic cells arrest during terminal differentiation
• increased number of cells that can fire only single non regenerative action potentials
• increased number of cells that can fire only single non regenerative action potentials
• ectopic granule cells have small Na+ currents





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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory