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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cdnftm1.1Uhb
targeted mutation 1.1, University of Helsinki, Biocenter
MGI:6394118
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cdnftm1.1Uhb/Cdnftm1.1Uhb either: B6JRcc.129P2(Cg)-Cdnftm1.1Uhb or (involves: 129P2/OlaHsd * C57BL/6JRcc * ICR) MGI:6400267


Genotype
MGI:6400267
hm1
Allelic
Composition
Cdnftm1.1Uhb/Cdnftm1.1Uhb
Genetic
Background
either: B6JRcc.129P2(Cg)-Cdnftm1.1Uhb or (involves: 129P2/OlaHsd * C57BL/6JRcc * ICR)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdnftm1.1Uhb mutation (0 available); any Cdnf mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• mice exhibit normal general architecture of midbrain dopaminergic neurons
• aged mice exhibit greater enteric neuron loss than wild-type mice
• reduced packing density of submucosal neurons
• however, mice exhibit normal enteric neuron apoptosis rates, packing density of myenteric neurons and density of glia
• hypoplasia in 1.5 month mice and persisting through adulthood
• of enteric neurons in the submucosal plexus of the duodenum, ileum, and colon
• reduced dopamine re-uptake by dopamine transporter at 6 months of age
• however, dopamine release is normal

homeostasis/metabolism
N
• mice exhibit normal blood glucose levels
• in submucosal enteric neurons
• however, autophagy is normal in the myenteric plexus
• reduced dopamine re-uptake by dopamine transporter at 6 months of age
• however, dopamine release is normal
• amphetamine-induced, especially in 9 to 12 month old mice

behavior/neurological
• enhanced amphetamine-induced hyperlocomotion in 7 to 9 month old mice

cellular
• in submucosal enteric neurons
• however, autophagy is normal in the myenteric plexus

growth/size/body
N
• exhibit normal growth and weight





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