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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nmnat2Tn(sb-Tyr)2172.P9KK4BOve
targeted mutation 2172.P9KK4B, Paul A Overbeek
MGI:5473270
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Nmnat2Tn(sb-Tyr)2172.P9KK4BOve/Nmnat2Tn(sb-Tyr)2172.P9KK4BOve involves: FVB/N MGI:5473285


Genotype
MGI:5473285
hm1
Allelic
Composition
Nmnat2Tn(sb-Tyr)2172.P9KK4BOve/Nmnat2Tn(sb-Tyr)2172.P9KK4BOve
Genetic
Background
involves: FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nmnat2Tn(sb-Tyr)2172.P9KK4BOve mutation (0 available); any Nmnat2 mutation (271 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Distended bladder, urogenital tract damage, underdeveloped diaphragm, and decreased skeletal muscle mass in Nmnat2Tn(sb-Tyr)2172.P9KK4BOve/Nmnat2Tn(sb-Tyr)2172.P9KK4BOve E18.5 pups

mortality/aging

nervous system
• decreased motor neurons
• 2- to 3-fold increase in pyknotic neurons in the spinal cord at E13.5
• in facial and other nuclei
• in the dorsal root ganglion
• in the spinal cord as early as E13.5
• in the dorsal root ganglion in the lumbar region at E18.5
• axon loss in the leg begins between E13 and E15
• axon loss in the leg begins between E13 and E15

renal/urinary system
• underdeveloped
• damaged due to urine retention
• in full-term pups
• suggested by kidney underdevelopment and damage

respiratory system

muscle

behavior/neurological
• in full-term pups
• in full-term pups

growth/size/body
• in full-term pups





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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
11/19/2024
MGI 6.24
The Jackson Laboratory