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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Dscamtm1.1Kzy
targeted mutation 1.1, Kazuhiro Yamakawa
MGI:3840666
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Dscamtm1.1Kzy/Dscamtm1.1Kzy B6.129P2-Dscamtm1.1Kzy MGI:3840675
hm2
Dscamtm1.1Kzy/Dscamtm1.1Kzy involves: 129P2/OlaHsd * BALB/c * C57BL/6 MGI:3840677
ht3
Dscamtm1.1Kzy/Dscam+ B6.129P2-Dscamtm1.1Kzy MGI:3840676
ht4
Dscamtm1.1Kzy/Dscam+ involves: 129P2/OlaHsd * BALB/c * C57BL/6 MGI:3840678


Genotype
MGI:3840675
hm1
Allelic
Composition
Dscamtm1.1Kzy/Dscamtm1.1Kzy
Genetic
Background
B6.129P2-Dscamtm1.1Kzy
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dscamtm1.1Kzy mutation (1 available); any Dscam mutation (106 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice rarely survive more than 48 hours after birth
• administration of naloxone does not improve lethality
• Background Sensitivity: most mice die within 24 hours of birth unlike mice on a mixed 129P2/OlaHsd, BALB/c, and C57BL/6 background that survive into adulthood (J:146754)

respiratory system
• Background Sensitivity: under hypercapnic conditions, mice on a congenic C57BL/6 background exhibit reduced breathing frequency compared to similarly treated wild-type mice and unlike mice on a mixed 129P2/OlaHsd, BALB/c, and C57BL/6 background that exhibit a normal response to hypercapnia
• at birth, mice exhibit frequent apenic episodes unlike wild-type mice
• at birth, mice exhibit irregular respiratory rhythm and frequent apneic episodes unlike wild-type mice
• Background Sensitivity: mice exhibit irregular breathing patterns that are more severe than in mice on a mixed 129P2/OlaHsd, BALB/c, and C57BL/6 background

nervous system
• at E19, mice exhibit an increase the number of neurons in the medulla compared to in wild-type medulla
• irregular breathing pattern suggests defects of the central respiratory rhythm generator
• however, mice exhibit normal heart beats
• activity at the C4 ventral root is irregular unlike in wild-type mice that is more severe than in homozygotes
• the membrane potential trajectory of the pre-inspiratory neuron activity in the parafacial respiratory group during the pre-inspiratory phase is absent unlike in wild-type mice
• the synchronous inspiratory neuronal activities are weak and the neurons showing synchronous pre-inspiratory neuronal activities are not observed in the parafacial respiratory group unlike in wild-type mice
• the activities of the facial nerve become tonic and lose their synchroneity to the C4 activities unlike in wild-type mice




Genotype
MGI:3840677
hm2
Allelic
Composition
Dscamtm1.1Kzy/Dscamtm1.1Kzy
Genetic
Background
involves: 129P2/OlaHsd * BALB/c * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dscamtm1.1Kzy mutation (1 available); any Dscam mutation (106 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• Background Sensitivity: mice survive until adulthood unlike mice on a congenic C57BL/6 background that die shortly after birth

respiratory system
• Background Sensitivity: mice exhibit irregular breathing patterns that are milder than in mice on a congenic C57BL/6 background
• frequent

nervous system
• Background Sensitivity: C4 activities exhibit slower frequency and frequent apnea that is milder than in mice on a congenic C57BL/6 background
• however, pre-inspiratory neuronal activity is maintained unlike in mice on a congenic C57BL/6 background




Genotype
MGI:3840676
ht3
Allelic
Composition
Dscamtm1.1Kzy/Dscam+
Genetic
Background
B6.129P2-Dscamtm1.1Kzy
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dscamtm1.1Kzy mutation (1 available); any Dscam mutation (106 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
respiratory system
• mice exhibit an abnormal response to hypercapnia with excess expirations compared to similarly treated wild-type mice
• at birth, mice exhibit less severe abnormal respiratory rhythm compared to in homozygous mice

nervous system
• irregular breathing pattern suggests defects of the central respiratory rhythm generator
• however, mice exhibit normal heart beats
• activity at the C4 ventral root is irregular unlike in wild-type mice that is less severe than in homozygotes
• the membrane potential trajectory of the pre-inspiratory neuron activity in the parafacial respiratory group during the pre-inspiratory phase is reduced compared to in wild-type mice

reproductive system
• in 50% of pregnancies, delivery is delayed compared to in wild-type mice




Genotype
MGI:3840678
ht4
Allelic
Composition
Dscamtm1.1Kzy/Dscam+
Genetic
Background
involves: 129P2/OlaHsd * BALB/c * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dscamtm1.1Kzy mutation (1 available); any Dscam mutation (106 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
respiratory system
• Background Sensitivity: mice exhibit irregular breathing patterns that are milder than in mice on a congenic C57BL/6 background





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory