About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ncaldtm1.1(KOMP)Vlcg
targeted mutation 1.1, Velocigene
MGI:5468989
Summary 3 genotypes


Genotype
MGI:6360464
hm1
Allelic
Composition
Ncaldtm1.1(KOMP)Vlcg/Ncaldtm1.1(KOMP)Vlcg
Genetic
Background
B6N(Cg)-Ncaldtm1.1(KOMP)Vlcg/J
Cell Lines 15762A-A6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ncaldtm1.1(KOMP)Vlcg mutation (1 available); any Ncald mutation (20 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• at 5 months of age, body weight of males is significantly lower than that of wild-type controls

nervous system
• in culture, spinal motor neurons (MNs) isolated from E13.5 homozygous mutant embryos show a significant increase in the average axon length and secondary axonal branching relative to wild-type spinal MNs
• interestingly, homozygous spinal MNs have significantly shorter axons than those isolated from heterozygous mutant embryos
• however, hippocampal neurons axonal length is normal
• homozygotes exhibit disturbed adult neurogenesis in the hippocampus; in the dentate gyrus, the intensity of doublecortin (DCX, a marker for newly differentiated and immature cells) is significantly increased P14, unaltered at P30, and significantly reduced at 4 months of age relative to wild-type controls
• DCX+ neuronal density is significantly reduced at 4 months of age
• homozygotes exhibit a brain maturation defect during adolescence
• however, no signs of astrogliosis are observed, and cortical layering, cortical thickness, corpus callosum thickness, overall neuronal cell density and neuronal complexity remain normal at 4 month of age
• at 4 months of age, brain is significantly smaller than normal
• at 4 months of age, brain weight is significantly lower than that of wild-type controls
• however, no significant change in brain weight is noted at P14 and at P30, and brain-to-body mass ratio is normal at 4 months
• adult brains show significantly enlarged lateral ventricles
• adult brains show significantly increased volume of lateral ventricles
• adult brains show abnormal hippocampal morphology
• adult brains display a significantly reduced subgranular zone length (SGZ)
• however, SGZ length appears unaffected when normalized to hippocampal volume, and overall cell proliferation as well as neuroblast proliferation in the dentate gyrus are normal
• adult hippocampi are generally smaller than normal
• at 4 months of age, the number of DCX+ newborn neurons in the dentate gyrus is significantly decreased
• however, no increase in apoptotic cell death is observed
• 4-month-old brain lysates show a significant increase in JNK signaling relative to wild-type controls
• the few DCX+ newborn neurons found in the dentate gyrus at 4 months of age show a tangential orientation rather than integration in the granule cell layer, suggesting a possible migration defect
• myelin basic protein (MBP) levels are significantly reduced in lysates derived from P30 brains; however, normal MBP levels are detected in lysates from 4-mo-old brains, suggesting a delay in myelination
• however, neurofilament levels are normal suggesting that axon number is unaffected

cellular
• in culture, spinal motor neurons (MNs) isolated from E13.5 homozygous mutant embryos show a significant increase in the average axon length and secondary axonal branching relative to wild-type spinal MNs
• interestingly, homozygous spinal MNs have significantly shorter axons than those isolated from heterozygous mutant embryos
• however, hippocampal neurons axonal length is normal
• homozygotes exhibit disturbed adult neurogenesis in the hippocampus; in the dentate gyrus, the intensity of doublecortin (DCX, a marker for newly differentiated and immature cells) is significantly increased P14, unaltered at P30, and significantly reduced at 4 months of age relative to wild-type controls
• DCX+ neuronal density is significantly reduced at 4 months of age
• the few DCX+ newborn neurons found in the dentate gyrus at 4 months of age show a tangential orientation rather than integration in the granule cell layer, suggesting a possible migration defect

reproductive system
• homozygotes exhibit a lower fertility rate




Genotype
MGI:5631338
hm2
Allelic
Composition
Ncaldtm1.1(KOMP)Vlcg/Ncaldtm1.1(KOMP)Vlcg
Genetic
Background
C57BL/6N-Ncaldtm1.1(KOMP)Vlcg/J
Cell Lines 15762A-A6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ncaldtm1.1(KOMP)Vlcg mutation (1 available); any Ncald mutation (20 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype



Genotype
MGI:6360465
ht3
Allelic
Composition
Ncaldtm1.1(KOMP)Vlcg/Ncald+
Genetic
Background
B6N(Cg)-Ncaldtm1.1(KOMP)Vlcg/J
Cell Lines 15762A-A6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ncaldtm1.1(KOMP)Vlcg mutation (1 available); any Ncald mutation (20 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• heterozygotes exhibit normal brain weight and brain morphology at 4 months of age
• both DCX+ neuronal density and DCX intensity are normal in the dentate gyrus, indicating normal adult neurogenesis
• JNK activation is normal
• in culture, spinal motor neurons (MNs) isolated from E13.5 heterozygous mutant embryos show a significant increase in the average axon length and secondary axonal branching relative to wild-type spinal MNs
• heterozygous spinal MNs have significantly longer axons than those isolated from homozygous mutant embryos
• however, hippocampal neurons axonal length is normal

cellular
• in culture, spinal motor neurons (MNs) isolated from E13.5 heterozygous mutant embryos show a significant increase in the average axon length and secondary axonal branching relative to wild-type spinal MNs
• heterozygous spinal MNs have significantly longer axons than those isolated from homozygous mutant embryos
• however, hippocampal neurons axonal length is normal

growth/size/body
N
• heterozygotes exhibit normal body weight at 4 months of age





Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/19/2024
MGI 6.24
The Jackson Laboratory