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Phenotypes Associated with This Genotype
Genotype
MGI:6383926
Allelic
Composition
Ncam1tm1Cgn/Ncam1tm1Cgn
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ncam1tm1Cgn mutation (1 available); any Ncam1 mutation (65 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• at 18 months
• however, the number of optic nerve axons is normal at 2 and 18 months
• at 2 months
• however, the number of optic nerve axons is normal at 2 and 18 months
• in middle and peripheral regions at 2 months
• increased at 2 months
• loss of one third of thickness in the central areas at 18 months
• increased retinal thickness only in the peripheral temporal region at 2 months
• reduced retinal thickness in the central areas at 18 months
• however, mice exhibit normal thickness in the inner nuclear layer, outer plexiform layer and outer nuclear layer at 2 months
• a-wave Vmax is more than double wild-type before falling to normal levels by 10 months and older
• b-wave V-max is more than double at 2 months then falls to normal levels by 10 months or older with premature loss of light sensitivity at 18 months
• however, mice exhibit normal retinal sensitivity and b-wave to a-wave ratio
• premature loss of visual detection
• no ability to detect pattern at any age

nervous system
• at 18 months
• however, the number of optic nerve axons is normal at 2 and 18 months
• at 2 months
• however, the number of optic nerve axons is normal at 2 and 18 months


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)
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last database update
05/21/2024
MGI 6.23
The Jackson Laboratory