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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Syne2cpfl8-2J
cone photoreceptor function loss 8, 2 Jackson
MGI:6358246
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Syne2cpfl8-2J/Syne2cpfl8-2J B6;129-Syne2cpfl8-2J/Boc MGI:6358250


Genotype
MGI:6358250
hm1
Allelic
Composition
Syne2cpfl8-2J/Syne2cpfl8-2J
Genetic
Background
B6;129-Syne2cpfl8-2J/Boc
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Syne2cpfl8-2J mutation (0 available); any Syne2 mutation (297 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• at 3 weeks of age the fundus shows areas of hypo- and hyper-pigmentation and attenuated vessels
• slight reduction in thickness at 3 months of age
• rod photoreceptors are mislocated in the inner nuclear layer at 3 months of age
• at 3 weeks of age by optical coherence tomography
• diminished cone b-wave ERG response at 3 weeks of age

cardiovascular system





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
11/12/2024
MGI 6.24
The Jackson Laboratory