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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Unc119tm1Gina
targeted mutation 1, George Inana
MGI:3718005
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Unc119tm1Gina/Unc119tm1Gina involves: 129X1/SvJ * C57BL/6 MGI:3718399
ht2
Unc119tm1Gina/Unc119+ involves: 129X1/SvJ * C57BL/6 MGI:3718398


Genotype
MGI:3718399
hm1
Allelic
Composition
Unc119tm1Gina/Unc119tm1Gina
Genetic
Background
involves: 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Unc119tm1Gina mutation (0 available); any Unc119 mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• at 6 months, more apoptotic cells are present in the retina than in wild-type mice
• at 17 months, a burst of cell apoptosis occurs and continued through 20 months then decreases to almost none by 26 months
• mottling of the retinal pigment epithelium is first visible at 5 months of age and area of mottling increased with age
• blood vessels are thinned
• the outer nuclear layer (ONL) is thinned as early as 6 months, is slow in the first 13 months and accelerates at 17 months
• ONL is thinned down to almost nothing by 26 months
• at 7, 12 and 18 months mice exhibit photoreceptor and synapse degeneration
• at 20 months, severe retinal degeneration is present and reached end-stage by 26 months
• synapse degeneration is only present when photoreceptor degeneration occurs
• at 20 months, mice have significantly thinned retinas compared to wild-type mice
• beginning after 12 months mice have a reduction in a- and b-waves
• mice with severe degeneration have little to no electroretinogram reading
• at 15 months, residual b-waves are detected

pigmentation
• mottling of the retinal pigment epithelium is first visible at 5 months of age and area of mottling increased with age
• blood vessels are thinned




Genotype
MGI:3718398
ht2
Allelic
Composition
Unc119tm1Gina/Unc119+
Genetic
Background
involves: 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Unc119tm1Gina mutation (0 available); any Unc119 mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• after 17 months, one third of mice exhibit a partial thinning of the outer nuclear layer





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