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The allele contains a solitary long terminal repeat inserted into intron 4 that inserts an alternative splice donor site resulting in reduced transcript expression. The alternative splice donor site has been detected in A/J, AKR/J. C57BL/6NJ, FVB/NJ, NOD/ShiLtJ, and NZO/HlLtJ. It is absent in 129P2/OlaHsd, 129S1/SvImJ, 129S5/SvEvBrd, BALB/cJ, C3H/HeJ, CAST/EiJ, CBA/J, DBA2J, LP/J, PWK/PhJ, SPRET/EiJ, and WSB/EiJ. (J:321710)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
