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Exon 13 was replaced with one in which nucleotide substitutions (CTGCGCCGG to GCGCGCCAA) results in the amino acid substitution of alanine for leucine at positions 1298 (L1298A) and glutamine for arginine at position 1300 (Q1300R). Cre-mediated recombination removed the floxed neo cassette inserted downstream of the modified exon 13. (J:181943)
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
