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EN
Exon 15 was replaced with one containing nucleotide substitutions that result in the amino acid substitution of alanine for aspartic acid at position 594 (D594). The modified exon 15 is preceded by a loxP site, a cDNA encoding exons 15 through 18, a termination sequence, and a floxed neo cassette. (J:161180)
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
