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Exon 14 was replaced with a modified exon 14 in which nucleotide substitutions result in the amino acid substitutions of alanine for tryptophan and glutamic acid at positions 215 and 217, respectively (W215A, E217A). An Hprt gene was inserted downstream of the modified exon. (J:174629)
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 |
|---|
References Literature
Title
PMID
Journal
Year
IF
