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This allele was generated at The Jackson Laboratory by electroporating Cas9 protein and 2 guide sequences GCATGCTGTGGGCAAGCAAG and AATGCATGTGGACAGCACTG, which resulted in a 481 bp deletion beginning at Chromosome 2 position 13,224,231 bp and ending after 13,224,711 bp (GRCm38/mm10). This mutation deletes ENSMUSE00001241282 (exon 4) and 360 bp of flanking intronic sequence including the splice acceptor and donor and is predicted to cause an early truncation after amino acid 54. (J:188991)
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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References Literature
Title
PMID
Journal
Year
IF
