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This allele was generated at The Jackson Laboratory by electroporating Cas9 protein and 2 guide sequences GCAGGCACTAGATTATTCAG and AGCAGACTCCCACTCACAAG, which resulted in a 2400 bp deletion beginning at Chromosome 2 position 131,211,143 bp and ending after 131,213,542 bp (GRCm38/mm10). This mutation deletes ENSMUSE00000558540, ENSMUSE00001373302, ENSMUSE00000558538 (exons 2, 3, and 4) and 1210 bp of flanking intronic sequence including the start site, splice acceptor and donor and is predicted to result in a null allele. (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
