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This allele was generated at The Jackson Laboratory by electroporating Cas9 protein and 2 guide sequences TTGTGACTCTGTTAGCTCGA and TTAAACTTGATCTAATCTTG, which resulted in a 1972 bp deletion beginning at Chromosome 11 position 16,952,904 bp and ending after 16,954,875 bp (GRCm38/mm10). This mutation deletes ENSMUSE00000442598, ENSMUSE00000344823, and ENSMUSE00000388108 (exons 2,3,and 4) and 910 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
