This allele was generated at The Jackson Laboratory by electroporating Cas9 protein and 2 guide sequences TTAGGTGGACTTGAGACCCC and GTAACTTGATCAATTTAGAG, which resulted in a 4121 bp deletion beginning at Chromosome 9 position 108,447,537 bp and ending after 108,451,657 bp (GRCm38/mm10). This mutation deletes ENSMUSE00000221526, ENSMUSE00000221528, ENSMUSE00000243289, ENSMUSE00000221530 and ENSMUSE00000221531 (exons 2-6) and 2120 bp of flanking and intronic sequence including the start site, splice acceptors, donors as well as 3 UTR and is predicted to result in a null allele. There is a 4 bp insertion ACCT at the deletion site. (J:188991)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6NJ
Endonuclease-mediated
Insertion, Intragenic deletion
Not Specified
1
2
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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
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