This allele from project Zfp329-7039J-F1199 was generated at The Jackson Laboratory by injecting Cas9 RNA and 2 guide sequences, AGTTGAGTGGCTTCCATGGA and CAAGAGATTTTATAAAGGTA, which resulted in a 13bp deletion beginning in exon 2 ATGGAAGCCACTC at Chromosome 7 negative strand position 12,811,259 bp ATGGAAGCCACTC (GRCm38) and ending after position 12,811,246 bp in exon 2. This mutation is predicted to cause amino acid sequence changes after 112 amino acid residues and early truncation 2 amino acids later. (J:188991)

Basic Information

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