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This allele from project TCPR0973 was generated at The Centre for Phenogenomics by electroporating Cas9 ribonucleoprotein complexes with single guide RNAs having spacer sequences of GAAGATCCAGGCCTCTTCGATGG, GCGCTATGGCATTAACACCACGG, CCTCGGAACTTCTCGGACAACCA, and GCATCTCAGGCCGGCATGACCGG targeting a critical region. This resulted in a inter-exon deletion of 909 bp Chr1:172505828 to 172506736; predicted to cause p.S84fs* (GRCm38). (J:237616)
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
