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This allele from project TCPR0786 was generated at The Centre for Phenogenomics by electroporating Cas9 ribonucleoprotein complexes with single guide RNAs having spacer sequences of CTGCTAGGACAAGGCCGAGC and AGTGGGTGCGCCGACACCGC targeting the 5' side and AGGGCCTTGTCACTCTAGGG and CAATGGCAGTCATATAGACT targeting the 3' side of exon ENSMUSE00000535007. This resulted in a 760-bp deletion of Chr9 from 52126471 to 52127230 (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
