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EN
This allele was generated at The Centre for Phenogenomics by electroporating Cas9 ribonucleoprotein complexes with single guide RNAs having spacer sequences of ATACTCGTATTAGGTATTGA targeting the 5' side and TGTAAAGGCATCGTGAAAAC targeting the 3' side of a critical region (ENSMUSE00000176809, ENSMUSE00000176812 and ENSMUSE00000176807). This resulted in a 8050-bp deletion of Chr3 from 138181167 to 138189216 (GRCm39) introducing a frameshift and premature stop codon. (J:265051)
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
