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This allele produced from project TCPR0362 at TCP by injecting Cas9 mRNA and two guide RNAs with the spacer sequences CGGAACAGCCACCAGATGGT and CTGCAATTCCGAGATATACC. This resulted in an 894 bp deletion from Chr5:61809118 to 61810011, and ins 152bp in exon ENSMUSE00000409179. This mutation is predicted to cause a frameshift with amino acid changes after residue 80 and early truncation 12 amino acids later (p.I80Cfs*14). (GRCm38). (J:165963)
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
