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This allele, from project TCPR0246, was generated at The Centre for Phenogenomics by injecting Cas9 mRNA and one guide RNA with spacer sequence AGTCGTTCATGTGCCAACGT. This resulted in a 1 bp insertion at Chr2:66319540 in OTTMUSE00000158516. This mutation is predicted to cause a frameshift with amino acid changes after residue 932 and early truncation 63 amino acids later (p.W932Lfs*65). (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
