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This allele produced from project TCPR0256 at The Centre for Phenogenomics by injecting Cas9 mRNA and one guide RNA with the spacer sequence GGTGCCAATGGGCCGGTGGC. This resulted in an insertion of 1 bp (A on the -1 strand) at Chr2:170406531 (GRCm38) in exon 4 (ENSMUSE00001221352). This mutation is predicted to cause a frameshift with amino acid changes after residue 169 and early truncation 6 amino acids later (p.T170Nfs*8). (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
