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This allele produced from project TCPR0388 at TCP by injecting Cas9 mRNA and four guide RNAs with the spacer sequences TTTTAGTAGCGGCCATACTT, GAATTACCACTAATCTGCAT, GGCTATCTATCATCCGGACA, and ATTCTGCCGTCCTTACAGTA. This resulted in a 811-bp deletion from Chr5:117285622 to 117286432 insCA (GRCm38), exons ENSMUSE00000292490 & ENSMUSE00000292484. This mutation is predicted to cause a frameshift with amino acid changes after residue 47 and early truncation 11 amino acids later (p.M47Sfs*13). (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
