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This allele from project TCPR0845 was generated at The Centre for Phenogenomics by electroporating Cas9 ribonucleoprotein complexes with single guide RNAs having spacer sequences of TAACGTTCCTTGCTGAAGAG and CTCTTTGTCGTGAGTCCCCT targeting the 5' side and GCTAAGAATGGCGTTCCCAG and TGAGCCTAGGAACACGGGAC targeting the 3' side leading to a 368-bp deletion from Chr18:77017405 to 77017772_insCCA (GRCm38). (J:237616)
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
