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EN
This allele from project TCPR0903 was generated at The Centre for Phenogenomics by electroporating Cas9 ribonucleoprotein complexes with single guide RNAs having spacer sequences of CAGGGTATATGAGCATTAAT and GTCGTGACACCCAGCTTAGA targeting the 5' side and CGTGGCCACGCGCTGTAATC and GTGGGCCACTCGTTCATCCC targeting the 3' side of exon ENSMUSE00001230926. This resulted in a 1794-bp deletion of Chr17 from 70655896 to 70657689 (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
