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This allele from project TCPR0641 was generated at The Centre for Phenogenomics by injecting Cas9 mRNA and four guide RNAs with spacer sequences of ATCACTGGTATAGGCTGGAT and ATGATCGGGTGCTTCAATCA targeting the 5' side and GGCAGATCGAGAGTCCTCAC and AAAGCGCGTGGAACGAGAAC targeting the 3' side of a critical region. This resulted in a 4,030-bp deletion of ChrX from 104084031 to 104088060. (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
