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This allele, from project TCPR0407, was generated at The Centre for Phenogenomics by injecting Cas9 mRNA and four guide RNAs with spacer sequences GAGTGTGGAGTGCGATAGTG, TGTCACACTAATGTCACTCG, GAGGTGCAAGCCTACCCTAG and TCCGAACTTCCTGCGGGAGC. This resulted in a 1,167 bp deletion from Chr18:50281278 to 50282444, encompassing ENSMUSE00000373759. (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
