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This allele, from project TCPR0319, was generated at The Centre for Phenogenomics by injecting Cas9 mRNA and four guide RNAs with spacer sequences TCCACATTTTGCTCGGCTCA, CTGCGTTTTACCTTCCCCAA, GTACAGATTCATGGGCCCAC, and GCAGGCGGGTGTGAAGCATC. This resulted in a 686 bp deletion from Chr18:77847879 to 77848564 encompassing ENSMUSE00000514786. (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
