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This allele from project TCPR1137 was generated at The Centre for Phenogenomics by electroporating Cas9 ribonucleoprotein complexes with single guide RNAs having spacer sequences of GCTCCGCGAGTTGTTGGCGG, AAAAGACGTCCAGCGGCGAG and GGGTCCACGAGGTGGTGTAG targeting a critical exon. This resulted in a 36-bp deletion Chr19:46003690 to 46003725 and 2,084-bp del Chr19:46003853 to 46005936 (GRCm38). (J:265051)
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
