This allele from project TCPR1106 was generated at The Centre for Phenogenomics by electroporating Cas9 ribonucleoprotein complexes with single guide RNAs having spacer sequences of CAGAGTACTGGTTAGAATCT and CCACATCAATCCTGTAGGTC targeting the 5' side and AGGCCTCAGTGTAACCGGGC and CTCGGGGTTCTAGCACGCTG targeting the 3' side of a critical exon. This resulted in a 686-bp del Chr13: 55012899 to 55013584, 12-bp del Chr13: 55013738 to 55013749 (GRCm38). (J:265051)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6NCrl
Endonuclease-mediated
Intragenic deletion
Not Specified
1
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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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Phenotypes

References Literature

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PMID
Journal
Year
IF
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