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CRISPR/Cas9 technology generated a 140-bp deletion from position +49,577 to +49,716 relative to the translation start site and comprises 53 nucleotides from exon 7 and 87 nucleotides of intron 7. This deletion causes skipping of exon 7 and alternative splicing of exon 6 to exon 8 to produce only the short isoform lacking exon 7. (J:343087)
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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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
