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EN
Position 101,775,857 of chromosome 1 is fused to position 33,249,461 of chromosome 8. One extra base, T, is found in between the fused ends. The breakpoint on chromosome 1 falls in the first intron of Cntnap5b. No known genes are located near the breakpoint in chromosome 8. RT-PCR confirms the absence of Cntnap5b expression in brains from homozygous mice. (J:144618)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
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
