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The mutation is the insertion of a gene-trap vector LacZ/Neo cassette into the intron between exons 7 and 8 of the gene. The LacZ reporter was not expressed in-frame. RT-PCR showed the complete loss of encoded transcripts in null mutant embryos. (J:232444)
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
