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A promoterless IRES-lacZ-neo-loxP cassette replaced the translation start site and all of the first exon and about 300 bp of the first intron. Western blot analysis failed to detect protein in newborn mutants. Whole-embryo staining showed widespread expression, particularly within the peripheral nervous system, craniofacial region, dermis of the skin, and body cavities. (J:103753)
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
