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COL4A5 c.1390G>A
ALS1
DMD c.1332-11868C>G
TP53
Amyotrophic Lateral Sclerosis 1
USH2A c.8559-2A>G
Cystic Fibrosis
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Gene editing
Shh
tm1(EGFP/cre)Cjt
Alias:
Shhgfp-Cre
Shhgfpcre
Shh
gfpcre
Shh
cre/Gfp
Shh-GFP-Cre
Shh
GFP-Cre
Shh-cre
Shh
CreEGFP
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Basic Information
Phenotypes
References Literature
A cassette containing an in frame fusion between GFP and cre was inserted at the ATG. Upon recombination, the first 35 base pairs after the ATG were deleted. Fluorescence was detected in the distal posterior region of E10-E12 embryos. (J:92504)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
3053959
Not Specified
Targeted
Insertion, Intragenic deletion
--
1
18
280
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
Title
PMID
Journal
Year
IF
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