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The cDNA for human PDCD1, encompassing sequence from kozak through translational stop and the last 2 exons of a mouse metallothionein gene including the terminal intron followed by a neo mini-gene flanked by loxP sites replaced the coding portion of murine exon 1 in order to maintain correct splicing of the fusion transcript. Flow cytometric protein expression analysis confirmed absence of targeted protein expression. (J:126829)
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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References Literature
Title
PMID
Journal
Year
IF
