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Exons 1 and 2 of the Hprt gene along with a 3' loxP site and neo cassette were inserted into the coding region to create the starting point of a 1.3 Mb genomic deletion as a model for a 1.5 Mb hemizygous deletion in certain 22q11-deletion syndrome patients. (J:136969)
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
