A kind of sgRNA guide sequence specifically targeting mouse galt gene and its application
A kind of specific, mouse technology, applied in the fields of medical genetics and molecular biology, can solve the problem of no sgRNA guide sequence knockout, and achieve the effect of high-efficiency screening, increase in quantity, and high concentration
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[0084] The principles and features of the present invention will be described below in conjunction with specific drawings, and the examples given are only used to explain the present invention, not to limit the scope of the present invention.
[0085] 1. Screening of human GALT gene pathogenic mutation sites, and confirming that human GALT gene c.904+1G is a pseudo-mutation site.
[0086] Type I galactosemia is caused by mutations in the GALT gene. First, the inactivation mutation of the human GALT gene was screened using the ExAC database, and a total of 19 mutation sites were screened (as shown in Table 1 and figure 1 shown); in order to more extensively screen the pathogenic mutations of GALT, the present invention also utilizes the OMIM online database to retrieve 17 kinds of GALT mutations (as shown in Table 2); then, the present invention utilizes the ClinVar database to retrieve splicing site mutations The disease-causing conditions (as shown in Table 3). In view of th...
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