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Grant: Project Grant

Ottawa Hospital Research Institute

$822,376.00

Defining the role of the chromatin modifying protein PHF6 during normal and pathological cognitive development

EF 2017-18

Résumé
Inherited mutations in the PHF6 gene result in a rare childhood disorder that is associated with moderate to severe intellectual disability. In addition, acquired mutations in the PHF6 gene are associated with the development of several different types of leukemia. These studies indicate the importance of the PHF6 protein yet how mutations cause these different diseases remains largely unknown. We have recently generated mice that contain one of the same mutations in the Phf6 gene that is commonly found in both human conditions. Here, we propose to characterize the phenotype of these mice to gain additional insight into the function of the Phf6 gene during normal and pathological cognitive development.
Programme
Project Grant
Emplacement
Ontario, Canada
Type de bénéficiaire
Other
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
381573
Name
Picketts David J
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Genetics
Projecttitle
Defining the role of the chromatin modifying protein PHF6 during normal and pathological cognitive development
Programtype2
Operating Grants
Orgnameinp2
Ottawa Hospital Research Institute
Cihramount2
$822,376
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Epigenetics; Intellectual Disability; Nervous System Development; Neurodevelopmental Disorder; Transgenic Mice
Abstract
Inherited mutations in the PHF6 gene result in a rare childhood disorder that is associated with moderate to severe intellectual disability. In addition, acquired mutations in the PHF6 gene are associated with the development of several different types of leukemia. These studies indicate the importance of the PHF6 protein yet how mutations cause these different diseases remains largely unknown. We have recently generated mice that contain one of the same mutations in the Phf6 gene that is commonly found in both human conditions. Here, we propose to characterize the phenotype of these mice to gain additional insight into the function of the Phf6 gene during normal and pathological cognitive development.
Competitiondate
201803
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Picketts, David J
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $822,376~ $0~