H819PfsX5_human-DAGLA

General

Gene Locus : human-DAGLA

Mode of mutation : Natural mutant

Disease : Neuro-ocular DAGLA-related syndrome

Summary :

AAA Change :

Allelic Variant :

Risk Factor :

Inhibitor :

Structure :

Disease by interaction :

Interact Gene Locus :

Xenobiotic sensitivity :

Modification :

Torpedo_number : No torpedo number

Kinetic Parameter : No kinetic parameter

News : No news

Comment : c.2456_2457delAC, p.H819PfsX5 p.His819ProfsX5 Case 4: in a 5-year-old Caucasian male with global developmental delay, hypotonia, ataxia, dysarthria, nystagmus and low average intelligence

References (1)

Title : Endocannabinoid dysfunction in neurological disease: neuro-ocular DAGLA-related syndrome (NODRS) - Bainbridge_2022_Brain__
Author(s) : Bainbridge MN , Mazumder A , Ogasawara D , Abou Jamra R , Bernard G , Bertini E , Burglen L , Cope H , Crawford A , Derksen A , Dure L , Gantz E , Koch-Hogrebe M , Hurst ACE , Mahida S , Marshall P , Micalizzi A , Novelli A , Peng H , Rodriguez D , Robbins SL , Rutledge SL , Scalise R , Schliesske S , Shashi V , Srivastava S , Thiffault I , Topol S , Qebibo L , Wieczorek D , Cravatt B , Haricharan S , Torkamani A , Friedman J
Ref : Brain , : , 2022
Abstract : Bainbridge_2022_Brain__
ESTHER : Bainbridge_2022_Brain__
PubMedSearch : Bainbridge_2022_Brain__
PubMedID: 35737950
Gene_locus related to this paper: human-DAGLA