Gene Locus : human-ABHD12
Mode of mutation : Natural mutant
Disease : PHARC Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract
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 : JANUARY-02-2013
Comment :
Nonsense Homozygous p.Arg65* c.193C>T Exon 2, Mutation found in a patient initially diagnosed with Usher syndrome type 3
| Title : The Phenotypic Spectrum of Patients with PHARC Syndrome Due to Variants in ABHD12: An Ophthalmic Perspective - Nguyen_2021_Genes.(Basel)_12_1404 |
| Author(s) : Nguyen XT , Almushattat H , Strubbe I , Georgiou M , Li CHZ , van Schooneveld MJ , Joniau I , De Baere E , Florijn RJ , Bergen AA , Hoyng CB , Michaelides M , Leroy BP , Boon CJF |
| Ref : Genes (Basel) , 12 :1404 , 2021 |
| Abstract : |
| PubMedSearch : Nguyen_2021_Genes.(Basel)_12_1404 |
| PubMedID: 34573385 |
| Gene_locus related to this paper: human-ABHD12 |
| Title : Expanding the clinical phenotype in patients with disease causing variants associated with atypical Usher syndrome - Igelman_2021_Ophthalmic.Genet_42_664 |
| Author(s) : Igelman AD , Ku C , da Palma MM , Georgiou M , Schiff ER , Lam BL , Sankila EM , Ahn J , Pyers L , Vincent A , Ferraz Sallum JM , Zein WM , Oh JK , Maldonado RS , Ryu J , Tsang SH , Gorin MB , Webster AR , Michaelides M , Yang P , Pennesi ME |
| Ref : Ophthalmic Genet , 42 :664 , 2021 |
| Abstract : |
| PubMedSearch : Igelman_2021_Ophthalmic.Genet_42_664 |
| PubMedID: 34223797 |
| Gene_locus related to this paper: human-ABHD12 |
| Title : Targeted next-generation sequencing identifies a homozygous nonsense mutation in ABHD12, the gene underlying PHARC, in a family clinically diagnosed with Usher syndrome type 3 - Eisenberger_2012_Orphanet.J.Rare.Dis_7_59 |
| Author(s) : Eisenberger T , Slim R , Mansour A , Nauck M , Nurnberg G , Nurnberg P , Decker C , Dafinger C , Ebermann I , Bergmann C , Bolz H |
| Ref : Orphanet J Rare Dis , 7 :59 , 2012 |
| Abstract : |
| PubMedSearch : Eisenberger_2012_Orphanet.J.Rare.Dis_7_59 |
| PubMedID: 22938382 |
| Gene_locus related to this paper: human-ABHD12 |