GLA c.548G>T ;(p.G183V)

Variant ID: X-100655745-C-A

NM_000169.2(GLA):c.548G>T;(p.G183V)

This variant was identified in 5 publications

View GRCh38 version.




Publications:


Abnormal Pre-mRNA Splicing in Exonic Fabry Disease-Causing GLA Mutations.

International Journal Of Molecular Sciences
Alfen, Franziska F; Putscher, Elena E; Hecker, Michael M; Zettl, Uwe Klaus UK; Hermann, Andreas A; Lukas, Jan J
Publication Date: 2022-12-03

Variant appearance in text: GLA: 548G>T; Gly183Val
PubMed Link: 36499585
Variant Present in the following documents:
  • Main text
  • ijms-23-15261.pdf
View BVdb publication page



Fabry disease in India: A multicenter study of the clinical and mutation spectrum in 54 patients.

Jimd Reports
Nampoothiri, Sheela S; Yesodharan, Dhanya D; Bhattacherjee, Amrita A; Ahamed, Hisham H; Puri, Ratna Dua RD; Gupta, Neerja N; Kabra, Madhulika M; Ranganath, Prajnya P; Bhat, Meenakshi M; Phadke, Shubha S; Radha Rama Devi, Akella A; Jagadeesh, Sujatha S; Danda, Sumita S; Sylaja, Padmavathy Narayana PN; Mandal, Kausik K; Bijarnia-Mahay, Sunita S; Makkar, Ravinder R; Verma, Ishwar Chander IC; Dalal, Ashwin A; Ramaswami, Uma U
Publication Date: 2020-11

Variant appearance in text: GLA: G183V
PubMed Link: 33204599
Variant Present in the following documents:
  • Main text
  • JMD2-56-82.pdf
View BVdb publication page



Assessment of Gene Variant Amenability for Pharmacological Chaperone Therapy with 1-Deoxygalactonojirimycin in Fabry Disease.

International Journal Of Molecular Sciences
Lukas, Jan J; Cimmaruta, Chiara C; Liguori, Ludovica L; Pantoom, Supansa S; Iwanov, Katharina K; Petters, Janine J; Hund, Christina C; Bunschkowski, Maik M; Hermann, Andreas A; Cubellis, Maria Vittoria MV; Rolfs, Arndt A
Publication Date: 2020-01-31

Variant appearance in text: GLA: 548G>T; G183V
PubMed Link: 32023956
Variant Present in the following documents:
  • Main text
  • ijms-21-00956.pdf
View BVdb publication page



Refinement of evolutionary medicine predictions based on clinical evidence for the manifestations of Mendelian diseases.

Scientific Reports
Šimčíková, Daniela D; Heneberg, Petr P
Publication Date: 2019-12-09

Variant appearance in text: GLA: G183V
PubMed Link: 31819097
Variant Present in the following documents:
  • 41598_2019_54976_MOESM2_ESM.xlsx, sheet 8
View BVdb publication page



Inhibition of Intermediate-Conductance Calcium-Activated K Channel (KCa3.1) and Fibroblast Mitogenesis by α-Linolenic Acid and Alterations of Channel Expression in the Lysosomal Storage Disorders, Fabry Disease, and Niemann Pick C.

Frontiers In Physiology
Oliván-Viguera, Aida A; Lozano-Gerona, Javier J; López de Frutos, Laura L; Cebolla, Jorge J JJ; Irún, Pilar P; Abarca-Lachen, Edgar E; García-Malinis, Ana J AJ; García-Otín, Ángel Luis ÁL; Gilaberte, Yolanda Y; Giraldo, Pilar P; Köhler, Ralf R
Publication Date: 2017

Variant appearance in text: GLA: G183V
PubMed Link: 28197106
Variant Present in the following documents:
  • Main text
  • fphys-08-00039.pdf
View BVdb publication page