KEGG   VARIANT: 8733v1
Entry
8733v1                      Variant                                
Name
GPAA1 deficiency
Type
Loss of function
Gene
GPAA1  glycosylphosphatidylinositol anchor attachment 1 [KO:K05289]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 603048
Network
nt06018  GPI-anchor biosynthesis
Disease
H01489  Inherited glycosylphosphatidylinositol deficiencies
Reference
  Authors
Nguyen TTM, Murakami Y, Sheridan E, Ehresmann S, Rousseau J, St-Denis A, Chai G, Ajeawung NF, Fairbrother L, Reimschisel T, Bateman A, Berry-Kravis E, Xia F, Tardif J, Parry DA, Logan CV, Diggle C, Bennett CP, Hattingh L, Rosenfeld JA, Perry MS, Parker MJ, Le Deist F, Zaki MS, Ignatius E, Isohanni P, Lonnqvist T, Carroll CJ, Johnson CA, Gleeson JG, Kinoshita T, Campeau PM
  Title
Mutations in GPAA1, Encoding a GPI Transamidase Complex Protein, Cause Developmental Delay, Epilepsy, Cerebellar Atrophy, and Osteopenia.
  Journal
Am J Hum Genet 101:856-865 (2017)
DOI:10.1016/j.ajhg.2017.09.020
LinkDB

DBGET integrated database retrieval system