KEGG   VARIANT: 10026v1
Entry
10026v1                      Variant                               
Name
PIGK deficiency
Gene
PIGK  phosphatidylinositol glycan anchor biosynthesis class K [KO:K05290]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 605087
Network
nt06018  GPI-anchor biosynthesis
Disease
H01489  Inherited glycosylphosphatidylinositol deficiencies
Reference
  Authors
Nguyen TTM, Murakami Y, Mobilio S, Niceta M, Zampino G, Philippe C, Moutton S, Zaki MS, James KN, Musaev D, Mu W, Baranano K, Nance JR, Rosenfeld JA, Braverman N, Ciolfi A, Millan F, Person RE, Bruel AL, Thauvin-Robinet C, Ververi A, DeVile C, Male A, Efthymiou S, Maroofian R, Houlden H, Maqbool S, Rahman F, Baratang NV, Rousseau J, St-Denis A, Elrick MJ, Anselm I, Rodan LH, Tartaglia M, Gleeson J, Kinoshita T, Campeau PM
  Title
Bi-allelic Variants in the GPI Transamidase Subunit PIGK Cause a Neurodevelopmental Syndrome with Hypotonia, Cerebellar Atrophy, and Epilepsy.
  Journal
Am J Hum Genet 106:484-495 (2020)
DOI:10.1016/j.ajhg.2020.03.001
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