KEGG   VARIANT: 10844v1
Entry
10844v1                      Variant                               
Name
TUBGCP2 mutation
Type
Loss of function
Gene
TUBGCP2  gamma-tubulin complex component 2 isoform 2 [KO:K16569]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 617817
Network
nt06515  Regulation of kinetochore-microtubule interactions
Disease
H02606  Pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures
Reference
  Authors
Mitani T, Punetha J, Akalin I, Pehlivan D, Dawidziuk M, Coban Akdemir Z, Yilmaz S, Aslan E, Hunter JV, Hijazi H, Grochowski CM, Jhangiani SN, Karaca E, Fatih JM, Iwanowski P, Gambin T, Wlasienko P, Goszczanska-Ciuchta A, Bekiesinska-Figatowska M, Hosseini M, Arzhangi S, Najmabadi H, Rosenfeld JA, Du H, Marafi D, Blaser S, Teitelbaum R, Silver R, Posey JE, Ropers HH, Gibbs RA, Wiszniewski W, Lupski JR, Chitayat D, Kahrizi K, Gawlinski P
  Title
Bi-allelic Pathogenic Variants in TUBGCP2 Cause Microcephaly and Lissencephaly Spectrum Disorders.
  Journal
Am J Hum Genet 105:1005-1015 (2019)
DOI:10.1016/j.ajhg.2019.09.017
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