KEGG   VARIANT: 51645v1
Entry
51645v1                      Variant                               
Name
PPIL1 mutation
Type
Loss of function
Gene
PPIL1  peptidylprolyl isomerase like 1 [KO:K12733]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 601301
Network
nt06547  Spliceosome
Disease
H00897  Pontocerebellar hypoplasia
Reference
  Authors
Chai G, Webb A, Li C, Antaki D, Lee S, Breuss MW, Lang N, Stanley V, Anzenberg P, Yang X, Marshall T, Gaffney P, Wierenga KJ, Chung BH, Tsang MH, Pais LS, Lovgren AK, VanNoy GE, Rehm HL, Mirzaa G, Leon E, Diaz J, Neumann A, Kalverda AP, Manfield IW, Parry DA, Logan CV, Johnson CA, Bonthron DT, Valleley EMA, Issa MY, Abdel-Ghafar SF, Abdel-Hamid MS, Jennings P, Zaki MS, Sheridan E, Gleeson JG
  Title
Mutations in Spliceosomal Genes PPIL1 and PRP17 Cause Neurodegenerative Pontocerebellar Hypoplasia with Microcephaly.
  Journal
Neuron 109:241-256.e9 (2021)
DOI:10.1016/j.neuron.2020.10.035
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