KEGG   VARIANT: 3183v1
Entry
3183v1                      Variant                                
Name
HNRNPC mutation
Type
Loss of function
Gene
HNRNPC  heterogeneous nuclear ribonucleoprotein C [KO:K12884]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 164020
Network
nt06547  Spliceosome
Disease
H00773  Autosomal dominant intellectual developmental disorder
Reference
  Authors
Niggl E, Bouman A, Briere LC, Hoogenboezem RM, Wallaard I, Park J, Admard J, Wilke M, Harris-Mostert EDRO, Elgersma M, Bain J, Balasubramanian M, Banka S, Benke PJ, Bertrand M, Blesson AE, Clayton-Smith J, Ellingford JM, Gillentine MA, Goodloe DH, Haack TB, Jain M, Krantz I, Luu SM, McPheron M, Muss CL, Raible SE, Robin NH, Spiller M, Starling S, Sweetser DA, Thiffault I, Vetrini F, Witt D, Woods E, Zhou D, Elgersma Y, van Esbroeck ACM
  Title
HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder.
  Journal
Am J Hum Genet 110:1414-1435 (2023)
DOI:10.1016/j.ajhg.2023.07.005
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