Neuronal Intranuclear Inclusion Disease Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
External Link	https://www.disgenet.org/browser/0/1/0/C1863843
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Genes

12 genes associated with the disease Neuronal Intranuclear Inclusion Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
ATXN1	ataxin 1
ATXN3	ataxin 3
DCTN4	dynactin 4 (p62)
FMR1	fragile X mental retardation 1
GGCT	gamma-glutamylcyclotransferase
GTF2H1	general transcription factor IIH, polypeptide 1, 62kDa
KHDRBS1	KH domain containing, RNA binding, signal transduction associated 1
LOC100996717	uncharacterized LOC100996717
NBPF19	neuroblastoma breakpoint family, member 19
NUP62	nucleoporin 62kDa
SQSTM1	sequestosome 1
SUMO1	small ubiquitin-like modifier 1