Corticobasal Degeneration Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0393570
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Genes

33 genes associated with the disease Corticobasal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
APOE apolipoprotein E
BCHE butyrylcholinesterase
BDNF brain-derived neurotrophic factor
BPIFA2 BPI fold containing family A, member 2
C9ORF72 chromosome 9 open reading frame 72
CASP3 caspase 3, apoptosis-related cysteine peptidase
CHI3L1 chitinase 3-like 1 (cartilage glycoprotein-39)
CIT citron rho-interacting serine/threonine kinase
GRN granulin
IRS1 insulin receptor substrate 1
LRRK2 leucine-rich repeat kinase 2
MAPT microtubule-associated protein tau
MGC57346-CRHR1 MGC57346-CRHR1 readthrough
MOBP myelin-associated oligodendrocyte basic protein
MSMB microseminoprotein, beta-
NEFL neurofilament, light polypeptide
NGF nerve growth factor (beta polypeptide)
NOS1 nitric oxide synthase 1 (neuronal)
PSPH phosphoserine phosphatase
PSPN persephin
REG1A regenerating islet-derived 1 alpha
RIDA reactive intermediate imine deaminase A homolog
RMDN1 regulator of microtubule dynamics 1
RMDN2 regulator of microtubule dynamics 2
RMDN3 regulator of microtubule dynamics 3
SCRN1 secernin 1
SMUG1 single-strand-selective monofunctional uracil-DNA glycosylase 1
SNCA synuclein, alpha (non A4 component of amyloid precursor)
SOS1 son of sevenless homolog 1 (Drosophila)
SPPL2C signal peptide peptidase like 2C
STXBP3 syntaxin binding protein 3
SYBU syntabulin (syntaxin-interacting)
TARDBP TAR DNA binding protein