Temporal Cortical Atrophy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Atrophy of the temporal cortex. (Human Phenotype Ontology, HP_0007112)
External Link https://www.disgenet.org/browser/0/1/0/C4024936
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Genes

13 genes associated with the disease Temporal Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
C9ORF72 chromosome 9 open reading frame 72
CHMP2B charged multivesicular body protein 2B
COG1 component of oligomeric golgi complex 1
CYB5A cytochrome b5 type A (microsomal)
CYB5R3 cytochrome b5 reductase 3
GRN granulin
MAPT microtubule-associated protein tau
PCDH19 protocadherin 19
PDE6D phosphodiesterase 6D, cGMP-specific, rod, delta
PSEN1 presenilin 1
TMEM106B transmembrane protein 106B
TREM2 triggering receptor expressed on myeloid cells 2
VCP valosin containing protein