Frontal Cortical Atrophy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Atrophy of the frontal cortex. (Human Phenotype Ontology, HP_0006913)
External Link https://www.disgenet.org/browser/0/1/0/C4024965
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Genes

8 genes associated with the disease Frontal 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
CYB5A cytochrome b5 type A (microsomal)
CYB5R3 cytochrome b5 reductase 3
MEF2C myocyte enhancer factor 2C
PARS2 prolyl-tRNA synthetase 2, mitochondrial (putative)
PCDH19 protocadherin 19
POMT2 protein-O-mannosyltransferase 2
VCP valosin containing protein