depression Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A condition characterized by pervasive dysphoric mood, loss of interests, and inability to experience pleasure. (Human Phenotype Ontology, HP_0000716)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000716
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Genes

35 genes associated with the depression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
ATP2A2 ATPase, Ca++ transporting, cardiac muscle, slow twitch 2
ATXN10 ataxin 10
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like
C10ORF2 chromosome 10 open reading frame 2
C9ORF72 chromosome 9 open reading frame 72
CLN6 ceroid-lipofuscinosis, neuronal 6, late infantile, variant
CPOX coproporphyrinogen oxidase
CSF1R colony stimulating factor 1 receptor
DCTN1 dynactin 1
DNAJC5 DnaJ (Hsp40) homolog, subfamily C, member 5
DRD2 dopamine receptor D2
FGF14 fibroblast growth factor 14
FMO3 flavin containing monooxygenase 3
FMR1 fragile X mental retardation 1
GBA glucosidase, beta, acid
GNAS GNAS complex locus
HMBS hydroxymethylbilane synthase
HTT huntingtin
JPH3 junctophilin 3
MECP2 methyl CpG binding protein 2
PANK2 pantothenate kinase 2
PDE11A phosphodiesterase 11A
PINK1 PTEN induced putative kinase 1
POLG polymerase (DNA directed), gamma
PPP2R2B protein phosphatase 2, regulatory subunit B, beta
PPT1 palmitoyl-protein thioesterase 1
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
PRKCG protein kinase C, gamma
PRNP prion protein
SGCE sarcoglycan, epsilon
SLC20A2 solute carrier family 20 (phosphate transporter), member 2
SPAST spastin
TBP TATA box binding protein
TBX1 T-box 1