personality changes Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal shift in patterns of thinking, acting, or feeling. (Human Phenotype Ontology, HP_0000751)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000751
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Genes

17 genes associated with the personality changes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATP7B ATPase, Cu++ transporting, beta polypeptide
CHMP2B charged multivesicular body protein 2B
EIF2B1 eukaryotic translation initiation factor 2B, subunit 1 alpha, 26kDa
EIF2B2 eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa
EIF2B3 eukaryotic translation initiation factor 2B, subunit 3 gamma, 58kDa
EIF2B4 eukaryotic translation initiation factor 2B, subunit 4 delta, 67kDa
EIF2B5 eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa
GRN granulin
HTT huntingtin
LMNB1 lamin B1
MAPT microtubule-associated protein tau
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
PRNP prion protein
PSEN1 presenilin 1
TREM2 triggering receptor expressed on myeloid cells 2
TYROBP TYRO protein tyrosine kinase binding protein
VPS13A vacuolar protein sorting 13 homolog A (S. cerevisiae)