memory impairment Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An impairment of memory as manifested by a reduced ability to remember things such as dates and names, and increased forgetfulness. (Human Phenotype Ontology, HP_0002354)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002354
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Genes

70 genes associated with the memory impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
APP amyloid beta (A4) precursor protein
C4A complement component 4A (Rodgers blood group)
CECR1 cat eye syndrome chromosome region, candidate 1
CHMP2B charged multivesicular body protein 2B
COX1
COX2
COX3
CP ceruloplasmin (ferroxidase)
CSF1R colony stimulating factor 1 receptor
CTSH cathepsin H
DNMT1 DNA (cytosine-5-)-methyltransferase 1
ECM1 extracellular matrix protein 1
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
FGF14 fibroblast growth factor 14
FMR1 fragile X mental retardation 1
GRN granulin
HCRT hypocretin (orexin) neuropeptide precursor
HLA-B major histocompatibility complex, class I, B
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
IL10 interleukin 10
IL12RB2 interleukin 12 receptor, beta 2
IL23R interleukin 23 receptor
KCNQ2 potassium channel, voltage gated KQT-like subfamily Q, member 2
KCNQ3 potassium channel, voltage gated KQT-like subfamily Q, member 3
MAPT microtubule-associated protein tau
MEFV Mediterranean fever
MLH1 mutL homolog 1
MOG myelin oligodendrocyte glycoprotein
MSH2 mutS homolog 2
MSH6 mutS homolog 6
MT-ND4 NADH dehydrogenase, subunit 4 (complex I)
MT-ND5 NADH dehydrogenase, subunit 5 (complex I)
MT-ND6 NADH dehydrogenase, subunit 6 (complex I)
MT-TF tRNA
MT-TH tRNA
MT-TL1 tRNA
MT-TQ tRNA
MT-TS1 tRNA
MT-TS2 tRNA
MT-TW tRNA
MYD88 myeloid differentiation primary response 88
ND1
NOD2 nucleotide-binding oligomerization domain containing 2
NOTCH3 notch 3
P2RY11 purinergic receptor P2Y, G-protein coupled, 11
PAH phenylalanine hydroxylase
PMS2 PMS2 postmeiotic segregation increased 2 (S. cerevisiae)
PRKCG protein kinase C, gamma
PRNP prion protein
PRRT2 proline-rich transmembrane protein 2
PSEN1 presenilin 1
SCN2A sodium channel, voltage gated, type II alpha subunit
SLC20A2 solute carrier family 20 (phosphate transporter), member 2
SPAST spastin
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)
STAT4 signal transducer and activator of transcription 4
TLR4 toll-like receptor 4
TNFSF4 tumor necrosis factor (ligand) superfamily, member 4
TREM2 triggering receptor expressed on myeloid cells 2
TREX1 three prime repair exonuclease 1
TYROBP TYRO protein tyrosine kinase binding protein
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1
VAMP1 vesicle-associated membrane protein 1 (synaptobrevin 1)
VPS13A vacuolar protein sorting 13 homolog A (S. cerevisiae)
ZNF365 zinc finger protein 365