Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 18
Gene Symbol: ABAT
ABAT
0.400 Biomarker phenotype CTD_human 4-Aminobutyrate aminotransferase (GABA-transaminase) deficiency. 10407778 1999
Entrez Id: 18
Gene Symbol: ABAT
ABAT
0.400 Biomarker phenotype HPO
Entrez Id: 3553
Gene Symbol: IL1B
IL1B
0.310 AlteredExpression phenotype BEFREE Our results show that there are instances where memory consolidation can occur concurrently with elevated levels of IL-1ß in the hippocampus, fever, anorexia and lethargy during acute short-term sickness. 28212946 2017
Entrez Id: 3553
Gene Symbol: IL1B
IL1B
0.310 Biomarker phenotype CTD_human Mice lacking the Tak1 gene in brain endothelial cells showed a blunted fever response and reduced lethargy upon intravenous injection of the endogenous pyrogen IL-1β. 22143887 2011
Entrez Id: 10533
Gene Symbol: ATG7
ATG7
0.300 Biomarker phenotype CTD_human Autophagy limits proliferation and glycolytic metabolism in acute myeloid leukemia. 26568842 2015
Entrez Id: 9474
Gene Symbol: ATG5
ATG5
0.300 Biomarker phenotype CTD_human Autophagy limits proliferation and glycolytic metabolism in acute myeloid leukemia. 26568842 2015
Entrez Id: 1806
Gene Symbol: DPYD
DPYD
0.110 GeneticVariation phenotype BEFREE Two rare DPYD variants were associated with increased toxicity (Asp949Val with neutropenia, nausea and vomiting, diarrhoea and infection; IVS14+1G>A with lethargy, diarrhoea, stomatitis, hand-foot syndrome and infection; all ORs > 3). 30114658 2018
Entrez Id: 275
Gene Symbol: AMT
AMT
0.110 Biomarker phenotype BEFREE Nonketotic hyperglycinemia (NKH) is an inborn error of glycine degradation causing muscular hypotonia, seizures, apnea, and lethargy; it has a poor prognosis. 8657542 1996
Entrez Id: 2731
Gene Symbol: GLDC
GLDC
0.110 Biomarker phenotype BEFREE Nonketotic hyperglycinemia (NKH) is an inborn error of glycine degradation causing muscular hypotonia, seizures, apnea, and lethargy; it has a poor prognosis. 8657542 1996
Entrez Id: 1806
Gene Symbol: DPYD
DPYD
0.110 Biomarker phenotype HPO
Entrez Id: 2731
Gene Symbol: GLDC
GLDC
0.110 Biomarker phenotype HPO
Entrez Id: 275
Gene Symbol: AMT
AMT
0.110 Biomarker phenotype HPO
Entrez Id: 513
Gene Symbol: ATP5F1D
ATP5F1D
0.100 CausalMutation phenotype CLINVAR Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder. 29478781 2018
Entrez Id: 8891
Gene Symbol: EIF2B3
EIF2B3
0.100 Biomarker phenotype HPO
Entrez Id: 3767
Gene Symbol: KCNJ11
KCNJ11
0.100 Biomarker phenotype HPO
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2
0.100 Biomarker phenotype HPO
Entrez Id: 150094
Gene Symbol: SIK1
SIK1
0.100 Biomarker phenotype HPO
Entrez Id: 229
Gene Symbol: ALDOB
ALDOB
0.100 Biomarker phenotype HPO
Entrez Id: 4576
Gene Symbol: TRNT
TRNT
0.100 Biomarker phenotype HPO
Entrez Id: 34
Gene Symbol: ACADM
ACADM
0.100 Biomarker phenotype HPO
Entrez Id: 2561
Gene Symbol: GABRB2
GABRB2
0.100 Biomarker phenotype HPO
Entrez Id: 4720
Gene Symbol: NDUFS2
NDUFS2
0.100 Biomarker phenotype HPO
Entrez Id: 55005
Gene Symbol: RMND1
RMND1
0.100 Biomarker phenotype HPO
Entrez Id: 2592
Gene Symbol: GALT
GALT
0.100 Biomarker phenotype HPO
Entrez Id: 4594
Gene Symbol: MMUT
MMUT
0.100 Biomarker phenotype HPO