Source: ALL

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C4225200
Disease: COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 29 		disease 0.500 None 1.000 1 0 2016 2016
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0080178
Disease: Spina Bifida
Spina Bifida 		disease 0.310 None 1.000 1 0 2009 2009
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0038219
Disease: Status Dysraphicus
Status Dysraphicus 		disease 0.300 None 1.000 1 0 2009 2009
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0266508
Disease: Rachischisis
Rachischisis 		disease 0.300 None 1.000 1 0 2009 2009
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0011853
Disease: Diabetes Mellitus, Experimental
Diabetes Mellitus, Experimental 		disease 0.200 None 1.000 2 0 2004 2010
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0027055
Disease: Myocardial Reperfusion Injury
Myocardial Reperfusion Injury 		phenotype 0.200 None 1.000 1 0 2008 2008
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0035126
Disease: Reperfusion Injury
Reperfusion Injury 		disease 0.200 None 1.000 1 0 2009 2009
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C1277241
Disease: Delayed myelination
Delayed myelination 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0852413
Disease: Abnormal muscle tone
Abnormal muscle tone 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		disease 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0563243
Disease: Poor coordination
Poor coordination 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		disease 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0494475
Disease: Tonic - clonic seizures
Tonic - clonic seizures 		disease 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0241816
Disease: Global brain atrophy
Global brain atrophy 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C1806780
Disease: Increased CSF protein
Increased CSF protein 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C1833431
Disease: Subependymal cysts
Subependymal cysts 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C4553743
Disease: Spasticity, CTCAE
Spasticity, CTCAE 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C4280681
Disease: Gastrojejunal tube feeding in infancy
Gastrojejunal tube feeding in infancy 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C4021758
Disease: Delayed CNS myelination
Delayed CNS myelination 		disease 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C3806442
Disease: Myoclonic spasms
Myoclonic spasms 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C3149083
Disease: Decreased activity of mitochondrial complex III
Decreased activity of mitochondrial complex III 		phenotype 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C2677180
Disease: Congenital microcephaly
Congenital microcephaly 		disease 0.100 None 0 0
Entrez Id: 25828
Gene Symbol: TXN2
TXN2 		thioredoxin 2 0.628 0.615 2.6E-05
CUI: C1962966
Disease: Retinopathy, CTCAE
Retinopathy, CTCAE 		phenotype 0.100 None 0 0