Source: ANIMAL_MODELS

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: 7040
Gene Symbol: TGFB1
TGFB1 		transforming growth factor beta 1 0.287 0.962 3.7E-02
CUI: C0740392
Disease: Infarction, Middle Cerebral Artery
Infarction, Middle Cerebral Artery 		disease 0.200 None 1.000 1 0 2020 2020
Entrez Id: 8140
Gene Symbol: SLC7A5
SLC7A5 		solute carrier family 7 member 5 0.513 0.808 0.24
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		disease 0.210 None 1.000 0 0 2020 2020
Entrez Id: 115948
Gene Symbol: CCDC151
CCDC151 		coiled-coil domain containing 151 0.659 0.577 3.5E-15
CUI: C0265747
Disease: Congenital atresia of nasopharynx
Congenital atresia of nasopharynx 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 115948
Gene Symbol: CCDC151
CCDC151 		coiled-coil domain containing 151 0.659 0.577 3.5E-15
CUI: C0478019
Disease: Other specified congenital malformations of respiratory system
Other specified congenital malformations of respiratory system 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 122618
Gene Symbol: PLD4
PLD4 		phospholipase D family member 4 0.780 0.500 7.7E-13
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		disease 0.210 None 1.000 1 0 2019 2019
Entrez Id: 1241
Gene Symbol: LTB4R
LTB4R 		leukotriene B4 receptor 0.576 0.692 0.12
CUI: C0027719
Disease: Nephrosclerosis
Nephrosclerosis 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 128178
Gene Symbol: EDARADD
EDARADD 		EDAR associated death domain 0.638 0.462 3.2E-04
CUI: C0029882
Disease: Otitis Media
Otitis Media 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 137392
Gene Symbol: FAM92A
FAM92A 		family with sequence similarity 92 member A 0.729 0.308 5.8E-08
CUI: C0152427
Disease: Polydactyly
Polydactyly 		disease 0.210 None 1.000 1 0 2019 2019
Entrez Id: 137392
Gene Symbol: FAM92A
FAM92A 		family with sequence similarity 92 member A 0.729 0.308 5.8E-08
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL 		disease 0.510 None 1.000 1 0 2019 2019
Entrez Id: 196500
Gene Symbol: PIANP
PIANP 		PILR alpha associated neural protein 0.931 0.038 0.38
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 24145
Gene Symbol: PANX1
PANX1 		pannexin 1 0.575 0.846 2.5E-06
CUI: C0085548
Disease: Autosomal Recessive Polycystic Kidney Disease
Autosomal Recessive Polycystic Kidney Disease 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 2952
Gene Symbol: GSTT1
GSTT1 		glutathione S-transferase theta 1 0.393 0.923 1.5E-04
CUI: C0028754
Disease: Obesity
Obesity 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 3766
Gene Symbol: KCNJ10
KCNJ10 		potassium inwardly rectifying channel subfamily J member 10 0.599 0.654 0.15
CUI: C0270857
Disease: Epilepsy, Reflex
Epilepsy, Reflex 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 406957
Gene Symbol: MIR181C
MIR181C 		microRNA 181c 0.555 0.769
CUI: C0023903
Disease: Liver neoplasms
Liver neoplasms 		group 0.200 None 1.000 1 0 2019 2019
Entrez Id: 406957
Gene Symbol: MIR181C
MIR181C 		microRNA 181c 0.555 0.769
CUI: C0206624
Disease: Hepatoblastoma
Hepatoblastoma 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 406957
Gene Symbol: MIR181C
MIR181C 		microRNA 181c 0.555 0.769
CUI: C0345904
Disease: Malignant neoplasm of liver
Malignant neoplasm of liver 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 406957
Gene Symbol: MIR181C
MIR181C 		microRNA 181c 0.555 0.769
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		disease 0.220 None 1.000 1 0 2019 2019
Entrez Id: 406957
Gene Symbol: MIR181C
MIR181C 		microRNA 181c 0.555 0.769
CUI: C2676033
Disease: Hepatoblastoma Caused By Somatic Mutation
Hepatoblastoma Caused By Somatic Mutation 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 407015
Gene Symbol: MIR26A1
MIR26A1 		microRNA 26a-1 0.653 0.577
CUI: C0022660
Disease: Kidney Failure, Acute
Kidney Failure, Acute 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 407015
Gene Symbol: MIR26A1
MIR26A1 		microRNA 26a-1 0.653 0.577
CUI: C1565662
Disease: Acute Kidney Insufficiency
Acute Kidney Insufficiency 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 407015
Gene Symbol: MIR26A1
MIR26A1 		microRNA 26a-1 0.653 0.577
CUI: C2609414
Disease: Acute kidney injury
Acute kidney injury 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 55486
Gene Symbol: PARL
PARL 		presenilin associated rhomboid like 0.729 0.308 1.9E-04
CUI: C0023264
Disease: Leigh Disease
Leigh Disease 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 6016
Gene Symbol: RIT1
RIT1 		Ras like without CAAX 1 0.527 0.808 0.13
CUI: C0009207
Disease: Cockayne Syndrome
Cockayne Syndrome 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 6016
Gene Symbol: RIT1
RIT1 		Ras like without CAAX 1 0.527 0.808 0.13
CUI: C0032897
Disease: Prader-Willi Syndrome
Prader-Willi Syndrome 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 6016
Gene Symbol: RIT1
RIT1 		Ras like without CAAX 1 0.527 0.808 0.13
CUI: C0175691
Disease: Dubowitz syndrome
Dubowitz syndrome 		disease 0.200 None 1.000 1 0 2019 2019