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: 6016
Gene Symbol: RIT1
RIT1 		Ras like without CAAX 1 0.527 0.808 0.13
CUI: C0175693
Disease: Russell-Silver syndrome
Russell-Silver 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: C0175701
Disease: Aarskog syndrome
Aarskog 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: C0265202
Disease: Seckel syndrome
Seckel 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: C0265205
Disease: Robinow Syndrome
Robinow 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: C0270972
Disease: Cornelia De Lange Syndrome
Cornelia De Lange 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: C0347915
Disease: Congenital malformation syndromes associated with short stature
Congenital malformation syndromes associated with short stature 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 6352
Gene Symbol: CCL5
CCL5 		C-C motif chemokine ligand 5 0.403 0.885 1.8E-03
CUI: C0001306
Disease: Acute alcoholic liver disease
Acute alcoholic liver disease 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 6548
Gene Symbol: SLC9A1
SLC9A1 		solute carrier family 9 member A1 0.550 0.731 0.79
CUI: C0033687
Disease: Proteinuria
Proteinuria 		phenotype 0.200 None 1.000 1 0 2019 2019
Entrez Id: 6548
Gene Symbol: SLC9A1
SLC9A1 		solute carrier family 9 member A1 0.550 0.731 0.79
CUI: C0740392
Disease: Infarction, Middle Cerebral Artery
Infarction, Middle Cerebral Artery 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 7040
Gene Symbol: TGFB1
TGFB1 		transforming growth factor beta 1 0.287 0.962 3.7E-02
CUI: C0002103
Disease: Atopic rhinitis
Atopic rhinitis 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 841
Gene Symbol: CASP8
CASP8 		caspase 8 0.404 0.923 3.7E-06
CUI: C0007787
Disease: Transient Ischemic Attack
Transient Ischemic Attack 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 84329
Gene Symbol: HVCN1
HVCN1 		hydrogen voltage gated channel 1 0.751 0.346 0.63
CUI: C0740392
Disease: Infarction, Middle Cerebral Artery
Infarction, Middle Cerebral Artery 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 90956
Gene Symbol: ADCK2
ADCK2 		aarF domain containing kinase 2 3.6E-07
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies 		group 0.200 None 1.000 1 0 2019 2019
Entrez Id: 9211
Gene Symbol: LGI1
LGI1 		leucine rich glioma inactivated 1 0.568 0.731 1.00
CUI: C0014549
Disease: Tonic-Clonic Epilepsy
Tonic-Clonic Epilepsy 		disease 0.200 None 1.000 1 0 2019 2019
Entrez Id: 10486
Gene Symbol: CAP2
CAP2 		cyclase associated actin cytoskeleton regulatory protein 2 0.716 0.423 0.70
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		group 0.320 None 1.000 0 0 2019 2019
Entrez Id: 116512
Gene Symbol: MRGPRD
MRGPRD 		MAS related GPR family member D 0.861 0.192
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		group 0.210 None 1.000 0 0 2019 2019
Entrez Id: 22839
Gene Symbol: DLGAP4
DLGAP4 		DLG associated protein 4 0.769 0.269 0.99
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders 		disease 0.210 None 1.000 0 0 2019 2019
Entrez Id: 2355
Gene Symbol: FOSL2
FOSL2 		FOS like 2, AP-1 transcription factor subunit 0.595 0.692 0.98
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis 		disease 0.210 None 1.000 0 0 2019 2019
Entrez Id: 23568
Gene Symbol: ARL2BP
ARL2BP 		ADP ribosylation factor like GTPase 2 binding protein 0.647 0.654 3.3E-05
CUI: C0021364
Disease: Male infertility
Male infertility 		phenotype 0.210 None 1.000 0 0 2019 2019
Entrez Id: 3635
Gene Symbol: INPP5D
INPP5D 		inositol polyphosphate-5-phosphatase D 0.558 0.731 0.97
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		disease 0.210 None 1.000 0 0 2019 2019
Entrez Id: 4854
Gene Symbol: NOTCH3
NOTCH3 		notch receptor 3 0.435 0.808 0.41
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		disease 0.210 None 1.000 0 0 2019 2019
Entrez Id: 5734
Gene Symbol: PTGER4
PTGER4 		prostaglandin E receptor 4 0.558 0.731 0.98
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		group 0.210 None 1.000 0 0 2019 2019
Entrez Id: 84071
Gene Symbol: ARMC2
ARMC2 		armadillo repeat containing 2 0.805 0.115 2.5E-09
CUI: C0021364
Disease: Male infertility
Male infertility 		phenotype 0.310 None 1.000 0 0 2019 2019
Entrez Id: 84957
Gene Symbol: RELT
RELT 		RELT TNF receptor 0.821 0.077 1.1E-06
CUI: C0002452
Disease: Amelogenesis Imperfecta
Amelogenesis Imperfecta 		disease 0.320 None 1.000 0 0 2019 2019
Entrez Id: 8701
Gene Symbol: DNAH11
DNAH11 		dynein axonemal heavy chain 11 0.587 0.692 2.5E-58
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		disease 0.210 None 1.000 0 0 2019 2019