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: 8989
Gene Symbol: TRPA1
TRPA1 		transient receptor potential cation channel subfamily A member 1 0.546 0.846 7.2E-35
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		phenotype 0.200 None 1.000 1 0 2014 2014
Entrez Id: 2353
Gene Symbol: FOS
FOS 		Fos proto-oncogene, AP-1 transcription factor subunit 0.411 0.885 0.26
CUI: C1879526
Disease: Aberrant Crypt Foci
Aberrant Crypt Foci 		phenotype 0.200 None 1.000 2 0 1992 1993
Entrez Id: 2932
Gene Symbol: GSK3B
GSK3B 		glycogen synthase kinase 3 beta 0.430 0.846 0.96
CUI: C1879526
Disease: Aberrant Crypt Foci
Aberrant Crypt Foci 		phenotype 0.200 None 1.000 1 0 2014 2014
Entrez Id: 4609
Gene Symbol: MYC
MYC 		MYC proto-oncogene, bHLH transcription factor 0.344 0.923 1.00
CUI: C1879526
Disease: Aberrant Crypt Foci
Aberrant Crypt Foci 		phenotype 0.200 None 1.000 1 0 1993 1993
Entrez Id: 7042
Gene Symbol: TGFB2
TGFB2 		transforming growth factor beta 2 0.433 0.885 1.00
CUI: C1879526
Disease: Aberrant Crypt Foci
Aberrant Crypt Foci 		phenotype 0.200 None 1.000 1 0 2006 2006
Entrez Id: 57152
Gene Symbol: SLURP1
SLURP1 		secreted LY6/PLAUR domain containing 1 0.560 0.654 0.26
CUI: C0432333
Disease: Abnormal dermatoglyphic pattern
Abnormal dermatoglyphic pattern 		disease 0.200 None 1.000 1 0 2014 2014
Entrez Id: 57152
Gene Symbol: SLURP1
SLURP1 		secreted LY6/PLAUR domain containing 1 0.560 0.654 0.26
CUI: C0221199
Disease: Abnormal palmar creases
Abnormal palmar creases 		disease 0.200 None 1.000 1 0 2014 2014
Entrez Id: 866
Gene Symbol: SERPINA6
SERPINA6 		serpin family A member 6 0.606 0.731 8.3E-07
CUI: C0271749
Disease: Abnormality of cortisol-binding globulin
Abnormality of cortisol-binding globulin 		disease 0.200 None 1.000 2 0 2006 2010
Entrez Id: 10369
Gene Symbol: CACNG2
CACNG2 		calcium voltage-gated channel auxiliary subunit gamma 2 0.729 0.385 0.92
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		disease 0.200 None 1.000 1 0 2008 2008
Entrez Id: 2746
Gene Symbol: GLUD1
GLUD1 		glutamate dehydrogenase 1 0.584 0.731 7.0E-03
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		disease 0.200 None 1.000 1 0 2000 2000
Entrez Id: 3363
Gene Symbol: HTR7
HTR7 		5-hydroxytryptamine receptor 7 0.592 0.500 4.5E-02
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		disease 0.200 None 1.000 1 0 2004 2004
Entrez Id: 348980
Gene Symbol: HCN1
HCN1 		hyperpolarization activated cyclic nucleotide gated potassium channel 1 0.564 0.654 1.00
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		disease 0.230 None 1.000 1 0 2004 2020
Entrez Id: 4318
Gene Symbol: MMP9
MMP9 		matrix metallopeptidase 9 0.305 0.923 1.9E-17
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		disease 0.200 None 1.000 1 0 2010 2010
Entrez Id: 4852
Gene Symbol: NPY
NPY 		neuropeptide Y 0.447 0.846 0.14
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		disease 0.220 None 1.000 1 0 2013 2018
Entrez Id: 4886
Gene Symbol: NPY1R
NPY1R 		neuropeptide Y receptor Y1 0.628 0.423 4.3E-02
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		disease 0.200 None 1.000 1 0 2007 2007
Entrez Id: 4887
Gene Symbol: NPY2R
NPY2R 		neuropeptide Y receptor Y2 0.612 0.577 3.6E-02
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		disease 0.200 None 1.000 1 0 2007 2007
Entrez Id: 4889
Gene Symbol: NPY5R
NPY5R 		neuropeptide Y receptor Y5 0.691 0.462 6.4E-03
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		disease 0.200 None 1.000 1 0 2007 2007
Entrez Id: 7534
Gene Symbol: YWHAZ
YWHAZ 		tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta 0.475 0.846 0.94
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		disease 0.200 None 1.000 1 0 2011 2011
Entrez Id: 773
Gene Symbol: CACNA1A
CACNA1A 		calcium voltage-gated channel subunit alpha1 A 0.489 0.769 1.00
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		disease 0.760 strong 1.000 1 0 1996 2020
Entrez Id: 5243
Gene Symbol: ABCB1
ABCB1 		ATP binding cassette subfamily B member 1 0.344 0.885 1.3E-05
CUI: C4316903
Disease: Absence Seizures
Absence Seizures 		phenotype 0.200 None 1.000 1 0 2007 2007
Entrez Id: 6662
Gene Symbol: SOX9
SOX9 		SRY-box transcription factor 9 0.419 0.846 1.00
CUI: C1861923
Disease: Acampomelic Campomelic Dysplasia
Acampomelic Campomelic Dysplasia 		disease 0.690 None 1.000 3 0 2000 2018
Entrez Id: 7099
Gene Symbol: TLR4
TLR4 		toll like receptor 4 0.321 0.962 4.6E-09
CUI: C0000880
Disease: Acanthamoeba Keratitis
Acanthamoeba Keratitis 		disease 0.220 None 1.000 1 0 2011 2016
Entrez Id: 5243
Gene Symbol: ABCB1
ABCB1 		ATP binding cassette subfamily B member 1 0.344 0.885 1.3E-05
CUI: C0234238
Disease: Ache
Ache 		phenotype 0.200 None 1.000 1 0 2017 2017
Entrez Id: 64327
Gene Symbol: LMBR1
LMBR1 		limb development membrane protein 1 0.619 0.308 1.3E-08
CUI: C0265559
Disease: Acheiropodia
Acheiropodia 		disease 0.820 strong 1.000 1 0 2001 2016
Entrez Id: 3784
Gene Symbol: KCNQ1
KCNQ1 		potassium voltage-gated channel subfamily Q member 1 0.485 0.769 4.5E-08
CUI: C0001075
Disease: Achlorhydria
Achlorhydria 		phenotype 0.200 None 1.000 1 0 2006 2006