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: 118856
Gene Symbol: MMP21
MMP21 		matrix metallopeptidase 21 0.621 0.385 1.3E-09
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		disease 0.200 None 0 0
Entrez Id: 118856
Gene Symbol: MMP21
MMP21 		matrix metallopeptidase 21 0.621 0.385 1.3E-09
CUI: C3151867
Disease: CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED 		disease 0.200 None 0 0
Entrez Id: 118856
Gene Symbol: MMP21
MMP21 		matrix metallopeptidase 21 0.621 0.385 1.3E-09
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		disease 0.200 None 0 0
Entrez Id: 119032
Gene Symbol: BORCS7
BORCS7 		BLOC-1 related complex subunit 7 0.890 0.115 2.3E-07
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		disease 0.200 None 0 0
Entrez Id: 119032
Gene Symbol: BORCS7
BORCS7 		BLOC-1 related complex subunit 7 0.890 0.115 2.3E-07
CUI: C0338473
Disease: Neuroaxonal Dystrophies
Neuroaxonal Dystrophies 		group 0.200 None 0 0
Entrez Id: 121536
Gene Symbol: AEBP2
AEBP2 		AE binding protein 2 0.821 0.192 1.00
CUI: C0079661
Disease: Klein's Syndrome
Klein's Syndrome 		disease 0.200 None 0 0
Entrez Id: 121536
Gene Symbol: AEBP2
AEBP2 		AE binding protein 2 0.821 0.192 1.00
CUI: C1847800
Disease: Waardenburg Syndrome Type 1
Waardenburg Syndrome Type 1 		disease 0.200 None 0 0
Entrez Id: 121536
Gene Symbol: AEBP2
AEBP2 		AE binding protein 2 0.821 0.192 1.00
CUI: C3266898
Disease: Waardenburg Syndrome
Waardenburg Syndrome 		disease 0.200 None 0 0
Entrez Id: 129401
Gene Symbol: NUP35
NUP35 		nucleoporin 35 0.890 0.192 2.2E-02
CUI: C0021847
Disease: Intestinal Pseudo-Obstruction
Intestinal Pseudo-Obstruction 		disease 0.200 None 0 0
Entrez Id: 1312
Gene Symbol: COMT
COMT 		catechol-O-methyltransferase 0.400 0.923 1.1E-06
CUI: C0029227
Disease: Delirium, Dementia, Amnestic, Cognitive Disorders
Delirium, Dementia, Amnestic, Cognitive Disorders 		group 0.200 None 0 0
Entrez Id: 131920
Gene Symbol: TMEM207
TMEM207 		transmembrane protein 207 0.792 0.231 4.2E-11
CUI: C0345988
Disease: Neoplasm of skin with adnexal differentiation
Neoplasm of skin with adnexal differentiation 		disease 0.200 None 0 0
Entrez Id: 1346
Gene Symbol: COX7A1
COX7A1 		cytochrome c oxidase subunit 7A1 0.805 0.192 3.7E-05
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		group 0.200 None 0 0
Entrez Id: 1352
Gene Symbol: COX10
COX10 		cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 0.623 0.654 8.4E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		disease 0.200 None 0 0
Entrez Id: 1352
Gene Symbol: COX10
COX10 		cytochrome c oxidase assembly factor heme A:farnesyltransferase COX10 0.623 0.654 8.4E-02
CUI: C0162670
Disease: Mitochondrial Myopathies
Mitochondrial Myopathies 		group 0.200 None 0 0
Entrez Id: 136319
Gene Symbol: MTPN
MTPN 		myotrophin 0.729 0.346 0.82
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		disease 0.200 None 0 0
Entrez Id: 136319
Gene Symbol: MTPN
MTPN 		myotrophin 0.729 0.346 0.82
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
Cardiomyopathy, Hypertrophic, Familial 		disease 0.200 None 0 0
Entrez Id: 1386
Gene Symbol: ATF2
ATF2 		activating transcription factor 2 0.551 0.808 0.99
CUI: C0008449
Disease: Congenital anomaly of cartilage
Congenital anomaly of cartilage 		group 0.200 None 0 0
Entrez Id: 1386
Gene Symbol: ATF2
ATF2 		activating transcription factor 2 0.551 0.808 0.99
CUI: C0029422
Disease: Osteochondrodysplasias
Osteochondrodysplasias 		group 0.200 None 0 0
Entrez Id: 1411
Gene Symbol: CRYBA1
CRYBA1 		crystallin beta A1 0.716 0.269 6.4E-05
CUI: C1864205
Disease: Macular Degeneration, Age-Related, 1
Macular Degeneration, Age-Related, 1 		disease 0.200 None 0 0
Entrez Id: 144165
Gene Symbol: PRICKLE1
PRICKLE1 		prickle planar cell polarity protein 1 0.647 0.615 1.00
CUI: C0220704
Disease: Shprintzen syndrome
Shprintzen syndrome 		disease 0.200 None 0 0
Entrez Id: 1453
Gene Symbol: CSNK1D
CSNK1D 		casein kinase 1 delta 0.650 0.615 1.00
CUI: C0041671
Disease: Attention Deficit Disorder
Attention Deficit Disorder 		disease 0.200 None 0 0
Entrez Id: 148345
Gene Symbol: C1orf127
C1orf127 		chromosome 1 open reading frame 127 0.729 0.308 1.5E-11
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		group 0.200 None 0 0
Entrez Id: 148345
Gene Symbol: C1orf127
C1orf127 		chromosome 1 open reading frame 127 0.729 0.308 1.5E-11
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		disease 0.200 None 0 0
Entrez Id: 148345
Gene Symbol: C1orf127
C1orf127 		chromosome 1 open reading frame 127 0.729 0.308 1.5E-11
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		disease 0.200 None 0 0
Entrez Id: 148345
Gene Symbol: C1orf127
C1orf127 		chromosome 1 open reading frame 127 0.729 0.308 1.5E-11
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		disease 0.200 None 0 0