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: 148345
Gene Symbol: C1orf127
C1orf127 		chromosome 1 open reading frame 127 0.729 0.308 1.5E-11
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, 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: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, 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: 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: 148345
Gene Symbol: C1orf127
C1orf127 		chromosome 1 open reading frame 127 0.729 0.308 1.5E-11
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy 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: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		disease 0.200 None 0 0
Entrez Id: 1489
Gene Symbol: CTF1
CTF1 		cardiotrophin 1 0.636 0.423 4.2E-02
CUI: C2930930
Disease: Abdominal obesity metabolic syndrome
Abdominal obesity metabolic syndrome 		disease 0.200 None 0 0
Entrez Id: 149041
Gene Symbol: RC3H1
RC3H1 		ring finger and CCCH-type domains 1 0.821 0.154 0.99
CUI: C0079774
Disease: Peripheral T-Cell Lymphoma
Peripheral T-Cell Lymphoma 		disease 0.200 None 0 0
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1 		catenin beta 1 0.303 0.885 1.00
CUI: C0334401
Disease: Malignant Granulosa Cell Tumor
Malignant Granulosa Cell Tumor 		disease 0.200 None 0 0
Entrez Id: 1499
Gene Symbol: CTNNB1
CTNNB1 		catenin beta 1 0.303 0.885 1.00
CUI: C1299247
Disease: Primary malignant neoplasm of ovary and other uterine adnexa
Primary malignant neoplasm of ovary and other uterine adnexa 		disease 0.200 None 0 0
Entrez Id: 1515
Gene Symbol: CTSV
CTSV 		cathepsin V 0.716 0.462 2.3E-07
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		group 0.200 None 0 0
Entrez Id: 1520
Gene Symbol: CTSS
CTSS 		cathepsin S 0.539 0.731 0.34
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne 		disease 0.200 None 0 0
Entrez Id: 157657
Gene Symbol: C8orf37
C8orf37 		chromosome 8 open reading frame 37 0.628 0.538 2.4E-05
CUI: C0220701
Disease: RETINITIS PIGMENTOSA 1
RETINITIS PIGMENTOSA 1 		disease 0.200 None 0 0
Entrez Id: 1588
Gene Symbol: CYP19A1
CYP19A1 		cytochrome P450 family 19 subfamily A member 1 0.410 0.885 1.7E-05
CUI: C0342548
Disease: Early menarche
Early menarche 		phenotype 0.200 None 0 0
Entrez Id: 1605
Gene Symbol: DAG1
DAG1 		dystroglycan 1 0.498 0.808 0.98
CUI: C0266483
Disease: Pachygyria
Pachygyria 		disease 0.300 None 0 0
Entrez Id: 161582
Gene Symbol: DNAAF4
DNAAF4 		dynein axonemal assembly factor 4 0.623 0.731 9.7E-10
CUI: C0265205
Disease: Robinow Syndrome
Robinow Syndrome 		disease 0.200 None 0 0
Entrez Id: 162
Gene Symbol: AP1B1
AP1B1 		adaptor related protein complex 1 subunit beta 1 0.716 0.385 1.00
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		group 0.200 None 0 0
Entrez Id: 162
Gene Symbol: AP1B1
AP1B1 		adaptor related protein complex 1 subunit beta 1 0.716 0.385 1.00
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		disease 0.200 None 0 0
Entrez Id: 162
Gene Symbol: AP1B1
AP1B1 		adaptor related protein complex 1 subunit beta 1 0.716 0.385 1.00
CUI: C1415817
Disease: HETEROTAXY, VISCERAL, 2, AUTOSOMAL
HETEROTAXY, VISCERAL, 2, AUTOSOMAL 		disease 0.200 None 0 0
Entrez Id: 162
Gene Symbol: AP1B1
AP1B1 		adaptor related protein complex 1 subunit beta 1 0.716 0.385 1.00
CUI: C1844020
Disease: HETEROTAXY, VISCERAL, 1, X-LINKED
HETEROTAXY, VISCERAL, 1, X-LINKED 		disease 0.200 None 0 0
Entrez Id: 162
Gene Symbol: AP1B1
AP1B1 		adaptor related protein complex 1 subunit beta 1 0.716 0.385 1.00
CUI: C1853444
Disease: Heterotaxy, Visceral, 3, Autosomal
Heterotaxy, Visceral, 3, Autosomal 		disease 0.200 None 0 0
Entrez Id: 162
Gene Symbol: AP1B1
AP1B1 		adaptor related protein complex 1 subunit beta 1 0.716 0.385 1.00
CUI: C3151057
Disease: HETEROTAXY, VISCERAL, 4, AUTOSOMAL
HETEROTAXY, VISCERAL, 4, AUTOSOMAL 		disease 0.200 None 0 0
Entrez Id: 162
Gene Symbol: AP1B1
AP1B1 		adaptor related protein complex 1 subunit beta 1 0.716 0.385 1.00
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: 162
Gene Symbol: AP1B1
AP1B1 		adaptor related protein complex 1 subunit beta 1 0.716 0.385 1.00
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		disease 0.200 None 0 0
Entrez Id: 162
Gene Symbol: AP1B1
AP1B1 		adaptor related protein complex 1 subunit beta 1 0.716 0.385 1.00
CUI: C3553676
Disease: HETEROTAXY, VISCERAL, 6, AUTOSOMAL
HETEROTAXY, VISCERAL, 6, AUTOSOMAL 		disease 0.200 None 0 0
Entrez Id: 165904
Gene Symbol: XIRP1
XIRP1 		xin actin binding repeat containing 1 0.780 0.269 2.3E-30
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		disease 0.200 None 0 0