Source: MGD

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: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24 		zinc metallopeptidase STE24 0.517 0.731 8.9E-16
CUI: C0033300
Disease: Progeria
Progeria 		disease 0.800 None 0.967 5 0 2002 2019
Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24 		zinc metallopeptidase STE24 0.517 0.731 8.9E-16
CUI: C0271694
Disease: Familial partial lipodystrophy
Familial partial lipodystrophy 		disease 0.210 None 1.000 0 0 2007 2007
Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24 		zinc metallopeptidase STE24 0.517 0.731 8.9E-16
CUI: C0410189
Disease: Muscular Dystrophy, Emery-Dreifuss
Muscular Dystrophy, Emery-Dreifuss 		disease 0.200 None 0 0
Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24 		zinc metallopeptidase STE24 0.517 0.731 8.9E-16
CUI: C1720859
Disease: Familial Partial Lipodystrophy, Type 1
Familial Partial Lipodystrophy, Type 1 		disease 0.200 None 0 0
Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24 		zinc metallopeptidase STE24 0.517 0.731 8.9E-16
CUI: C1720860
Disease: Familial Partial Lipodystrophy, Type 2
Familial Partial Lipodystrophy, Type 2 		disease 0.200 None 0 0
Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24 		zinc metallopeptidase STE24 0.517 0.731 8.9E-16
CUI: C1720861
Disease: Familial Partial Lipodystrophy, Type 3
Familial Partial Lipodystrophy, Type 3 		disease 0.200 None 0 0
Entrez Id: 23414
Gene Symbol: ZFPM2
ZFPM2 		zinc finger protein, FOG family member 2 0.565 0.731 1.00
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		disease 1.000 limited 0.929 2 0 2000 2018
Entrez Id: 23414
Gene Symbol: ZFPM2
ZFPM2 		zinc finger protein, FOG family member 2 0.565 0.731 1.00
CUI: C0019284
Disease: Diaphragmatic Hernia
Diaphragmatic Hernia 		phenotype 0.510 None 1.000 1 0 2005 2007
Entrez Id: 23414
Gene Symbol: ZFPM2
ZFPM2 		zinc finger protein, FOG family member 2 0.565 0.731 1.00
CUI: C0243002
Disease: Tricuspid Atresia
Tricuspid Atresia 		disease 0.210 None 1.000 1 0 2000 2005
Entrez Id: 25925
Gene Symbol: ZNF521
ZNF521 		zinc finger protein 521 0.700 0.385 1.00
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		disease 0.200 None 1.000 1 0 2014 2014
Entrez Id: 58499
Gene Symbol: ZNF462
ZNF462 		zinc finger protein 462 0.711 0.462 1.00
CUI: C0270549
Disease: Generalized Anxiety Disorder
Generalized Anxiety Disorder 		disease 0.200 None 0 0
Entrez Id: 23090
Gene Symbol: ZNF423
ZNF423 		zinc finger protein 423 0.592 0.808 1.00
CUI: C0010964
Disease: Dandy-Walker Syndrome
Dandy-Walker Syndrome 		disease 0.200 None 1.000 1 0 2006 2006
Entrez Id: 23090
Gene Symbol: ZNF423
ZNF423 		zinc finger protein 423 0.592 0.808 1.00
CUI: C0007760
Disease: Cerebellar Diseases
Cerebellar Diseases 		group 0.200 None 0 0
Entrez Id: 167465
Gene Symbol: ZNF366
ZNF366 		zinc finger protein 366 0.729 0.423 7.0E-02
CUI: C0012236
Disease: DiGeorge Syndrome
DiGeorge Syndrome 		disease 0.200 None 0 0
Entrez Id: 64397
Gene Symbol: ZNF106
ZNF106 		zinc finger protein 106 0.890 0.154 1.1E-04
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		disease 0.210 None 1.000 1 0 2017 2017
Entrez Id: 51364
Gene Symbol: ZMYND10
ZMYND10 		zinc finger MYND-type containing 10 0.553 0.731 2.3E-07
CUI: C0265747
Disease: Congenital atresia of nasopharynx
Congenital atresia of nasopharynx 		disease 0.200 None 1.000 1 0 2018 2018
Entrez Id: 51364
Gene Symbol: ZMYND10
ZMYND10 		zinc finger MYND-type containing 10 0.553 0.731 2.3E-07
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 2018 2018
Entrez Id: 51364
Gene Symbol: ZMYND10
ZMYND10 		zinc finger MYND-type containing 10 0.553 0.731 2.3E-07
CUI: C3809543
Disease: CILIARY DYSKINESIA, PRIMARY, 22
CILIARY DYSKINESIA, PRIMARY, 22 		disease 0.900 None 1.000 1 0 2013 2018
Entrez Id: 23503
Gene Symbol: ZFYVE26
ZFYVE26 		zinc finger FYVE-type containing 26 0.636 0.615 4.7E-23
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		disease 0.390 None 1.000 1 0 2007 2019
Entrez Id: 23503
Gene Symbol: ZFYVE26
ZFYVE26 		zinc finger FYVE-type containing 26 0.636 0.615 4.7E-23
CUI: C1849128
Disease: Spastic paraplegia 15, autosomal recessive
Spastic paraplegia 15, autosomal recessive 		disease 0.950 None 1.000 1 0 2007 2016
Entrez Id: 9839
Gene Symbol: ZEB2
ZEB2 		zinc finger E-box binding homeobox 2 0.471 0.808 1.00
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome 		disease 1.000 definitive 1.000 1 0 1991 2019
Entrez Id: 9839
Gene Symbol: ZEB2
ZEB2 		zinc finger E-box binding homeobox 2 0.471 0.808 1.00
CUI: C0279592
Disease: Adult T Acute Lymphoblastic Leukemia
Adult T Acute Lymphoblastic Leukemia 		disease 0.200 None 0 0
Entrez Id: 6935
Gene Symbol: ZEB1
ZEB1 		zinc finger E-box binding homeobox 1 0.442 0.808 0.97
CUI: C0030481
Disease: Tropical Spastic Paraparesis
Tropical Spastic Paraparesis 		disease 0.200 None 1.000 1 0 2008 2008
Entrez Id: 51114
Gene Symbol: ZDHHC9
ZDHHC9 		zinc finger DHHC-type palmitoyltransferase 9 0.670 0.577 0.74
CUI: C0869083
Disease: Other specified congenital malformation syndromes, not elsewhere classified in ICD10CM
Other specified congenital malformation syndromes, not elsewhere classified in ICD10CM 		disease 0.200 None 1.000 1 0 2018 2018
Entrez Id: 51114
Gene Symbol: ZDHHC9
ZDHHC9 		zinc finger DHHC-type palmitoyltransferase 9 0.670 0.577 0.74
CUI: C3275406
Disease: MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE
MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE 		disease 0.900 strong 1.000 1 0 2007 2018