Source: CLINVAR

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: C1848673
Disease: Hypoplastic feet
Hypoplastic feet 		phenotype 0.100 None 0 1
Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24 		zinc metallopeptidase STE24 0.517 0.731 8.9E-16
CUI: C1849075
Disease: Relative macrocephaly
Relative macrocephaly 		disease 0.100 None 0 1
Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24 		zinc metallopeptidase STE24 0.517 0.731 8.9E-16
CUI: C1855650
Disease: Birth length less than 3rd percentile
Birth length less than 3rd percentile 		phenotype 0.100 None 0 1
Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24 		zinc metallopeptidase STE24 0.517 0.731 8.9E-16
CUI: C1857042
Disease: Sparse scalp hair
Sparse scalp hair 		phenotype 0.100 None 0 1
Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24 		zinc metallopeptidase STE24 0.517 0.731 8.9E-16
CUI: C1857790
Disease: Thoracic scoliosis
Thoracic scoliosis 		phenotype 0.100 None 0 1
Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24 		zinc metallopeptidase STE24 0.517 0.731 8.9E-16
CUI: C2677180
Disease: Congenital microcephaly
Congenital microcephaly 		disease 0.100 None 0 1
Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24 		zinc metallopeptidase STE24 0.517 0.731 8.9E-16
CUI: C3278923
Disease: Dilated ventricles (finding)
Dilated ventricles (finding) 		phenotype 0.100 None 0 1
Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24 		zinc metallopeptidase STE24 0.517 0.731 8.9E-16
CUI: C4021829
Disease: Narrow nail
Narrow nail 		phenotype 0.100 None 0 1
Entrez Id: 10269
Gene Symbol: ZMPSTE24
ZMPSTE24 		zinc metallopeptidase STE24 0.517 0.731 8.9E-16
CUI: C4281993
Disease: Neonatal respiratory distress
Neonatal respiratory distress 		phenotype 0.100 None 0 1
Entrez Id: 57688
Gene Symbol: ZSWIM6
ZSWIM6 		zinc finger SWIM-type containing 6 0.626 0.577 1.00
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		group 0.100 None 1.000 3 1 2014 2017
Entrez Id: 57688
Gene Symbol: ZSWIM6
ZSWIM6 		zinc finger SWIM-type containing 6 0.626 0.577 1.00
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		phenotype 0.100 None 1.000 3 1 2014 2017
Entrez Id: 57688
Gene Symbol: ZSWIM6
ZSWIM6 		zinc finger SWIM-type containing 6 0.626 0.577 1.00
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		disease 0.100 None 1.000 3 1 2014 2017
Entrez Id: 57688
Gene Symbol: ZSWIM6
ZSWIM6 		zinc finger SWIM-type containing 6 0.626 0.577 1.00
CUI: C1863616
Disease: ACROMELIC FRONTONASAL DYSOSTOSIS
ACROMELIC FRONTONASAL DYSOSTOSIS 		disease 0.740 None 1.000 2 1 2014 2017
Entrez Id: 57688
Gene Symbol: ZSWIM6
ZSWIM6 		zinc finger SWIM-type containing 6 0.626 0.577 1.00
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability 		disease 0.120 None 1.000 1 1 2017 2017
Entrez Id: 57688
Gene Symbol: ZSWIM6
ZSWIM6 		zinc finger SWIM-type containing 6 0.626 0.577 1.00
CUI: C4693405
Disease: NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES
NEURODEVELOPMENTAL DISORDER WITH MOVEMENT ABNORMALITIES, ABNORMAL GAIT, AND AUTISTIC FEATURES 		disease 0.400 strong 1.000 0 1 2014 2014
Entrez Id: 84083
Gene Symbol: ZRANB3
ZRANB3 		zinc finger RANBP2-type containing 3 0.780 0.577 4.2E-21
CUI: C0009691
Disease: Congenital cataract
Congenital cataract 		disease 0.100 None 0 1
Entrez Id: 84083
Gene Symbol: ZRANB3
ZRANB3 		zinc finger RANBP2-type containing 3 0.780 0.577 4.2E-21
CUI: C0266544
Disease: Microcornea
Microcornea 		disease 0.100 None 0 1
Entrez Id: 84083
Gene Symbol: ZRANB3
ZRANB3 		zinc finger RANBP2-type containing 3 0.780 0.577 4.2E-21
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		disease 0.100 None 0 1
Entrez Id: 84083
Gene Symbol: ZRANB3
ZRANB3 		zinc finger RANBP2-type containing 3 0.780 0.577 4.2E-21
CUI: C0423224
Disease: Sunken eyes
Sunken eyes 		phenotype 0.100 None 0 1
Entrez Id: 84083
Gene Symbol: ZRANB3
ZRANB3 		zinc finger RANBP2-type containing 3 0.780 0.577 4.2E-21
CUI: C1838625
Disease: Warburg Sjo Fledelius syndrome
Warburg Sjo Fledelius syndrome 		disease 0.110 None < 0.001 0 6 2013 2013
Entrez Id: 23414
Gene Symbol: ZFPM2
ZFPM2 		zinc finger protein, FOG family member 2 0.565 0.731 1.00
CUI: C0013069
Disease: Double Outlet Right Ventricle
Double Outlet Right Ventricle 		disease 0.130 None 1.000 0 2 2011 2014
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 0 1 2000 2018
Entrez Id: 23414
Gene Symbol: ZFPM2
ZFPM2 		zinc finger protein, FOG family member 2 0.565 0.731 1.00
CUI: C1857781
Disease: Diaphragmatic Hernia 3
Diaphragmatic Hernia 3 		disease 0.600 limited 1.000 0 2 2005 2005
Entrez Id: 23414
Gene Symbol: ZFPM2
ZFPM2 		zinc finger protein, FOG family member 2 0.565 0.731 1.00
CUI: C4015129
Disease: 46,XY SEX REVERSAL 9
46,XY SEX REVERSAL 9 		disease 0.700 moderate 1.000 0 3 2014 2015
Entrez Id: 7552
Gene Symbol: ZNF711
ZNF711 		zinc finger protein 711 0.691 0.423 0.98
CUI: C0026351
Disease: Moderate intellectual disability
Moderate intellectual disability 		disease 0.100 None 1.000 2 1 2009 2017