Source: ALL

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: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		disease 0.300 None 1.000 1 0 2015 2015
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C0025958
Disease: Microcephaly
Microcephaly 		disease 0.110 None 1.000 1 0 2013 2013
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		disease 0.100 None 0.975 81 0 1995 2020
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary 		disease 0.100 None 1.000 15 0 1996 2019
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C0206526
Disease: Tuberculosis, Multidrug-Resistant
Tuberculosis, Multidrug-Resistant 		disease 0.100 None 1.000 11 0 1999 2018
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C0042580
Disease: Vesico-Ureteral Reflux
Vesico-Ureteral Reflux 		disease 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C0333068
Disease: Flexion contracture
Flexion contracture 		disease 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C0266295
Disease: Congenital hypoplasia of kidney
Congenital hypoplasia of kidney 		disease 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C0265610
Disease: Clinodactyly of fingers
Clinodactyly of fingers 		disease 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C0241726
Disease: Delayed ability to walk
Delayed ability to walk 		phenotype 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		phenotype 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C0221354
Disease: Frontal bossing
Frontal bossing 		disease 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL 		disease 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C0344503
Disease: Congenital epiblepharon
Congenital epiblepharon 		disease 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C0344559
Disease: Irido-corneo-trabecular dysgenesis (disorder)
Irido-corneo-trabecular dysgenesis (disorder) 		disease 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C0349588
Disease: Short stature
Short stature 		phenotype 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C0349702
Disease: Corneal Scar
Corneal Scar 		phenotype 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C3665347
Disease: Visual Impairment
Visual Impairment 		phenotype 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C2919142
Disease: Short Stature, CTCAE
Short Stature, CTCAE 		phenotype 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0 		phenotype 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		phenotype 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C1854882
Disease: Absent speech
Absent speech 		phenotype 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C1849341
Disease: Triangular mouth
Triangular mouth 		phenotype 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C1840379
Disease: Cerebellar vermis hypoplasia
Cerebellar vermis hypoplasia 		phenotype 0.100 None 0 0
Entrez Id: 54892
Gene Symbol: NCAPG2
NCAPG2 		non-SMC condensin II complex subunit G2 0.603 0.731 0.98
CUI: C1839767
Disease: Tented upper lip vermilion
Tented upper lip vermilion 		phenotype 0.100 None 0 0