Source: INFERRED

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: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C4225412
Disease: Spondylo-ocular syndrome
Spondylo-ocular syndrome 		disease 0.450 None 1.000 0 3 2015 2019
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		disease 0.110 None 1.000 0 0 2006 2006
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		group 0.100 None 1.000 4 1 2015 2018
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		disease 0.100 None 1.000 4 1 2015 2018
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C1837732
Disease: Thickened helices
Thickened helices 		phenotype 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C1842774
Disease: Hypermelanotic macule
Hypermelanotic macule 		phenotype 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C1844704
Disease: Platyspondyly
Platyspondyly 		phenotype 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C1845251
Disease: Facial hypotonia
Facial hypotonia 		phenotype 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C1846435
Disease: Disproportionate short-trunk short stature
Disproportionate short-trunk short stature 		phenotype 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C1834124
Disease: Shield chest
Shield chest 		phenotype 0.100 None 0 1
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C1565489
Disease: Renal Insufficiency
Renal Insufficiency 		disease 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C1260959
Disease: Drusen
Drusen 		disease 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C1184919
Disease: Thoracic kyphosis
Thoracic kyphosis 		phenotype 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C0600518
Disease: Choroidal Neovascularization
Choroidal Neovascularization 		phenotype 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C0578038
Disease: Thin lips
Thin lips 		phenotype 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C0521525
Disease: Short neck
Short neck 		phenotype 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C0431478
Disease: Posteriorly rotated ear
Posteriorly rotated ear 		disease 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C1849618
Disease: Accelerated atherosclerosis
Accelerated atherosclerosis 		phenotype 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C1855728
Disease: Low posterior hairline
Low posterior hairline 		phenotype 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0 		phenotype 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C4025249
Disease: Abnormality of the intervertebral disk
Abnormality of the intervertebral disk 		disease 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C4024738
Disease: Aplasia/Hypoplasia of the lens
Aplasia/Hypoplasia of the lens 		phenotype 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C4021395
Disease: Abnormality of the antihelix
Abnormality of the antihelix 		disease 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C4011556
Disease: Abnormal eyebrow morphology
Abnormal eyebrow morphology 		group 0.100 None 0 0
Entrez Id: 64132
Gene Symbol: XYLT2
XYLT2 		xylosyltransferase 2 0.566 0.808 0.93
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		group 0.100 None 0 0