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: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C3150731
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 		disease 0.610 None 1.000 0 6 2010 2018
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C0037769
Disease: West Syndrome
West Syndrome 		disease 0.460 None 1.000 0 0 2008 2017
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy 		disease 0.140 None 1.000 0 0 2012 2017
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		disease 0.130 None 1.000 0 1 2015 2018
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C0036572
Disease: Seizures
Seizures 		phenotype 0.120 None 1.000 2 1 2012 2017
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability 		disease 0.110 None 1.000 0 0 2015 2015
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C4552072
Disease: X-linked infantile spasms
X-linked infantile spasms 		disease 0.110 None 1.000 0 1 2012 2012
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		disease 0.100 None 1.000 1 5 2018 2018
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C1861403
Disease: Variable expressivity
Variable expressivity 		phenotype 0.100 None 0 0
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities 		disease 0.100 None 0 0
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		phenotype 0.100 None 0 1
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C4023528
Disease: Abnormality of skin morphology
Abnormality of skin morphology 		phenotype 0.100 None 0 0
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C4024900
Disease: Atrophy/Degeneration affecting the brainstem
Atrophy/Degeneration affecting the brainstem 		disease 0.100 None 0 0
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C4025616
Disease: CNS hypomyelination
CNS hypomyelination 		phenotype 0.100 None 0 0
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		phenotype 0.100 None 0 0
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C1850456
Disease: Progressive microcephaly
Progressive microcephaly 		phenotype 0.100 None 0 0
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C1836830
Disease: Developmental regression
Developmental regression 		disease 0.100 None 0 0
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		disease 0.100 None 0 0
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia 		phenotype 0.100 None 0 0
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C0426970
Disease: Spastic Quadriplegia
Spastic Quadriplegia 		disease 0.100 None 0 0
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		disease 0.100 None 0 0
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C0151889
Disease: Hyperreflexia
Hyperreflexia 		phenotype 0.100 None 0 0
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C0027066
Disease: Myoclonus
Myoclonus 		phenotype 0.100 None 0 0
Entrez Id: 6709
Gene Symbol: SPTAN1
SPTAN1 		spectrin alpha, non-erythrocytic 1 0.601 0.615 1.00
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial 		disease 0.100 None 0 1