| 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. | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
Chromosome 22q11.2 deletion syndrome, distal | 1.000 | 0.038 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2012 | 2012 | |||||||||
|
clavesin 2 | 1.000 | 0.038 | 1.4E-02 |
|
disease | 0.310 | None | 1.000 | 1 | 0 | 2014 | 2014 | ||||||||
|
solute carrier family 23 member 3 | 1.000 | 0.038 | 7.4E-07 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2013 | 2013 | ||||||||
|
ADNP homeobox 2 | 1.000 | 0.038 | 0.70 |
|
disease | 0.320 | None | 1.000 | 1 | 0 | 2011 | 2015 | ||||||||
|
F-box and leucine rich repeat protein 21, pseudogene | 1.000 | 0.038 |
|
disease | 0.310 | None | 1.000 | 1 | 0 | 2008 | 2008 | |||||||||
|
biogenesis of lysosomal organelles complex 1 subunit 1 | 1.000 | 0.038 | 7.1E-02 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2015 | 2015 | ||||||||
|
deafness, autosomal recessive 47 | 1.000 | 0.038 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2008 | 2008 | |||||||||
|
calcium voltage-gated channel auxiliary subunit gamma 8 | 1.000 | 0.038 | 0.96 |
|
disease | 0.320 | None | 1.000 | 1 | 0 | 2013 | 2016 | ||||||||
|
small nucleolar RNA, C/D box 103C | 1.000 | 0.038 |
|
disease | 0.310 | None | 1.000 | 1 | 0 | 2014 | 2014 | |||||||||
|
leucine rich repeat transmembrane neuronal 1 | 0.931 | 0.038 | 0.59 |
|
disease | 0.540 | None | 1.000 | 2 | 0 | 2007 | 2014 | ||||||||
|
beta-1,3-glucuronyltransferase 2 | 0.931 | 0.115 | 3.3E-05 |
|
disease | 0.310 | None | 1.000 | 1 | 0 | 2011 | 2011 | ||||||||
|
R3H domain containing like | 0.931 | 0.115 | 1.9E-06 |
|
disease | 0.310 | None | 1.000 | 1 | 0 | 2011 | 2011 | ||||||||
|
sorting nexin 31 | 0.931 | 0.077 | 3.7E-13 |
|
disease | 0.310 | None | 1.000 | 1 | 0 | 2014 | 2014 | ||||||||
|
cyclin Pas1/PHO80 domain containing 1 | 0.931 | 0.115 | 7.6E-09 |
|
disease | 0.310 | None | 1.000 | 1 | 0 | 2013 | 2013 | ||||||||
|
tRNA methyltransferase 2 homolog A | 0.931 | 0.115 | 1.1E-08 |
|
disease | 0.310 | None | 1.000 | 1 | 0 | 2007 | 2007 | ||||||||
|
Retinal nonattachment, nonsyndromic congenital | 0.931 | 0.077 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2014 | 2014 | |||||||||
|
cortexin 3 | 0.931 | 0.077 | 0.14 |
|
disease | 0.320 | None | 1.000 | 1 | 0 | 2012 | 2015 | ||||||||
|
coiled-coil domain containing 86 | 0.931 | 0.154 | 1.7E-05 |
|
disease | 0.310 | None | 1.000 | 1 | 0 | 2013 | 2013 | ||||||||
|
cingulin like 1 | 0.931 | 0.038 | 4.7E-42 |
|
disease | 0.310 | None | 1.000 | 1 | 0 | 2014 | 2014 | ||||||||
|
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta pseudogene 5 | 0.931 | 0.077 |
|
disease | 0.310 | None | 1.000 | 1 | 0 | 2015 | 2015 | |||||||||
|
EF-hand calcium binding domain 11 | 0.931 | 0.115 | 2.3E-04 |
|
disease | 0.310 | None | 1.000 | 1 | 0 | 2014 | 2014 | ||||||||
|
regulating synaptic membrane exocytosis 3 | 0.931 | 0.038 | 1.5E-04 |
|
disease | 0.310 | None | 1.000 | 1 | 0 | 2009 | 2009 | ||||||||
|
phospholipase A2 group IVB | 0.890 | 0.154 | 1.1E-40 |
|
disease | 0.310 | None | 1.000 | 1 | 0 | 2005 | 2005 | ||||||||
|
protein tyrosine phosphatase non-receptor type 21 | 0.890 | 0.192 | 2.2E-12 |
|
disease | 0.310 | None | 1.000 | 1 | 0 | 2011 | 2011 | ||||||||
|
MSS51 mitochondrial translational activator | 0.890 | 0.154 | 3.3E-11 |
|
disease | 0.310 | None | 1.000 | 1 | 0 | 2011 | 2011 |