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. | ||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
VPS8 subunit of CORVET complex | 1.000 | 0.077 | 5.1E-08 |
|
disease | 0.500 | limited | 1.000 | 3 | 0 | 1996 | 2016 | ||||||||
|
glycerophosphodiester phosphodiesterase domain containing 3 | 1.000 | 0.077 | 1.7E-15 |
|
disease | 0.300 | None | 1.000 | 3 | 0 | 2005 | 2007 | ||||||||
|
PAT1 homolog 2 | 1.000 | 1.2E-11 |
|
disease | 0.400 | None | 1.000 | 2 | 9 | 2017 | 2017 | |||||||||
|
tubulin beta 8 class VIII | 1.000 | 1.8E-02 |
|
disease | 0.600 | None | 1.000 | 2 | 14 | 2016 | 2016 | |||||||||
|
glucosamine-6-phosphate deaminase 1 | 1.000 | 0.077 | 1.6E-07 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2014 | 2014 | ||||||||
|
gap junction protein epsilon 1 | 1.000 | 0.077 | 0.11 |
|
group | 0.310 | None | 1.000 | 1 | 0 | 2011 | 2011 | ||||||||
|
thiosulfate sulfurtransferase like domain containing 3 | 1.000 | 0.077 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2014 | 2014 | |||||||||
|
Chromosome 22q11.2 deletion syndrome, distal | 1.000 | 0.038 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2012 | 2012 | |||||||||
|
dystonia 17 | 1.000 | 0.038 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2008 | 2008 | |||||||||
|
spastic paraplegia 41 (autosomal dominant) | 1.000 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2008 | 2008 | ||||||||||
|
microRNA 1273c | 1.000 | 0.077 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2015 | 2015 | |||||||||
|
microRNA 1273c | 1.000 | 0.077 |
|
group | 0.300 | None | 1.000 | 1 | 0 | 2015 | 2015 | |||||||||
|
microRNA 1273c | 1.000 | 0.077 |
|
phenotype | 0.300 | None | 1.000 | 1 | 0 | 2015 | 2015 | |||||||||
|
microRNA 1273c | 1.000 | 0.077 |
|
phenotype | 0.300 | None | 1.000 | 1 | 0 | 2015 | 2015 | |||||||||
|
BMPR1B divergent transcript | 1.000 | 0.038 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2005 | 2005 | |||||||||
|
formin binding protein 1 pseudogene 1 | 1.000 | 0.038 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2018 | 2018 | |||||||||
|
microRNA 4482 | 1.000 | 0.077 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2017 | 2017 | |||||||||
|
NUTM2B antisense RNA 1 | 1.000 | 0.115 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2019 | 2019 | |||||||||
|
microRNA 6881 | 1.000 | 0.077 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2017 | 2017 | |||||||||
|
ATP binding cassette subfamily A member 10 | 1.000 | 0.077 | 7.7E-34 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2012 | 2012 | ||||||||
|
ATP binding cassette subfamily A member 10 | 1.000 | 0.077 | 7.7E-34 |
|
group | 0.300 | None | 1.000 | 1 | 0 | 2012 | 2012 | ||||||||
|
cell growth regulator with EF-hand domain 1 | 1.000 | 0.077 | 4.7E-08 |
|
group | 0.300 | None | 1.000 | 1 | 0 | 2017 | 2017 | ||||||||
|
cell growth regulator with EF-hand domain 1 | 1.000 | 0.077 | 4.7E-08 |
|
disease | 0.300 | None | 1.000 | 1 | 0 | 2017 | 2017 | ||||||||
|
Macular dystrophy, North Carolina type | 1.000 | 0.077 |
|
disease | 0.500 | None | 1.000 | 1 | 0 | 2016 | 2016 | |||||||||
|
DIAPH2 antisense RNA 1 | 1.000 | 0.038 |
|
phenotype | 0.300 | None | 1.000 | 1 | 0 | 2008 | 2008 |