Disease: Rod-Cone Dystrophy
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
ABCA4 P78363 ATP binding cassette subfamily A member 4 Transporter 5.3E-48 0.493 0.769
ACOX1 Q15067 acyl-CoA oxidase 1 Enzyme 6.2E-02 0.610 0.731
ADGRV1 Q8WXG9 adhesion G protein-coupled receptor V1 G-protein coupled receptor 3.2E-39 0.572 0.731
AHI1 Q8N157 Abelson helper integration site 1 1.1E-25 0.513 0.846
AHR P35869 aryl hydrocarbon receptor Transcription factor 1.00 0.410 0.923
AIPL1 Q9NZN9 aryl hydrocarbon receptor interacting protein like 1 Chaperone 1.2E-05 0.644 0.346
ARL2BP Q9Y2Y0 ADP ribosylation factor like GTPase 2 binding protein 3.3E-05 0.647 0.654
ARL3 P36405 ADP ribosylation factor like GTPase 3 1.4E-03 0.603 0.615
ARL6 Q9H0F7 ADP ribosylation factor like GTPase 6 1.0E-02 0.636 0.462
BBIP1 A8MTZ0 BBSome interacting protein 1 4.2E-03 0.695 0.423
BBS1 Q8NFJ9 Bardet-Biedl syndrome 1 3.4E-12 0.593 0.692
BBS10 Q8TAM1 Bardet-Biedl syndrome 10 1.7E-12 0.644 0.538
BBS12 Q6ZW61 Bardet-Biedl syndrome 12 2.3E-07 0.674 0.462
BBS2 Q9BXC9 Bardet-Biedl syndrome 2 1.0E-17 0.565 0.654
BBS4 Q96RK4 Bardet-Biedl syndrome 4 1.5E-16 0.647 0.615
BBS5 Q8N3I7 Bardet-Biedl syndrome 5 4.8E-06 0.659 0.577
BBS7 Q8IWZ6 Bardet-Biedl syndrome 7 7.1E-09 0.682 0.462
BBS9 Q3SYG4 Bardet-Biedl syndrome 9 4.2E-17 0.615 0.577
BEST1 O76090 bestrophin 1 Ion channel 1.8E-12 0.465 0.885
C8orf37 Q96NL8 chromosome 8 open reading frame 37 2.4E-05 0.628 0.538
CA4 P22748 carbonic anhydrase 4 7.1E-06 0.674 0.577
CACNA1F O60840 calcium voltage-gated channel subunit alpha1 F Ion channel 1.2E-05 0.595 0.500
CDH23 Q9H251 cadherin related 23 3.2E-06 0.539 0.769
CDHR1 Q96JP9 cadherin related family member 1 2.8E-21 0.670 0.308
CEP290 O15078 centrosomal protein 290 1.1E-60 0.517 0.769