Disease: Abnormality of retinal pigmentation
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
ADAM9 Q13443 ADAM metallopeptidase domain 9 Enzyme 2.9E-02 0.560 0.654
AGBL5 Q8NDL9 ATP/GTP binding protein like 5 Enzyme 2.4E-08 0.711 0.269
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
AKT1 P31749 AKT serine/threonine kinase 1 Kinase 0.98 0.311 0.962
APC P25054 APC regulator of WNT signaling pathway 1.00 0.373 0.962
ARHGEF18 Q6ZSZ5 Rho/Rac guanine nucleotide exchange factor 18 1.8E-03 0.700 0.308
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
BBS2 Q9BXC9 Bardet-Biedl syndrome 2 1.0E-17 0.565 0.654
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
CBS P0DN79 P35520 cystathionine beta-synthase Enzyme 3.1E-05 0.465 0.885
CDHR1 Q96JP9 cadherin related family member 1 2.8E-21 0.670 0.308
CEP164 Q9UPV0 centrosomal protein 164 4.8E-27 0.711 0.462
CEP290 O15078 centrosomal protein 290 1.1E-60 0.517 0.769
CERKL Q49MI3 ceramide kinase like 9.8E-25 0.678 0.308
CLRN1 P58418 clarin 1 1.7E-08 0.633 0.423
CNGA1 P29973 cyclic nucleotide gated channel subunit alpha 1 Ion channel 2.8E-11 0.695 0.269
CNGB1 Q14028 cyclic nucleotide gated channel subunit beta 1 Ion channel 1.8E-37 0.628 0.538
CNGB3 Q9NQW8 cyclic nucleotide gated channel subunit beta 3 Ion channel 7.8E-19 0.633 0.192