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
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
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
CDHR1 Q96JP9 cadherin related family member 1 2.8E-21 0.670 0.308
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
COX1 P00395 cytochrome c oxidase subunit I Enzyme 0.441 0.885
COX2 P00403 cytochrome c oxidase subunit II Enzyme 0.352 0.962
COX3 P00414 cytochrome c oxidase III Enzyme 0.546 0.808
CRB1 P82279 crumbs cell polarity complex component 1 5.6E-16 0.570 0.654
CRX O43186 cone-rod homeobox Transcription factor 0.51 0.565 0.692
DHDDS Q86SQ9 dehydrodolichyl diphosphate synthase subunit Enzyme 0.25 0.468 0.885
DHX38 Q92620 DEAH-box helicase 38 Enzyme 2.1E-12 0.711 0.346
EDN3 P14138 endothelin 3 Signaling 2.5E-02 0.608 0.577