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
AHI1 Q8N157 Abelson helper integration site 1 1.1E-25 0.513 0.846
AIPL1 Q9NZN9 aryl hydrocarbon receptor interacting protein like 1 Chaperone 1.2E-05 0.644 0.346
ATF6 P18850 activating transcription factor 6 3.2E-07 0.516 0.846
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
CACNA1F O60840 calcium voltage-gated channel subunit alpha1 F Ion channel 1.2E-05 0.595 0.500
CACNA2D4 Q7Z3S7 calcium voltage-gated channel auxiliary subunit alpha2delta 4 Ion channel 1.5E-34 0.716 0.269
CDHR1 Q96JP9 cadherin related family member 1 2.8E-21 0.670 0.308
CEP120 Q8N960 centrosomal protein 120 4.1E-15 0.564 0.731
CEP290 O15078 centrosomal protein 290 1.1E-60 0.517 0.769
CFAP410 O43822 cilia and flagella associated protein 410 3.3E-07 0.633 0.615
CLRN1 P58418 clarin 1 1.7E-08 0.633 0.423
CNGA3 Q16281 cyclic nucleotide gated channel subunit alpha 3 Ion channel 8.0E-20 0.650 0.154
CNGB3 Q9NQW8 cyclic nucleotide gated channel subunit beta 3 Ion channel 7.8E-19 0.633 0.192
CNNM4 Q6P4Q7 cyclin and CBS domain divalent metal cation transport mediator 4 2.9E-07 0.695 0.346
COX3 P00414 cytochrome c oxidase III Enzyme 0.546 0.808
COX7B P24311 cytochrome c oxidase subunit 7B 0.67 0.595 0.654
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
DRAM2 Q6UX65 DNA damage regulated autophagy modulator 2 1.4E-04 0.729 0.462
ELMO2 Q96JJ3 engulfment and cell motility 2 Signaling 1.0E-05 0.729 0.538
ERCC1 P07992 ERCC excision repair 1, endonuclease non-catalytic subunit Enzyme 1.6E-07 0.445 0.846
ERCC2 P18074 ERCC excision repair 2, TFIIH core complex helicase subunit Enzyme 7.1E-20 0.420 0.846