Disease: Abnormality of retinal pigmentation
Source: ALL
Gene Uniprot Gene Full Name Protein Class pLI DSI v DPI v
ARL3 P36405 ADP ribosylation factor like GTPase 3 1.4E-03 0.603 0.615
BBS2 Q9BXC9 Bardet-Biedl syndrome 2 1.0E-17 0.565 0.654
CA4 P22748 carbonic anhydrase 4 7.1E-06 0.674 0.577
ERCC5 P28715 ERCC excision repair 5, endonuclease 2.7E-13 0.499 0.731
ERCC6 P0DP91 Q03468 ERCC excision repair 6, chromatin remodeling factor 5.2E-22 0.507 0.808
GUCA1B Q9UMX6 guanylate cyclase activator 1B 2.1E-04 0.682 0.423
LMNA P02545 lamin A/C 1.00 0.384 0.885
MITF O75030 melanocyte inducing transcription factor 0.98 0.499 0.808
ND6 P03923 NADH dehydrogenase, subunit 6 (complex I) 0.544 0.808
TRNF tRNA 0.582 0.731
TRNH tRNA 0.597 0.731
TRNL1 tRNA 0.534 0.731
TRNQ tRNA 0.590 0.731
TRNS1 tRNA 0.555 0.808
TRNS2 tRNA 0.579 0.731
TRNW tRNA 0.563 0.731
TNFRSF11B O00300 TNF receptor superfamily member 11b 0.16 0.422 0.808
PDE6A P16499 phosphodiesterase 6A 6.6E-25 0.691 0.269
PDE6B P35913 phosphodiesterase 6B 2.6E-27 0.626 0.346
PEX1 O43933 peroxisomal biogenesis factor 1 1.1E-14 0.538 0.769
PEX6 Q13608 peroxisomal biogenesis factor 6 6.3E-06 0.547 0.731
PEX7 O00628 peroxisomal biogenesis factor 7 8.2E-13 0.603 0.615
PEX10 O60683 peroxisomal biogenesis factor 10 5.4E-04 0.584 0.654
PEX13 Q92968 peroxisomal biogenesis factor 13 5.9E-05 0.597 0.654
PHYH O14832 phytanoyl-CoA 2-hydroxylase 2.4E-06 0.659 0.577