Table 2 of Cheng, Mol Vis 2013; 19:955-969.


Table 2. Differentially Expressed Genes in the rd3 Retina involved in Human Retinal Diseases.

Fold change Gene symbol Gene name Retinal disease locus
+4.4 C3 Complement component 3 ARMD9, ASP
−2.6 Col9a1 Collagen, type IX, alpha 1
−2.5 Crb1 Crumbs homolog 1 LCA8, RP12
−2.3 Dmd Dystrophin, muscular dystrophy
−2.1 Fam161a Family with sequence similarity 161, member A RP28
−2.6 Fscn2 Fascin homolog 2, actin-bundling protein RP30
−2.3 Gnat1 Guanine nucleotide binding protein, alpha transducing 1 CSNBAD3
−2.1 Guca1b Guanylate cyclase activator 1B RP48
+2.9 Htra1 HtrA serine peptidase 1 ARMD7, PRSS11
−2.2 Opn1sw Opsin 1 (cone pigments), short-wave-sensitive BCP, CBT
−2.6 Pitpnm3 PITPNM family member 3 CORD5, NIR1
−4.2 Rgr Retinal G protein coupled receptor RP44
−2.2 Slc24a1 Solute carrier family 24 (sodium/ potassium/calcium exchanger), member 1 CSNB1D, NCKX, RODX
       
Genes assigned to human disease loci:
+7.6 C1qa Complement component 1, q subcomponent, alpha polypeptide LCA9, RP32
+4.9 C1qb Complement component 1, q subcomponent, beta polypeptide LCA9, RP32
+7.8 C1qc Complement component 1, q subcomponent, C chain NRL, RP27
+16.6 Cebpd CCAAT/enhancer binding protein (C/EBP), delta (Cebpd) CORD9
+2.3 Egr1 Early growth response 1 BSMD, PDE6A
−2.3 Pla2g7 Phospholipase A2, group BCMAD, RDS, RP7