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 |