Table 4.
EST clusters mapping to locations containing the locus for an inherited retinal disease (in chromosomal order)
| EST name(s) | Cluster size | EST location(s) | Disease symbol or type | Disease location | OMIM Number |
|---|---|---|---|---|---|
| 161757,164265 | 4,3 | 1q21-q22 | RP18 | 1q13-q23 | 601414 |
| 158775 | 7 | 2q33.1 | RP26 | 2q31-q33 | |
| 158800 | 3 | 3q27.3-q28 | OPA1 | 3q28-q29 | 165500 |
| 138537 | 4 | 6q25.3-q26 | RCD1 | 6q25-q26 | 180020 |
| 138645 | 6 | 7p14.1 | RP9 | 7p13-p15 | 180104 |
| 159003,163847 | 8,3 | 10q21.1 | congenital retinal nonattachment | 10q21 | 221900 |
| 197125 | 3 | 11q14.21 | EVR1,FEVR; VRNI | 11q13-q23 | 133780 193235 |
| 38621,125808,16422 | 4,8,3 | 13q33.3-qter | STGD2 | 13q34 | 153900 |
| 158844 | 4 | 15q24.3 | syndromic retinal degeneration | 15q24 | [6] |
| 164707 | 3 | 18q21.2 | CORD1 | 18q21.1-q21.3 | 600624 |