Autosomal Dominant Retinitis Pigmentosa
| Gene Symbol | Aliases | Full Gene Name |
Chr | Disorder | Mode of Inheritance | OMIM | HGNC ID |
| CA4 | CAIV; Car4; RP17 | carbonic anhydrase IV | 17q23 | AD RP | autosomal dominant | 114760 | HGNC:1375 |
| FSCN2 | RFSN; RP30 | fascin homolog 2, actin-bundling protein, retinal (Strongylocent- rotus purpuratus) |
17q25 | AD RP | autosomal dominant | 607643 | HGNC:3960 |
| IMPDH1 | DKFZp781N0678; IMPD; IMPD1; LCA11; RP10; sWSS2608 | IMP (inosine monophosphate) dehydrogenase 1 | 7q31.3- q32 |
AD RP | autosomal dominant | 146690 | HGNC:6052 |
| NRL | D14S46E; NRL-MAF; RP27 | neural retina leucine zipper | 14q11.1- q11.2 |
AD RP | autosomal dominant | 162080 | HGNC:8002 |
| PRPF3 | HPRP3; HPRP3P; PRP3; Prp3p; RP18 | PRP3 pre-mRNA processing factor 3 homolog | 1q21.1 | AD RP | autosomal dominant | 607301 | HGNC:17348 |
| PRPF31 | DKFZp566J153; NY-BR-99; PRP31; RP11 | PRP31 pre-mRNA processing factor 31 homolog |
19q13.42 | AD RP | autosomal dominant | 606419 | HGNC:15446 |
| PRPF8 | HPRP8; PRP8; PRPC8; RP13 | PRP8 pre-mRNA processing factor 8 homolog |
17p13.3 | AD RP | autosomal dominant | 607300 | HGNC:17340 |
| PRPH2 | AOFMD; AVMD; PRPH; RP7; TSPAN22; rd2; RDS | peripherin 2 (retinal degeneration, slow) |
6p21.2- p12.3 |
AD RP | autosomal dominant | 179605 | HGNC:9942 |
| RHO | CSNBAD1; MGC138309; MGC138311; OPN2; RP4 | rhodopsin | 3q21-q24 | AD RP | autosomal dominant | 180380 | HGNC:10012 |
| ROM1 | ROM; ROSP1; RP7; TSPAN23 | retinal outer segment membrane protein 1 |
11q13 | AD RP | autosomal dominant | 180721 | HGNC:10254 |
| RP1 | DCDC4A; FLJ50293; FLJ55454; FLJ79410; ORP1 | retinitis pigmentosa 1 |
8q12.1 | AD RP | autosomal dominant | 603937 | HGNC:10263 |
| RP9 | PAP-1 | retinitis pigmentosa 9 |
7p14.3 | AD RP | autosomal dominant | 607331 | HGNC:10288 |
| CRX | CORD2; CRD; LCA7; OTX3 | cone-rod homeobox |
19q13.3 | AD RP | autosomal dominant | 602225 | HGNC:2383 |
| TOPORS | RP11-205M20.5; LUN; P53BP3; RP31; TP53BPL | topoisomerase I binding, arginine/ serine-rich |
9p21 | AD RP | autosomal dominant | 609507 | HGNC:21653 |
| NR2E3 | ESCS; MGC49976; PNR; RNR; RP37; rd7 | nuclear receptor subfamily 2, group E, member 3 |
15q22.32 | AD RP | autosomal dominant | 604485 | HGNC:7974 |
| KLHL7 | RP42; KLHL6; SBBI26 | kelch-like 6, kelch-like 7, kelch/BTB, retinitis pigmentosa 42 |
7p15.3 | AD RP | autosomal dominant | 611119 | HGNC:15646 |
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