561
|
|
|
RNA polymerase II associated protein 2 |
C1orf82, Rtr1 |
|
562
|
|
|
RNA polymerase II associated protein 3 |
Tah1, hSpagh |
|
563
|
|
|
Retinoid isomerohydrolase RPE65 |
BCO3, LCA2, RP20, mRPE65, p63, rd12, sRPE65 |
Leber congenital amaurosis, Autism, Retinitis pigmentosa, Blindness, Cone-rod dystrophy, Congenital blindness, Congenital nystagmus, Eye disease, Glaucoma, Global developmental delay, Neurodevelopmental disorder, Nystagmus, Open angle glaucoma, Leber hereditary optic neuropathy, Retinal degeneration, Retinitis pigmentosa with choroidal involvement, Rod-cone dystrophy, Retinopathy, Stargardt diseaseView all (4 more) |
564
|
|
|
Ribosome production factor 1 homolog |
BXDC5 |
|
565
|
|
|
Ribosome production factor 2 homolog |
BXDC1, bA397G5.4 |
|
566
|
|
|
Retinitis pigmentosa GTPase regulator |
COD1, CORDX1, CRD, PCDX, RP15, RP3, XLRP3, orf15 |
Ciliary dyskinesia, Cone dystrophy, Cone dystrophy, x-linked, Cone-rod dystrophy, Cone-rod dystrophy, x-linked, Esophageal atresia, Hearing impairment, Hearing loss, Leber congenital amaurosis, Macular degeneration, Atrophic macular degeneration, Macular dystrophy, Night blindness, congenital stationary, Optic atrophy, Ciliary dyskinesia with retinitis pigmentosa, Respiratory system infectious disease, Retinal degeneration, Retinitis pigmentosa, Retinitis pigmentosa, x-linked, and sinorespiratory infections with or without deafness, Retinopathy, X-linked cone-rod dystrophyView all (6 more) |
567
|
|
|
RPGR interacting protein 1 |
CORD13, LCA6, RGI1, RGRIP, RPGRIP, RPGRIP1d |
Leber congenital amaurosis, Bardet-biedl syndrome, Cone dystrophy, Cone-rod dystrophy, Joubert syndrome, Meckel-gruber syndrome, Nystagmus, Optic atrophy, Leber hereditary optic neuropathy, Retinitis pigmentosa, Skin disease |
568
|
|
|
RPGRIP1 like |
COACH3, CORS3, FTM, JBTS7, MKS5, NPHP8, PPP1R134 |
Anencephaly, Aprosencephaly, Attention deficit hyperactivity disorder, Autism, Bardet-biedl syndrome, Barrett esophagus, Bipolar disorder, Cerebellar ataxia, Cerebellar diseases, Ciliary dyskinesia, Ciliopathy, Coach syndrome, Color vision deficiency, Cystic kidney disease, Vascular dementia, Desbuquois syndrome, Disorder of eye, Esophageal disease, Eye disease, Aplasia of the vermis, Gastroesophageal reflux disease, Joubert syndrome, Kidney disease, Leber congenital amaurosis, Leprosy, Meckel-gruber syndrome, Intellectual developmental disorder, Metabolic syndrome, Nephronophthisis, Optic atrophy, Retinal degeneration, Retinitis pigmentosa, Diabetes mellitus type 2, VitiligoView all (19 more) |
569
|
|
|
Rabphilin 3A |
- |
Alzheimer disease, Neurodevelopmental disorder, Congenital myasthenic syndrome, Coronary artery disease, Epilepsy, Esophageal cancer, Generalized epilepsy, Gout, Insomnia, Metabolic syndrome, Myasthenic syndrome, Non-specific syndromic intellectual disability, Open angle glaucoma, Partial epilepsy, Diabetes mellitus type 2, Upper aerodigestive tract neoplasmView all (1 more) |
570
|
|
|
Rabphilin 3A like (without C2 domains) |
NOC2 |
|
