10461
|
|
|
Pre-mRNA processing factor 40B |
HYPC |
|
10462
|
|
|
Pre-mRNA processing factor 6 |
ANT-1, ANT1, C20orf14, Prp6, RP60, SNRNP102, TOM, U5-102K, hPrp6 |
|
10463
|
|
|
Pre-mRNA processing factor 8 |
HPRP8, PRP8, PRPC8, RP13, SNRNP220 |
|
10464
|
|
|
Peripherin |
NEF4, PRPH1 |
|
10465
|
|
|
Peripherin 2 |
AOFMD, AVMD, CACD2, DS, MDBS1, PRPH, RDS, RP7, TSPAN22, rd2 |
Distal myopathy, Bestrophinopathy, Butterfly-shaped pigmentary macular dystrophy, Central areolar choroidal dystrophy, Choroidal dystrophy, Choroidal sclerosis, Choroideremia, Cone dystrophy, Cone-rod dystrophy, Doyne honeycomb retinal dystrophy, Leber congenital amaurosis, Macular degeneration, Macular dystrophy, Optic atrophy, Patterned macular dystrophy, Retinitis pigmentosa, Retinitis pigmentosa, digenic, Retinitis punctata albescens, Stargardt disease, Usher syndrome, Vitelliform macular dystrophyView all (6 more) |
10466
|
|
|
Phosphoribosyl pyrophosphate synthetase 1 |
ARTS, CMTX5, DFN2, DFNX1, PPRibP, PRS-I, PRSI |
Gouty arthritis, Arts syndrome, Ataxia with deafness and vision loss, Charcot-marie-tooth disease, Charcot-marie-tooth disease, x-linked, Deafness, x-linked, Dejerine-sottas disease, Gout, Hereditary hearing loss, Hereditary motor and sensory neuropathies, Hypertrophic neuropathy, Prpp synthetase superactivity, Optic atrophy, Peroneal muscle atrophy, Retinitis pigmentosa, Roussy-levy syndrome, X-linked intellectual disability, X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome, X-linked nonsyndromic hearing lossView all (4 more) |
10467
|
|
|
Phosphoribosyl pyrophosphate synthetase 1 like 1 |
PRPS1, PRPS3, PRPSL, PRS-III |
|
10468
|
|
|
Phosphoribosyl pyrophosphate synthetase 2 |
PRSII |
|
10469
|
|
|
Phosphoribosyl pyrophosphate synthetase associated protein 1 |
PAP39 |
|
10470
|
|
|
Phosphoribosyl pyrophosphate synthetase associated protein 2 |
PAP41 |
|
