Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10411 to 10420 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10411
Pre-mRNA processing factor 38A
PRP38A, Prp38
Colorectal cancer

10412
Pre-mRNA processing factor 38B
NET1
Color vision deficiency, Nasopharyngeal neoplasms, Myopia

10413
Pre-mRNA splicing tri-snRNP complex factor PRPF4
HPRP4, HPRP4P, PRP4, Prp4p, RP70, SNRNP60
Retinitis pigmentosa

10414
Pre-mRNA processing factor 40A
FBP-11, FBP11, FLAF1, FNBP3, HIP-10, HIP10, HYPA, NY-REN-6, Prp40
Color vision deficiency, Diabetes mellitus type 2

10415
Pre-mRNA processing factor 40B
HYPC
Alzheimer disease, Attention deficit hyperactivity disorder, Schizophrenia, Substance abuse

10416
Pre-mRNA processing factor 6
ANT-1, ANT1, C20orf14, Prp6, RP60, SNRNP102, TOM, U5-102K, hPrp6
Retinitis pigmentosa

10417
Pre-mRNA processing factor 8
HPRP8, PRP8, PRPC8, RP13, SNRNP220
Retinitis pigmentosa, Cerebrovascular disorder, Choroideremia, Developmental disability, Glaucoma, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Stroke

10418
Peripherin
NEF4, PRPH1
Amyotrophic lateral sclerosis, Motor neuron disease

10419
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
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10420
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
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