Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10481 to 10490 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10481
PRR23 family member E
C3orf56
Amyotrophic lateral sclerosis

10482
Proline rich 3
CAT56
Graves disease, Hypothyroidism, Insomnia, Psoriasis, Rheumatoid arthritis

10483
Proline rich 36
-
Schizophrenia

10484
Proline rich 5
FLJ20185k, PP610, PROTOR-1, PROTOR1
Color vision deficiency

10485
PRR5-ARHGAP8 readthrough
-
Alzheimer disease, Binge eating disorder, Colonic neoplasms, Color vision deficiency, Major depressive disorder, Orofacial cleft, Stomach neoplasms

10486
Proline rich 5 like
PROTOR2
Asthma, Eczema, Crohn disease, Inflammatory bowel disease, Inflammatory skin disease, Multiple sclerosis, Myositis, Oligoarticular juvenile idiopathic arthritis, Polyarticular juvenile idiopathic arthritis, Psoriasis, Respiratory system disease, Rheumatoid arthritis, Juvenile idiopathic arthritis, Ulcerative colitis

10487
Proline rich coiled-coil 1
-
Hypertension

10488
Proline rich coiled-coil 2A
BAT2, D6S51, D6S51E, G2
Autism, Autoimmune disease, Celiac disease, Cervical cancer, Coronary artery disease, Crohn disease, Diabetes mellitus type 1, Apolipoprotein b hypobetalipoproteinemia, Gallstones, Glomerulonephritis, Hypertension, Inflammatory bowel disease, Irritable bowel syndrome, Major depressive disorder, Membranous glomerulonephritis
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10489
Proline rich coiled-coil 2B
BAT2L, BAT2L1, KIAA0515, LQFBS-1
Attention deficit hyperactivity disorder, Gout, Substance abuse

10490
Proline rich coiled-coil 2C
BAT2-iso, BAT2D1, BAT2L2, XTP2
Alzheimer disease, Glioma, Metabolic syndrome, Ocular sarcoidosis, Diabetes mellitus type 2