Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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9331 to 9340 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9331
P2Y receptor family member 10
LPS2, LYPSR2, P2Y10
Graves disease, Hypothyroidism, Rheumatoid arthritis

9332
Purinergic receptor P2Y11
P2Y11
Cataplexy and narcolepsy, Narcolepsy

9333
Purinergic receptor P2Y12
ADPG-R, BDPLT8, HORK3, P2T(AC), P2Y(12)R, P2Y(AC), P2Y(ADP), P2Y(cyc), P2Y12, SP1999
Asthma, Platelet-type bleeding disorder, Cerebrovascular disorder, Developmental disability, Diabetes mellitus type 2, Digestive system disease, Diverticular disease, Hemorrhage, Intellectual developmental disorder, Systemic lupus erythematosus, Myocardial infarction, Neurodevelopmental disorder, Peripheral arterial disease, Thrombocytopenia, Thrombosis
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9334
Purinergic receptor P2Y14
BPR105, GPR105, P2Y14
Diverticular disease, Insomnia, Irritable bowel syndrome

9335
Purinergic receptor P2Y2
HP2U, P2RU1, P2U, P2U1, P2UR, P2Y2, P2Y2R
Dental caries

9336
Pyrimidinergic receptor P2Y6
P2Y6
Lung cancer, Squamous cell carcinoma

9337
Prolyl 3-hydroxylase 1
GROS1, LEPRE1, OI8
Bone fragility with contractures, arterial rupture, and deafness, Desbuquois syndrome, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome

9338
Prolyl 3-hydroxylase 2
LEPREL1, MCVD, MLAT4
Breast cancer, Congenital heart septal defect, Marshall syndrome, Myopia, Osteoarthritis, Psoriasis, Psoriasis vulgaris, Psychiatric disorders, Retinitis pigmentosa, Urinary bladder cancer

9339
Prolyl 3-hydroxylase 3
GRCB, HSU47926, LEPREL2
Osteoarthritis, Pancreatic cancer

9340
P3R3URF-PIK3R3 readthrough
LOC110117498-PIK3R3
Breast cancer, Hearing loss, Lung cancer, Diabetes mellitus type 2