Genes | GeDiPNet - Gene Disease Pathway & Associations

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10471 to 10480 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
10471	58497	PRUNE1	Prune exopolyphosphatase 1	DRES-17, DRES17, H-PRUNE, HTCD37, NMIHBA, PRUNE	Gestational diabetes, Neurodevelopmental disorder, Diabetes mellitus type 2
10472	158471	PRUNE2	Prune homolog 2 with BCH domain	BMCC1, BNIPXL, C9orf65, KIAA0367	Central nervous system cancer, Cervical cancer, Dental caries, Glioblastoma, Glioma, Skin disease, Upper aerodigestive tract neoplasm
10473	57716	PRX	Periaxin	CMT4F	Charcot-marie-tooth disease, Congenital cataract, Dejerine-sottas disease, Distal spinal muscular atrophy, Gaucher disease, Hereditary motor and sensory neuropathies, Hereditary sensory and motor neuropathy, Hypertrophic neuropathy, Peripheral neuropathy, Peroneal muscle atrophy, Roussy-levy syndrome, Spinocerebellar ataxia
10474	84293	PRXL2A	Peroxiredoxin like 2A	Adrx, C10orf58, FAM213A, PAMM	Atrial fibrillation, Cataract, Gout, Heart failure, Hypertension, Peptic ulcer disease, Sarcoidosis
10475	127281	PRXL2B	Peroxiredoxin like 2B	C1orf93, FAM213B	Asthma, Autoimmune disease, Crohn disease, Inflammatory bowel disease, Multiple sclerosis, Rheumatoid arthritis, Ulcerative colitis
10476	195827	PRXL2C	Peroxiredoxin like 2C	AAED1, C9orf21	Gastric cancer
10477	5660	PSAP	Prosaposin	GLBA, PARK24, PSAPD, SAP1, SAP2	Asthma, Atypical femoral fracture, Gaucher disease, Parkinson disease, Bipolar disorder, Combined psap deficiency, Combined saposin deficiency, Coronary artery disease, Deafness, Eosinophilia, Metachromatic leukodystrophy, Major depressive disorder, Neuromuscular disease, Hereditary parkinson disease, Retinitis pigmentosa-deafness syndrome, Usher syndrome View all (1 more)
10478	29968	PSAT1	Phosphoserine aminotransferase 1	EPIP, NLS2, PSA, PSAT, PSATD	Attention deficit hyperactivity disorder, Non-small-cell lung carcinoma, Color vision deficiency, Desbuquois syndrome, Major depressive disorder, Obesity, Schizophrenia, Scoliosis, Myopia, Substance abuse, Diabetes mellitus type 2
10479	8000	PSCA	Prostate stem cell antigen	PRO232, lncPSCA	Anorexia nervosa, Biliary tract cancer, Bipolar disorder, Breast cancer, Cancer, Cervical cancer, Colorectal cancer, Curling ulcer, Diffuse gastric adenocarcinoma, Duodenal ulcer, Endometrial cancer, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Gastric ulcer View all (15 more)
10480	5662	PSD	Pleckstrin and Sec7 domain containing	EFA6, EFA6A, PSD1, TYL	Alzheimer disease, Common variable immunodeficiency, Schizophrenia

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