Genes | GeDiPNet - Gene Disease Pathway & Associations

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10371 to 10380 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
10371	5550	PREP	Prolyl endopeptidase	PE, PEP	Amnesia, Androgenetic alopecia, Asthma, Colorectal cancer, Duchenne muscular dystrophy, Glomerulonephritis, Retrograde amnesia, Stomach neoplasms
10372	9581	PREPL	Prolyl endopeptidase like	CMS22	Hypotonia-cystinuria syndrome, Congenital myasthenic syndrome, Cystine urolithiasis, Cystinuria, Intellectual developmental disorder, Myasthenic syndrome
10373	57580	PREX1	Phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 1	P-REX1	Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Breast cancer, Cancer, Cardiovascular disease, Central serous retinopathy, Colorectal cancer, Colonic neoplasms, Colorectal adenoma, Coronary artery disease, Estrogen-receptor negative breast cancer, Hypertension, Hypothyroidism, Lung cancer View all (16 more)
10374	80243	PREX2	Phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 2	DEP.2, DEPDC2, P-REX2, PPP1R129	Cerebral arteriovenous malformations, Bladder exstrophy, Dry eye syndrome, Pancreatic cancer
10375	5551	PRF1	Perforin 1	HPLH2, P1, PFP	Aplastic anemia, Autism, Autoinflammatory syndrome, Crohn disease, Hemophagocytic lymphohistiocytosis, Hereditary hemophagocytic lymphohistiocytosis, Multiple sclerosis, Nonalcoholic fatty liver disease
10376	5553	PRG2	Proteoglycan 2, pro eosinophil major basic protein	BMPG, MBP, MBP1, proMBP	Alzheimer disease, Autism
10377	10394	PRG3	Proteoglycan 3, pro eosinophil major basic protein 2	MBP2, MBPH	Hypertrophic cardiomyopathy
10378	10216	PRG4	Proteoglycan 4	CACP, HAPO, JCAP, MSF, SZP	Arthrogryposis multiplex congenita, Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, Contracture, Hyperplasia, Pena-shokeir syndrome , Pericarditis, Secondary malignant neoplasm
10379	144165	PRICKLE1	Prickle planar cell polarity protein 1	EPM1B, RILP	Alzheimer disease, Arthrogryposis multiplex congenita, Autoimmune thyroid disease, Epilepsy, Progressive myoclonic epilepsy, Rolandic epilepsy, Graves disease, Hashimoto disease, Intellectual developmental disorder, Multiple sclerosis, Pena-shokeir syndrome , Unverricht-lundborg syndrome
10380	166336	PRICKLE2	Prickle planar cell polarity protein 2	EPM5	Alzheimer disease, Asthma, Nonsyndromic intellectual disability, Endocrine neoplasms, Breast cancer, Colorectal cancer, Neurodevelopmental disorder, Dementia, Digestive system disease, Rolandic epilepsy, Generalized anxiety disorder, Glaucoma, Hyperopia, Liver neoplasms, Myoclonic epilepsy View all (10 more)

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