Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "P"

1131 to 1140 of 1369 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1131	80863	PRRT1	Proline rich transmembrane protein 1	C6orf31, DSPD1, IFITMD7, NG5, SynDIG4	Diabetes mellitus, type 2
1132	112476	PRRT2	Proline rich transmembrane protein 2	BFIC2, BFIS2, DSPB3, DYT10, EKD1, FICCA, ICCA, IFITMD1, PKC	Benign infantile epilepsy, Childhood-onset glut1 deficiency syndrome 2, Familial infantile convulsions with paroxysmal choreoathetosis, Dystonia, Episodic kinesigenic dyskinesia, Paroxysmal dystonia, Generalized epilepsy with febrile seizures plus, Global developmental delay, Hemiplegic migraine, Intellectual developmental disorder, Neurodevelopmental disorder, Paroxysmal dyskinesia, Paroxysmal dystonic choreoathetosis, Paroxysmal nonkinesigenic dyskinesia, Seizures
1133	5396	PRRX1	Paired related homeobox 1	AGOTC, PHOX1, PMX1, PRX-1, PRX1	Agnathia-otocephaly, Alzheimer disease, Aortic stenosis, Aortic valve disease, Atrial fibrillation, Atrial flutter, Cardiac arrhythmia, Cardiac embolism, Cardioembolic stroke, Craniosynostosis, Dementia, Demyelinating diseases, Dysgnathia complex, Otosclerosis, Prostatic neoplasm, Retrognathia, Venous thromboembolism View all (2 more)
1134	51450	PRRX2	Paired related homeobox 2	PMX2, PRX2	Color vision deficiency
1135	5644	PRSS1	Serine protease 1	TRP1, TRY1, TRY4, TRYP1	Hereditary chronic pancreatitis, Pancreatitis, Cystic fibrosis, Pancreatic neoplasm, Pancreatic trypsinogen deficiency, Sarcoidosis, Vitamin d-dependent rickets
1136	8492	PRSS12	Serine protease 12	BSSP-3, BSSP3, MRT1	Alzheimer disease, Nonsyndromic intellectual disability, Congenital heart disease, Gestational diabetes, Insomnia, Intellectual developmental disorder, Willis-ekbom disease
1137	10279	PRSS16	Serine protease 16	TSSP	Alzheimer disease, Autism, Gout, Insomnia, Non-melanoma skin carcinoma, Psoriasis, Rheumatoid arthritis, Schizophrenia, Diabetes mellitus, type 1
1138	5645	PRSS2	Serine protease 2	TRY2, TRY8, TRYP2	Hereditary chronic pancreatitis, Pancreatitis, Oligodendroglioma
1139	64063	PRSS22	Serine protease 22	BSSP-4, SP001LA, hBSSP-4	Erythematosquamous dermatosis, Seborrheic dermatitis
1140	11098	PRSS23	Serine protease 23	SIG13, SPUVE, ZSIG13	Alzheimer disease, Obstructive pulmonary disease, Color vision deficiency, Endocrine system disease, Exudative retinopathy, Exudative vitreoretinopathy, Glaucoma, Hepatocellular carcinoma, Melanoma, Open angle glaucoma, Prostate cancer, Retinopathy of prematurity

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