Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "P"

1121 to 1130 of 1361 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1121	84726	PRRC2B	Proline rich coiled-coil 2B	BAT2L, BAT2L1, KIAA0515, LQFBS-1	Attention deficit hyperactivity disorder, Gout, Substance abuse
1122	23215	PRRC2C	Proline rich coiled-coil 2C	BAT2-iso, BAT2D1, BAT2L2, XTP2	Alzheimer disease, Glioma, Metabolic syndrome, Ocular sarcoidosis, Diabetes mellitus type 2
1123	5639	PRRG2	Proline rich and Gla domain 2	PRGP2	Schizophrenia
1124	79056	PRRG4	Proline rich and Gla domain 4	PRGP4, TMG4	Parkinson disease, Vascular disease
1125	80863	PRRT1	Proline rich transmembrane protein 1	C6orf31, DSPD1, IFITMD7, NG5, SynDIG4	Diabetes mellitus type 2
1126	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
1127	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 neoplasms, Retrognathia, Venous thromboembolism View all (2 more)
1128	51450	PRRX2	Paired related homeobox 2	PMX2, PRX2	Color vision deficiency
1129	5644	PRSS1	Serine protease 1	TRP1, TRY1, TRY4, TRYP1	Hereditary chronic pancreatitis, Pancreatitis, Cystic fibrosis, Pancreatic neoplasms, Pancreatic trypsinogen deficiency, Sarcoidosis, Vitamin d dependent rickets
1130	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

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