Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "P"

691 to 700 of 1032 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
691	56147	PCDHA1	Protocadherin alpha 1	PCDH-ALPHA1	Alzheimer disease, Bipolar disorder, Essential tremor, Gastroesophageal reflux disease, Insomnia, Major depressive disorder, Post-traumatic stress disorder, Schizophrenia
692	5617	PRL	Prolactin	GHA1	Amenorrhea, Anemia, Autism, Basal ganglia disease, Bradycardia, Carotid artery disease, Catalepsy, Chiari-frommel syndrome, Endometriosis, Erectile dysfunction, Growth hormone-secreting pituitary adenoma, Heart failure, Hyperproinsulinemia, Hypogonadism, Hypopituitarism View all (10 more)
693	5618	PRLR	Prolactin receptor	HPRL, MFAB, RI-PRLR, hPRLrI	Autism, Breast cancer, Carcinoma, Chiari-frommel syndrome, Endometriosis, Hyperprolactinemia, Hyperproinsulinemia, Hyperthyroidism, Hypothyroidism, Liver cirrhosis, Premature ovarian failure, Schizophrenia
694	5621	PRNP	Prion protein (Kanno blood group)	ASCR, AltPrP, CD230, CJD, GSS, KURU, PRIP, PrP, PrP27-30, PrP33-35C, PrPc, p27-30	Alzheimer disease, Autism, Cerebral amyloid angiopathy, Depression, Creutzfeldt-jakob disease, Dementia in huntington�s disease, Vascular dementia, Major depressive disorder, Hepatolenticular degeneration, Huntington disease, Insomnia, Liver cirrhosis, Mood disorder, Multiple sclerosis, Necrosis View all (3 more)
695	5624	PROC	Protein C, inactivator of coagulation factors Va and VIIIa	APC, PC, PROC1, THPH3, THPH4	Antiphospholipid syndrome, Arteritis, Asthma, Blood coagulation disorder, Central retinal vein occlusion, Ischemic stroke, Cerebral palsy, Hypertension, Kidney failure, Sepsis, Toxic shock syndrome, Venous thromboembolism, Venous thrombosis
696	5625	PRODH	Proline dehydrogenase 1	HSPOX2, PIG6, POX, PRODH1, TP53I6	Amino acid metabolism disorder, Bipolar disorder, Hyperprolinemia, Liver cirrhosis, Nervous system disease, Schizophrenia
697	5626	PROP1	PROP paired-like homeobox 1	CPHD2, PROP-1	Combined pituitary hormone deficiency, Desbuquois syndrome, Genetic panhypopituitarism, Hypogonadism, Hypopituitarism, Hypothyroidism, Panhypopituitarism, Pituitary dwarfism, Pituitary hormone deficiency
698	5627	PROS1	Protein S	PROS, PS21, PS22, PS23, PS24, PS25, PSA, THPH5, THPH6	Juvenile arthritis, Ischemic stroke, Clear cell renal cell carcinoma , Heart disease, Juvenile idiopathic arthritis, Kidney cancer, Optic atrophy, Oligoarticular juvenile idiopathic arthritis, Cerebral venous sinus thrombosis, Stevens-johnson syndrome, Venous thromboembolism
699	56288	PARD3	Par-3 family cell polarity regulator	ASIP, Baz, PAR3, PAR3alpha, PARD-3, PARD3A, PPP1R118, SE2-5L16, SE2-5LT1, SE2-5T2	Autism, Cardiac arrest, Acute lymphoblastic leukemia, Corneal astigmatism, Emphysema, Major depressive disorder, Neural tube defect, Nonalcoholic fatty liver disease, Oligodendroglioma, Premature ovarian failure, Parkinson disease, Prostatic neoplasm, Willis-ekbom disease, Severe acute respiratory syndrome
700	5629	PROX1	Prospero homeobox 1	-	Congenital heart disease, Diabetes mellitus, Diabetes mellitus type 2, Diabetic neuropathy, Diabetic retinopathy, Female infertility, Polycystic ovary syndrome, Psoriasis, Diabetes mellitus, type 2

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