Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "P"

561 to 570 of 1361 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
561	5308	PITX2	Paired like homeodomain 2	ARP1, ASGD4, Brx1, IDG2, IGDS, IGDS2, IHG2, IRID2, Otlx2, PTX2, RGS, RIEG, RIEG1, RS	Aniridia, Anophthalmia/microphthalmia-esophageal atresia syndrome, Anterior segment dysgenesis, Anterior segment mesenchymal dysgenesis, Ataxia with deafness and vision loss, Atrial fibrillation, Atrial flutter, Axenfeld anomaly, Axenfeld-rieger syndrome, Blood coagulation disorder, Cardiac arrhythmia, Cardiac embolism, Cardioembolic stroke, Cardiovascular disease, Cataract View all (19 more)
562	5309	PITX3	Paired like homeodomain 3	ASGD1, ASMD, ASOD, CTPP4, CTRCT11, PTX3	Alzheimer disease, Anhedonia, Anophthalmia/microphthalmia-esophageal atresia syndrome, Anterior segment dysgenesis, Anterior segment mesenchymal dysgenesis, Atrial fibrillation, Cataract, Cataract-glaucoma syndrome, Congenital cataract, Congenital cataract anterior segment dysgenesis syndrome, Major depressive disorder, Posterior polar cataract, Microphthalmos, Posterior subcapsular cataract, Prostatic neoplasms, Schizophrenia View all (1 more)
563	9271	PIWIL1	Piwi like RNA-mediated gene silencing 1	CT80.1, HIWI, MIWI, PIWI	Alzheimer disease, Dementia, Male infertility, Metabolic syndrome
564	55124	PIWIL2	Piwi like RNA-mediated gene silencing 2	CT80, HILI, PIWIL1L, mili	Celiac disease, Male infertility, Male infertility single gene azoospermia, Paralytic strabismus
565	440822	PIWIL3	Piwi like RNA-mediated gene silencing 3	HIWI3	Colorectal cancer
566	143689	PIWIL4	Piwi like RNA-mediated gene silencing 4	HIWI2, MIWI2	Attention deficit hyperactivity disorder, Color vision deficiency, Colorectal cancer, Small cell lung carcinoma
567	64219	PJA1	Praja ring finger ubiquitin ligase 1	PRAJA1, RNF70	Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Craniofrontonasal dysplasia, Major depressive disorder, Parkinson disease, Psychiatric disorders, Schizophrenia
568	9867	PJA2	Praja ring finger ubiquitin ligase 2	Neurodap1, RNF131	Dupuytren contracture, Frontotemporal dementia, Nasal disorder, Psoriasis
569	494513	PJVK	Pejvakin	DFNB59	Isolated sensorineural deafness, Nonsyndromic hearing loss, Congenital ear anomaly, Deafness, Hearing impairment, Hearing loss, Hereditary hearing loss
570	5310	PKD1	Polycystin 1, transient receptor potential channel interacting	PBP, PC1, Pc-1, TRPP1, eliosin	Anhydramnios, Polycystic kidney disease, Polycystic kidney disease with tuberous sclerosis, Bladder exstrophy and epispadias complex, Caroli disease, Kidney disease, Congenital aneurysm of ascending aorta, Congenital kidney anomaly, Congenital clubfoot, Congenital hemivertebra, Crohn disease, Liver cyst, Cystic kidney disease, Dilated cardiomyopathy, Focal cortical dysplasia View all (13 more)

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