Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "P"
571 to 580 of 1361 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

571
Polycystin 1 like 1, transient receptor potential channel interacting
HTX8, PRO19563
Anxiety disorder, Autism, Cataract, Chylothorax, Liver cirrhosis, Heterotaxy syndrome, Iga nephropathy, Ovarian cancer, Scoliosis, Situs ambiguus, Situs inversus, Tetralogy of fallot

572
Polycystin 1 like 2 (gene/pseudogene)
PC1L2
Attention deficit hyperactivity disorder, Conduct disorder, Congenital left-sided heart lesions, Otosclerosis

573
Polycystin 1 like 3, transient receptor potential channel interacting
-
Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Conduct disorder, Coronary artery disease, Essential tremor, Gallbladder disease, Iga nephropathy, Myocardial infarction, Osteoarthritis, Prostate cancer, Diabetes mellitus type 2

574
Polycystin 2, transient receptor potential cation channel
APKD2, PC2, PKD4, Pc-2, TRPP2
Anhydramnios, Polycystic kidney disease, Breast cancer, Kidney disease, Degenerative disorder, Gout, Hypertension, Hyperuricemia, Intracranial aneurysm, Neurodegenerative disorder, Polycystic liver disease, Testicular hydrocele, Vascular disease

575
Polycystin 2 like 1, transient receptor potential cation channel
PCL, PKD2L, PKDL, TRPP3
Biliary tract cancer, Cardiovascular disease, Cataract, Coronary artery disease, Gallstones, Insomnia, Obesity, Skin disease, Squamous cell carcinoma

576
Polycystin 2 like 2, transient receptor potential cation channel
TRPP5
Atrial fibrillation, Auditory system disease

577
Protein kinase domain containing, cytoplasmic
RLSDF, SGK493, Vlk
Alzheimer disease, Androgenetic alopecia, Astrocytoma, Desbuquois syndrome, Hypospadias, Insomnia, Lung cancer, Rhizomelic limb shortening with dysmorphic features, Squamous cell carcinoma

578
PKHD1 ciliary IPT domain containing fibrocystin/polyductin
ARPKD, FCYT, FPC, PCYT, PKD4, TIGM1
Anhydramnios, Polycystic kidney disease, Cardiovascular disease, Caroli disease, Cholecystolithiasis, Congenital hypoplasia of aortic arch, Cystathionine beta-synthase deficiency, Glaucoma, Major depressive disorder, Metabolic syndrome, Oligodendroglioma, Open angle glaucoma, Periodontitis, Periportal fibrosis, Polycystic liver disease
View all (7 more)

579
PKHD1 like 1
DFNB124, PKHDL1
Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Female infertility, Multiple system atrophy, Obesity

580
CAMP-dependent protein kinase inhibitor alpha
PRKACN1
Major depressive disorder, Multiple sclerosis, Pulmonary arterial hypertension, Scoliosis, Systemic lupus erythematosus