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 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

571
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)

572
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

573
Polycystin 1 like 2 (gene/pseudogene)
PC1L2
Attention deficit hyperactivity disorder, Conduct disorder, Congenital left-sided heart lesions, Dermatophytosis, Otosclerosis

574
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

575
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, Liver cirrhosis, Neurodegenerative disorder, Polycystic liver disease, Testicular hydrocele, Vascular disease

576
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

577
Polycystin 2 like 2, transient receptor potential cation channel
TRPP5
Atrial fibrillation, Auditory system disease

578
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

579
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)

580
PKHD1 like 1
DFNB124, PKHDL1
Isolated sensorineural deafness, Nonsyndromic hearing loss, Deafness, Female infertility, Multiple system atrophy, Obesity