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"
321 to 330 of 1361 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

321
Decaprenyl diphosphate synthase subunit 2
C6orf210, COQ10D3, COQ1B, DLP1, bA59I9.3, hDLP1
Coenzyme q10 deficiency, Focal glomerulosclerosis, Kidney disease, Leigh syndrome, Nephrotic syndrome, Prostate cancer

322
Pancreatic and duodenal homeobox 1
GSF, IDX-1, IPF1, IUF1, MODY4, PAGEN1, PDX-1, STF-1
Ischemic stroke, Congenital hypoplasia of pancreas, Diabetes mellitus type 2, Permanent neonatal diabetes mellitus, Gastric ulcer, Hyperglycemia, Maturity-onset diabetes of the young (mody), Maturity-onset diabetes of the young, Neonatal diabetes mellitus, Pancreatic cancer, Pancreatic neoplasms, Partial pancreatic agenesis, Peptic ulcer disease

323
Pyridoxal dependent decarboxylase domain containing 1
LP8165
Renal cell carcinoma, Clonal hematopoiesis, Color vision deficiency, Insomnia, Metabolic syndrome, Schizophrenia, Diabetes mellitus type 2

324
Pyridoxal kinase
C21orf124, C21orf97, HEL-S-1a, HMSN6C, PKH, PNK, PRED79
Breast cancer, Coronary artery disease, Hypertension, Hereditary motor and sensory neuropathy, Status epilepticus

325
Prodynorphin
ADCA, PENKB, SCA23
Amnesia, Amphetamine or sympathomimetic abuse, Cerebellar ataxia, Bipolar disorder, Bradycardia, Cholelithiasis, Major depressive disorder, Dyskinesia, drug-induced, Dyskinesia, Temporal lobe epilepsy, Hyperalgesia, Hypercapnia, Hypotension, Hypoxia, Mood disorder
View all (7 more)

326
PDZ domain containing 2
AIPC, PAPIN, PDZK3, PIN1
Alzheimer disease, Bipolar disorder, Brain aneurysm, Central nervous system cancer, Asthma, Obstructive pulmonary disease, Color vision deficiency, Colorectal cancer, Dementia, Dental caries, Eye disease, Glaucoma, Glioblastoma, Glioma, Hearing loss
View all (7 more)

327
PDZ domain containing 4
LNX5, LU1, PDZK4, PDZRN4L
Autism, Intellectual developmental disorder, Movement disorder

328
PDZ domain containing 7
DFNB57, PDZK7
Congenital ear anomaly, Deafness, Hearing impairment, Hearing loss, Retinitis pigmentosa, Usher syndrome

329
PDZ domain containing 8
IDDADF, PDZK8
Alzheimer disease, Bipolar disorder, Intellectual developmental disorder autism dysmorphic, Major depressive disorder, Obsessive-compulsive disorder, Peripheral arterial disease, Schizophrenia

330
PDZ domain containing 9
C16orf65
Mitochondrial complex deficiency, Venous thromboembolism