Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "P"
321 to 330 of 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

321
Decaprenyl diphosphate synthase subunit 1
COQ1, COQ10D2, COQ1A, DPS, SPS, TPRT, TPT, TPT 1, hDPS1
Coenzyme q10 deficiency, Color vision deficiency, Deafness, encephaloneuropathy, obesity, valvulopathy syndrome, Deafness-encephaloneuropathy-obesity-valvulopathy syndrome, Mitochondrial disease, Ovarian cancer, Ovarian serous carcinoma, Retinitis pigmentosa, Schizophrenia, Scoliosis

322
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

323
Pancreatic and duodenal homeobox 1
GSF, IDX-1, IPF1, IUF1, MODY4, PAGEN1, PDX-1, STF-1
Ischemic stroke, Congenital hypoplasia of pancreas, Experimental diabetes, Diabetes mellitus type 2, Diabetes mellitus permanent neonatal, Gastric ulcer, Hyperglycemia, Neonatal diabetes mellitus, Maturity-onset diabetes of the young (mody), Maturity-onset diabetes of the young, Pancreatic cancer, Pancreatic neoplasm, Partial pancreatic agenesis, Peptic ulcer disease, Diabetes mellitus, type 2

324
Pyridoxal dependent decarboxylase domain containing 1
LP8165
Renal cell carcinoma, Clonal hematopoiesis, Color vision deficiency, Insomnia, Metabolic syndrome, Schizophrenia, Diabetes mellitus, type 2

325
Pyridoxal kinase
C21orf124, C21orf97, HEL-S-1a, HMSN6C, PKH, PNK, PRED79
Breast cancer, Coronary artery disease, Hypertension, Hereditary motor and sensory neuropathy, Status epilepticus

326
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)

327
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)

328
PDZ domain containing 4
LNX5, LU1, PDZK4, PDZRN4L
Autism, Intellectual developmental disorder, Movement disorder

329
PDZ domain containing 7
DFNB57, PDZK7
Congenital ear anomaly, Deafness, Hearing impairment, Hearing loss, Retinitis pigmentosa, Usher syndrome

330
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