Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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9641 to 9650 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9641
PDS5 cohesin associated factor B
APRIN, AS3, CG008
Alzheimer disease, Asthma, Breast cancer, Coronary artery disease, Lung cancer, Metabolic syndrome, Myocardial infarction, Squamous cell carcinoma, Diabetes mellitus type 2, Upper aerodigestive tract neoplasm

9642
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

9643
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

9644
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

9645
Pyridoxal dependent decarboxylase domain containing 1
LP8165
Renal cell carcinoma, Clonal hematopoiesis, Color vision deficiency, Insomnia, Metabolic syndrome, Schizophrenia, Diabetes mellitus type 2

9646
Pyridoxal kinase
C21orf124, C21orf97, HEL-S-1a, HMSN6C, PKH, PNK, PRED79
Breast cancer, Coronary artery disease, Hypertension, Hereditary motor and sensory neuropathy, Status epilepticus

9647
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)

9648
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)

9649
PDZ domain containing 4
LNX5, LU1, PDZK4, PDZRN4L
Autism, Intellectual developmental disorder, Movement disorder

9650
PDZ domain containing 7
DFNB57, PDZK7
Congenital ear anomaly, Deafness, Hearing impairment, Hearing loss, Retinitis pigmentosa, Usher syndrome