Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
10081 to 10090 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10081
Patatin like domain 8, phospholipase A2
IPLA2-2, IPLA2G, MMLA, PNPLA-gamma, iPLA2gamma
Oligodendroglioma, Ovarian serous carcinoma

10082
Pyridoxamine 5'-phosphate oxidase
HEL-S-302, PDXPO
Distal hereditary motor neuropathy, Pyridoxamine 5'-phosphate oxidase deficiency, Schizophrenia, Status epilepticus

10083
Polyribonucleotide nucleotidyltransferase 1
COXPD13, DFNB70, OLD35, PNPASE, SCA25, old-35
Amyotrophic lateral sclerosis, Androgenetic alopecia, Autoimmune thyroid disease, Isolated sensorineural deafness, Nonsyndromic intellectual disability, Hepatocellular carcinoma, Obstructive pulmonary disease, Combined oxidative phosphorylation deficiency, Deafness, Visual system disorder, Diverticular disease, Eye disease, Eyelid disease, Glaucoma, Global developmental delay
View all (15 more)

10084
POC1 centriolar protein A
PIX2, SOFT, WDR51A
Bipolar disorder, Desbuquois syndrome, Glomerulonephritis, Nephrolithiasis, Pituitary dwarfism, Diabetes mellitus type 2

10085
POC1 centriolar protein B
CORD20, PIX1, TUWD12, WDR51B
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Cholecystolithiasis, Ciliopathy, Cone-rod dystrophy, Gallstones, Heart failure, Insomnia, Major depressive disorder, Metabolic syndrome, Myocardial infarction, Peptic ulcer disease, Retinitis pigmentosa, Schizophrenia
View all (2 more)

10086
POC1B-GALNT4 readthrough
GALNT4, GalNAc-T4
Cone-rod dystrophy, Metabolic syndrome, Schizophrenia, Diabetes mellitus type 2

10087
POC5 centriolar protein
C5orf37
Anorexia nervosa, Atrial fibrillation, Attention deficit hyperactivity disorder, Cancer, Coronary artery disease, Diabetes mellitus, Heart failure, Metabolic syndrome, Migraine, Obesity, Optic atrophy, Retinitis pigmentosa, Scoliosis, Stroke, Diabetes mellitus type 2

10088
Podocan like 1
SLRR5B
Lung cancer, Squamous cell carcinoma

10089
Podocalyxin like
Gp200, PC, PCLP, PCLP-1, PDX, PODXL1, gp135
Juvenile parkinsonism, Carotid artery disease, Hemorrhage, Hypertension, Nephrotic syndrome, Parkinson disease, Hereditary parkinson disease, Prostatic neoplasms, Thrombosis

10090
POF1B actin binding protein
POF, POF2B
Dyslexia, Premature ovarian failure