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
Showing genes starting with "P"
761 to 770 of 1361 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

761
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)

762
POC1 centriolar protein A
PIX2, SOFT, WDR51A
Bipolar disorder, Desbuquois syndrome, Glomerulonephritis, Nephrolithiasis, Pituitary dwarfism, Diabetes mellitus type 2

763
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)

764
POC1B-GALNT4 readthrough
GALNT4, GalNAc-T4
Cone-rod dystrophy, Metabolic syndrome, Schizophrenia, Diabetes mellitus type 2

765
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

766
Podocan like 1
SLRR5B
Lung cancer, Squamous cell carcinoma

767
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

768
POF1B actin binding protein
POF, POF2B
Dyslexia, Premature ovarian failure

769
Protein O-fucosyltransferase 1
DDD2, FUT12, O-FUT, O-Fuc-T, O-FucT-1, OFUCT1
Ankylosing spondylitis, Asthma, Obstructive pulmonary disease, Neurodevelopmental disorder, Congenital disorder of glycosylation, Crohn disease, Dowling degos disease, Inflammatory bowel disease, Insomnia, Non-specific syndromic intellectual disability, Psoriasis, Sclerosing cholangitis, Ulcerative colitis

770
Pogo transposable element derived with KRAB domain
BASS2, KRBOX2, LST003
Insomnia, Osteoarthritis, Post-traumatic stress disorder