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
9371 to 9380 of 15435 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9371
Pyrimidinergic receptor P2Y6
P2Y6
Lung cancer, Squamous cell carcinoma

9372
Prolyl 3-hydroxylase 1
GROS1, LEPRE1, OI8
Bone fragility with contractures, arterial rupture, and deafness, Desbuquois syndrome, Osteogenesis imperfecta, Osteoporosis-pseudoglioma syndrome

9373
Prolyl 3-hydroxylase 2
LEPREL1, MCVD, MLAT4
Breast cancer, Congenital heart septal defect, Marshall syndrome, Myopia, Osteoarthritis, Psoriasis, Psoriasis vulgaris, Psychiatric disorders, Retinitis pigmentosa, Urinary bladder cancer

9374
Prolyl 3-hydroxylase 3
GRCB, HSU47926, LEPREL2
Osteoarthritis, Pancreatic cancer

9375
P3R3URF-PIK3R3 readthrough
LOC110117498-PIK3R3
Breast cancer, Hearing loss, Lung cancer, Diabetes mellitus type 2

9376
Prolyl 4-hydroxylase subunit alpha 1
P4HA
Atrial fibrillation, Bone fragility with contractures, arterial rupture, and deafness, Larsen syndrome, Osteoporosis-pseudoglioma syndrome

9377
Prolyl 4-hydroxylase subunit alpha 2
MYP25, lncRNA-PE
Asthma, Eczema, Basal cell carcinoma, Cardiovascular disease, Coronary artery disease, Crohn disease, Giant cell arteritis, Gout, Inflammatory bowel disease, Myopia, Retinitis pigmentosa, Ulcerative colitis, Vasculitis

9378
Prolyl 4-hydroxylase subunit alpha 3
-
Alzheimer disease

9379
Prolyl 4-hydroxylase subunit beta
CLCRP1, DSI, ERBA2L, GIT, P4Hbeta, PDI, PDIA1, PHDB, PO4DB, PO4HB, PROHB
Bone fragility with contractures, arterial rupture, and deafness, Cole-carpenter syndrome, Desbuquois syndrome, Heart disease, Myocardial ischemia, Osteogenesis imperfecta, Osteoporosis, Osteoporosis-pseudoglioma syndrome, Prostatic neoplasms, Spinocerebellar ataxia

9380
Prolyl 4-hydroxylase, transmembrane
EGLN4, HIDEA, HIFPH4, P4H-TM, PH-4, PH4, PHD4
Intellectual developmental disorder, Intellectual disability