Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "P"
841 to 850 of 1032 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

841
Praja ring finger ubiquitin ligase 1
PRAJA1, RNF70
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Craniofrontonasal dysplasia, Major depressive disorder, Parkinson disease, Psychiatric disorders, Schizophrenia

842
Pyruvate kinase M1/2 pseudogene 1
-

843
Phosphorylase kinase catalytic subunit gamma 1 pseudogene 2
-

844
PIK3CD antisense RNA 1
C1orf200

845
Serine protease 56
MCOP6
Angle closure glaucoma, Eye disease, Glaucoma, Hyperopia, Microphthalmia, Microphthalmos, Myopia, Nanophthalmos

846
Phospholipid phosphatase related 2
LPPR2, PRG4
Myocardial infarction

847
Poly(ADP-ribose) polymerase family member 12
ARTD12, MST109, MSTP109, ZC3H1, ZC3HDC1
Coronary artery disease, Macular degeneration, Major depressive disorder, Myocardial infarction, Vitiligo

848
Purinergic receptor P2Y12
ADPG-R, BDPLT8, HORK3, P2T(AC), P2Y(12)R, P2Y(AC), P2Y(ADP), P2Y(cyc), P2Y12, SP1999
Asthma, Platelet-type bleeding disorder, Cerebrovascular disorder, Developmental disability, Diabetes mellitus type 2, Digestive system disease, Diverticular disease, Hemorrhage, Intellectual developmental disorder, Systemic lupus erythematosus, Myocardial infarction, Neurodevelopmental disorders, Peripheral arterial disease, Von willebrand disorder

849
Porcupine O-acyltransferase
DHOF, FODH, MG61, PORC, PPN
Anophthalmia/microphthalmia-esophageal atresia syndrome, Colobomatous microphthalmia, Focal dermal hypoplasia, Global developmental delay, Microphthalmia, Microphthalmos

850
Pleckstrin homology and RhoGEF domain containing G2
ARHGEF42, CLG, CTB-60E11.4, LDAMD
Epilepsy, Jarcho-levin syndrome