Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "P"

941 to 950 of 1361 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
941	55844	PPP2R2D	Protein phosphatase 2 regulatory subunit Bdelta	B55D, B55delta, MDS026	Amyotrophic lateral sclerosis, Attention deficit hyperactivity disorder, Autism
942	5523	PPP2R3A	Protein phosphatase 2 regulatory subunit B''alpha	PPP2R3, PR130, PR72	Alzheimer disease, Atrial fibrillation, Bipolar disorder, Coronary artery disease, Dyslexia, Heart failure, Metabolic syndrome, Myocardial infarction, Neurotic disorder, Schizophrenia, Diabetes mellitus type 2
943	55012	PPP2R3C	Protein phosphatase 2 regulatory subunit B''gamma	C14orf10, G4-1, G5pr, GDRM, MEGD, SPGF36	Alzheimer disease, Ankylosing spondylitis, Eczema, Crohn disease, Male infertility globozoospermia, Psoriasis, Sclerosing cholangitis, Spermatogenic failure, Ulcerative colitis, Xy gonadal dysgenesis syndrome
944	5525	PPP2R5A	Protein phosphatase 2 regulatory subunit B'alpha	B56A, B56alpha, PR61A	Emphysema, Macular telangiectasia
945	5526	PPP2R5B	Protein phosphatase 2 regulatory subunit B'beta	B56B, B56beta, PR61B	Oligodendroglioma
946	5527	PPP2R5C	Protein phosphatase 2 regulatory subunit B'gamma	B56G, B56gamma, HJS4, PR61G	Autism, Chromosomal instability, Neurodevelopmental disorder, Global developmental delay, Houge janssens syndrome, Intellectual developmental disorder, Lymphocytic b-cell leukemia, Metabolic syndrome, Non-specific syndromic intellectual disability, Willis-ekbom disease, Papillary thyroid cancer, Diabetes mellitus type 2, Vitiligo
947	5528	PPP2R5D	Protein phosphatase 2 regulatory subunit B'delta	B56D, B56delta, HJS1, MRD35	Neurodevelopmental disorder, Global developmental delay, Houge janssens syndrome, Intellectual developmental disorder, Intellectual developmental disorder growth behavioral, Intellectual developmental disorder macrocephaly hypotonia behavioral, Non-specific syndromic intellectual disability
948	5529	PPP2R5E	Protein phosphatase 2 regulatory subunit B'epsilon	B56E, B56epsilon	Bronchial disease, Bronchitis, Chromosomal instability, Gallbladder neoplasms, Schizophrenia, Scoliosis
949	5530	PPP3CA	Protein phosphatase 3 catalytic subunit alpha	ACCIID, CALN, CALNA, CALNA1, CCN1, CNA1, DEE91, IECEE, IECEE1, PPP2B	Anorexia nervosa, Appendicitis, Arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development, Nonsyndromic intellectual disability, Brain injuries, Epithelial ovarian carcinoma, Color vision deficiency, Craniosynostosis, Developmental and epileptic encephalopathy, Developmental disability, Eating disorder, Gastroesophageal reflux disease, Hepatolenticular degeneration, Hypertrophy, Insomnia View all (10 more)
950	5532	PPP3CB	Protein phosphatase 3 catalytic subunit beta	CALNA2, CALNB, CNA2, PP2Bbeta	Congenital stenosis of aortic valve, Hepatolenticular degeneration

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