Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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9781 to 9790 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9781
Phosphoglucomutase 2 like 1
BM32A, NEDHFS, PMMLP
Neurodevelopmental disorder, Non-specific syndromic intellectual disability

9782
Phosphoglucomutase 3
AGM1, IMD23, PAGM, PGM 3
Immunodeficiency, Insomnia, Schizophrenia, Severe combined immunodeficiency

9783
Phosphoglucomutase 5
PGMRP
Juvenile arthritis, Juvenile idiopathic arthritis, Oligoarticular juvenile idiopathic arthritis

9784
Phosphoglycolate phosphatase
AUM, G3PP, PGPase
Atrial fibrillation, Bipolar disorder

9785
Pyroglutamyl-peptidase I
PAP-I, PGI, PGP, PGP-I, PGPI, Pcp
Alzheimer disease, Atrial fibrillation, Bipolar disorder, Cardiovascular disease, Coronary artery disease, Hypertension, Gastroesophageal reflux disease, Major depressive disorder, Metabolic syndrome, Schizophrenia, Systemic lupus erythematosus, Diabetes mellitus type 2

9786
Progesterone receptor
NR3C3, PR
Breast neoplasms, Carcinoma, Chiari-frommel syndrome, Diabetic neuropathy, Endometrial cancer, Endometrial neoplasms, Endometriosis, Heart failure, Hyperproinsulinemia, Hypertrophic cardiomyopathy, Meningioma, Mesothelioma, Obesity, Squamous cell carcinoma

9787
Progesterone receptor membrane component 1
Dap1, HPR6.6, IZA, MPR
Alzheimer disease, Congenital cataract, Congenital total cataract, Hodgkin lymphoma, Prostatic neoplasms, Cataract

9788
Progesterone receptor membrane component 2
DG6, PMBP
Central nervous system cancer, Glioblastoma, Glioma, Diabetes mellitus type 2

9789
Phosphatidylglycerophosphate synthase 1
-
Lipoprotein lipase deficiency, Metabolic syndrome, Parkinson disease, Myopia, Systemic lupus erythematosus, Diabetes mellitus type 2

9790
Phosphatase and actin regulator 1
DEE70, EIEE70, RPEL, RPEL1, dJ257A7.2
Atherosclerosis, Attention deficit hyperactivity disorder, Cardiovascular disease, Ischemic stroke, Cerebrovascular trauma, Ischemic heart disease, Color vision deficiency, Common migraine, Coronary artery disease, Coronary stenosis, Developmental and epileptic encephalopathy, Dilated cardiomyopathy, Hypertension, Heart disease, Heart failure
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