Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "P"
491 to 500 of 1361 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

491
Phosphatidylinositol binding clathrin assembly protein
CALM, CLTH, LAP
Alzheimer disease, Obstructive pulmonary disease, Cognition disorder, Dementia, Gastroesophageal reflux disease, Insomnia, Myeloid leukemia, Oligodendroglioma, Tourette syndrome

492
Protein interacting with PRKCA 1
PICK, PRKCABP
Amphetamine or sympathomimetic abuse, Male infertility globozoospermia, Male infertility round headed spermatozoa, Non-organic psychosis, Substance-induced psychosis, Psychotic disorders, Schizophrenia

493
Phosphotyrosine interaction domain containing 1
HMFN2073, NYGGF4, P-CLI1, PCLI1
Alzheimer disease, Carpal tunnel syndrome, Corneal neovascularization, Coronary artery disease, Dementia, Gastroesophageal reflux disease, Juvenile idiopathic arthritis, Keratitis, Moyamoya angiopathy, Myocardial infarction

494
P53-induced death domain protein 1
LRDD, MRT75, PIDD
Aortic stenosis, Aortic valve disease, Breast cancer, Renal cell carcinoma, Fuchs endothelial dystrophy, Intellectual developmental disorder, Keratoconus

495
Piezo type mechanosensitive ion channel component 1 (Er blood group)
DHS, ER, FAM38A, LMPH3, LMPHM6, Mib
Hemolytic anemia, Obstructive pulmonary disease, Hereditary xerocytosis, Diverticular disease, Hydrops fetalis, Non-immune hydrops fetalis, Lymphatic malformation, Osteoarthritis, Xerocytosis

496
Piezo type mechanosensitive ion channel component 2
C18orf30, C18orf58, DA3, DA5, DAIPT, FAM38B, FAM38B2, HsT748, HsT771, MWKS
Androgenetic alopecia, Arthrogryposis multiplex congenita, Arthrogryposis with oculomotor limitation and retinal anomalies, Distal arthrogryposis, Carotid artery disease, Central nervous system cancer, Cerebral palsy, Color vision deficiency, Congenital joint contractures, Connective tissue disease, Dental caries, Diverticular disease, Gorlin syndrome, Heterotaxy syndrome, Iga nephropathy
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497
Phosphatidylinositol glycan anchor biosynthesis class A
GPI3, MCAHS2, NEDEPH, PIG-A, PNH1
Cold paroxysmal hemoglobinuria, Neurodevelopmental disorder, Epilepsy of infancy with migrating focal seizures, Developmental and epileptic encephalopathy, Hemoglobinuria paroxysmal, Intellectual developmental disorder, Malignant migrating partial seizures of infancy, Non-specific syndromic intellectual disability, Occupational disease, Paroxysmal nocturnal hemoglobinuria, West syndrome

498
Phosphatidylinositol glycan anchor biosynthesis class B
DEE80, EIEE80, GPI-MT-III, PIG-B
Developmental and epileptic encephalopathy, Hyperphosphatasia with intellectual disability syndrome

499
Phosphatidylinositol glycan anchor biosynthesis class C
GPI2, GPIBD16, MRT62
Nonsyndromic intellectual disability, Global developmental delay, Glycosylphosphatidylinositol biosynthesis defect, Non-immune hydrops fetalis, Metabolic syndrome, Nonalcoholic fatty liver disease, Open angle glaucoma, Diabetes mellitus type 2

500
Phosphatidylinositol glycan anchor biosynthesis class G (EMM blood group)
EMM, GPI7, LAS21, MRT53, NEDHSCA, PRO4405, RLGS1930
Early-onset epilepsy-intellectual disability-brain anomalies syndrome, Hyperphosphatasia with intellectual disability syndrome, Intellectual developmental disorder, Neurodevelopmental disorder, Wolf-hirschhorn syndrome