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
9811 to 9820 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9811
Protein inhibitor of activated STAT 4
PIAS-gamma, PIASY, Piasg, ZMIZ6
Metabolic syndrome, Rhabdomyolysis, Diabetes mellitus type 2

9812
Progesterone immunomodulatory binding factor 1
C13orf24, CEP90, JBTS33, PIBF
Ciliopathy, Congenital cerebral hernia, Dandy-walker syndrome, Emphysema, Aplasia of the vermis, Gout, Joubert syndrome

9813
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

9814
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

9815
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

9816
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

9817
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

9818
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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9819
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

9820
Phosphatidylinositol glycan anchor biosynthesis class B
DEE80, EIEE80, GPI-MT-III, PIG-B
Developmental and epileptic encephalopathy, Hyperphosphatasia with intellectual disability syndrome