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"
551 to 560 of 1361 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

551
Pipecolic acid and sarcosine oxidase
LPIPOX
Bipolar disorder, Gout, Major depressive disorder, Oligodendroglioma, Peroxisomal disorder

552
Pirin
-
Neurodevelopmental disorder, Contact dermatitis, Non-specific syndromic intellectual disability

553
Phosphatidylserine decarboxylase
DJ858B16, LIBF, PSD, PSDC, PSSC, dJ858B16.2
Lymphocytic leukemia, Desbuquois syndrome, Short stature skeletal dysplasia retinal degeneration intellectual disability hearing loss syndrome

554
Phosphatidylinositol transfer protein beta
PI-TP-beta, PtdInsTP, VIB1B
Breast cancer, Insomnia, Mitral valve prolapse, Oligodendroglioma, Osteoarthritis, Ovarian cancer, Ovarian serous carcinoma

555
Phosphatidylinositol transfer protein cytoplasmic 1
M-RDGB-beta, MRDGBbeta, RDGB-BETA, RDGBB, RDGBB1
Alzheimer disease, Asthma, Atrial fibrillation, Central serous retinopathy, Duodenal ulcer, Schizophrenia, Diabetes mellitus type 2

556
Phosphatidylinositol transfer protein membrane associated 1
DRES9, NIR2, PITPNM, RDGB, RDGB1, RDGBA, RDGBA1, Rd9
Schizophrenia

557
Phosphatidylinositol transfer protein membrane associated 2
NIR-3, NIR3, RDGB2, RDGBA2
Alzheimer disease, Asthma, Attention deficit hyperactivity disorder, Color vision deficiency, Insomnia, Multiple sclerosis, Obesity, Osteoarthritis, Parkinson disease, Schizophrenia, Tourette syndrome, Diabetes mellitus type 2, Uterine fibroid

558
PITPNM family member 3
ACKR6, CORD5, NIR1, RDGBA3
Cerebral arteriovenous malformations, Attention deficit hyperactivity disorder, Hepatocellular carcinoma, Cone dystrophy, Cone-rod dystrophy, Metabolic syndrome, Retinitis pigmentosa, Substance abuse, Diabetes mellitus type 2

559
Pitrilysin metallopeptidase 1
MP1, PreP, SCAR30
Cerebellar ataxia, Spinocerebellar ataxia

560
Paired like homeodomain 1
BFT, CCF, LBNBG, POTX, PTX1
Atrial fibrillation, Autism, Brachydactyly-elbow wrist dysplasia syndrome, Hepatocellular carcinoma, Clubfoot, Congenital clubfoot, Desbuquois syndrome, Micrognathism, Pfaundler-hurler syndrome, Testicular carcinoma, Testicular germ cell tumor