Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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9871 to 9880 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9871
Phosphatidylinositol-4-phosphate 5-kinase type 1 gamma
LCCS3, PIP5K-GAMMA, PIP5K1-gamma, PIP5Kgamma
Neurodevelopmental disorder, Lethal congenital contracture syndrome, Non-specific syndromic intellectual disability

9872
Phosphatidylinositol-4-phosphate 5-kinase like 1
PIPKH
Cataract, Gout

9873
Pipecolic acid and sarcosine oxidase
LPIPOX
Bipolar disorder, Gout, Major depressive disorder, Oligodendroglioma, Peroxisomal disorder

9874
Pirin
-
Neurodevelopmental disorder, Contact dermatitis, Non-specific syndromic intellectual disability

9875
Phosphatidylserine decarboxylase
DJ858B16, LIBF, PSD, PSDC, PSSC, dJ858B16.2
Lymphocytic leukemia, Desbuquois syndrome, Short stature skeletal dysplasia retinal degeneration intellectual disability hearing loss syndrome

9876
Phosphatidylinositol transfer protein beta
PI-TP-beta, PtdInsTP, VIB1B
Breast cancer, Insomnia, Mitral valve prolapse, Oligodendroglioma, Osteoarthritis, Ovarian cancer, Ovarian serous carcinoma

9877
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

9878
Phosphatidylinositol transfer protein membrane associated 1
DRES9, NIR2, PITPNM, RDGB, RDGB1, RDGBA, RDGBA1, Rd9
Schizophrenia

9879
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

9880
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