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"
831 to 840 of 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

831
Paraoxonase 3
-
Alzheimer disease, Amyotrophic lateral sclerosis, Atherosclerosis, Autism

832
POP1 ribonuclease P/MRP subunit
ANXD2
Anauxetic dysplasia, Desbuquois syndrome, Prion disease

833
POP4 ribonuclease P/MRP subunit
RPP29
Astrocytoma, Colorectal cancer, Diabetic retinopathy, Hypertension, Ovarian neoplasms

834
POP7 ribonuclease P/MRP subunit
0610037N12Rik, RPP2, RPP20
Anemia, Autoimmune disease, Crohn disease, Hypothyroidism, Inflammatory bowel disease, Schizophrenia, Diabetes mellitus type 2, Ulcerative colitis

835
Popeye domain cAMP effector 1
BVES, CARICK, HBVES, LGMD2X, LGMDR25, POP1
Atrial fibrillation, Limb girdle muscular dystrophy, Limb-girdle muscular dystrophy, Tetralogy of fallot

836
Popeye domain cAMP effector 3
LGMDR26, POP3, bA355M14.1
Atrial fibrillation, Limb girdle muscular dystrophy, Limb-girdle muscular dystrophy, Multiple sclerosis, Muscular dystrophy

837
Cytochrome p450 oxidoreductase
CPR, CYPOR, P450R
Ambiguous genitalia, Amenorrhea, Antley-bixler syndrome, Congenital adrenal hyperplasia, Congestive heart failure, Desbuquois syndrome, Disordered steroidogenesis due to cytochrome p450 oxidoreductase deficiency, Gliosarcoma, Heart failure, Hirschsprung disease, Learning disorders, Metabolic syndrome, Premature ovarian failure, Post-traumatic stress disorder, Diabetes mellitus type 2
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838
Porcupine O-acyltransferase
DHOF, FODH, MG61, PORC, PPN
Anophthalmia/microphthalmia-esophageal atresia syndrome, Colobomatous microphthalmia, Focal dermal hypoplasia, Global developmental delay, Microphthalmia, Microphthalmos

839
Periostin
OSF-2, OSF2, PDLPOSTN, PN
Asthma, Attention deficit hyperactivity disorder, Bronchopulmonary dysplasia, Colorectal neoplasms, Liver cirrhosis, Substance abuse

840
Protection of telomeres 1
CMM10, CRMCC3, GLM9, HPOT1, PFBMFT8, TPDS3
Anaplastic oligodendroglioma, Ankylosing spondylitis, B-cell chronic lymphocytic leukemia, Cerebroretinal microangiopathy with calcifications and cysts, Lymphocytic leukemia, Congenital chromosomal disease, Melanoma, Dyskeratosis congenita, Glioma, Hoyeraal hreidarsson syndrome, Kidney cancer, Lewy body disease, Lung cancer, Oligodendroglioma, Post-traumatic stress disorder
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