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 1361 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

831
Popeye domain cAMP effector 1
BVES, CARICK, HBVES, LGMD2X, LGMDR25, POP1
Atrial fibrillation, Limb girdle muscular dystrophy, Limb-girdle muscular dystrophy, Tetralogy of fallot

832
Popeye domain cAMP effector 3
LGMDR26, POP3, bA355M14.1
Atrial fibrillation, Limb girdle muscular dystrophy, Limb-girdle muscular dystrophy, Multiple sclerosis, Muscular dystrophy

833
Cytochrome p450 oxidoreductase
CPR, CYPOR, P450R
Ambiguous genitalia, Amenorrhea, Antley-bixler syndrome, Congenital adrenal hyperplasia, Congestive heart failure, Desbuquois syndrome, P450 oxidoreductase deficiency, Gliosarcoma, Heart failure, Hirschsprung disease, Learning disorders, Metabolic syndrome, Premature ovarian failure, Post-traumatic stress disorder, Diabetes mellitus type 2
View all (1 more)

834
Porcupine O-acyltransferase
DHOF, FODH, MG61, PORC, PPN
Anophthalmia/microphthalmia-esophageal atresia syndrome, Colobomatous microphthalmia, Focal dermal hypoplasia, Global developmental delay, Microphthalmia, Microphthalmos

835
Periostin
OSF-2, OSF2, PDLPOSTN, PN
Asthma, Attention deficit hyperactivity disorder, Bronchopulmonary dysplasia, Colorectal neoplasms, Liver cirrhosis, Substance abuse

836
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
View all (7 more)

837
POTE ankyrin domain family member C
A26B2, CT104.6, POTE-18, POTE18
Alzheimer disease

838
POU class 1 homeobox 1
CPHD1, GHF-1, PIT1, POU1F1a, Pit-1
Combined pituitary hormone deficiency, Desbuquois syndrome, Dwarfism, Hypothyroidism, Leber congenital amaurosis, Obsessive-compulsive disorder, Panhypopituitarism, Pituitary dwarfism, Pituitary hormone deficiency, Prostate cancer, Tourette syndrome

839
POU class 2 homeobox associating factor 1
BOB1, OBF-1, OBF1, OCAB
Agammaglobulinemia, Biliary cirrhosis, Colorectal cancer, Diverticular disease, Hodgkin lymphoma, Ovarian epithelial cancer, Multiple sclerosis, Nephrolithiasis, Ovarian cancer, Biliary cholangitis, Vascular dementia

840
POU class 2 homeobox associating factor 2
C11orf53, OCA-T1, OCAT1
Colorectal adenoma, Colorectal cancer