Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10151 to 10160 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10151
POP4 ribonuclease P/MRP subunit
RPP29
Astrocytoma, Colorectal cancer, Diabetic retinopathy, Hypertension, Ovarian neoplasms

10152
POP7 ribonuclease P/MRP subunit
0610037N12Rik, RPP2, RPP20
Anemia, Autoimmune disease, Crohn disease, Hypothyroidism, Inflammatory bowel disease, Schizophrenia, Diabetes mellitus type 2, Ulcerative colitis

10153
Popeye domain cAMP effector 1
BVES, CARICK, HBVES, LGMD2X, LGMDR25, POP1
Atrial fibrillation, Limb girdle muscular dystrophy, Limb-girdle muscular dystrophy, Tetralogy of fallot

10154
Popeye domain cAMP effector 3
LGMDR26, POP3, bA355M14.1
Atrial fibrillation, Limb girdle muscular dystrophy, Limb-girdle muscular dystrophy, Multiple sclerosis, Muscular dystrophy

10155
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
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10156
Porcupine O-acyltransferase
DHOF, FODH, MG61, PORC, PPN
Anophthalmia/microphthalmia-esophageal atresia syndrome, Colobomatous microphthalmia, Focal dermal hypoplasia, Global developmental delay, Microphthalmia, Microphthalmos

10157
Periostin
OSF-2, OSF2, PDLPOSTN, PN
Asthma, Attention deficit hyperactivity disorder, Bronchopulmonary dysplasia, Colorectal neoplasms, Liver cirrhosis, Substance abuse

10158
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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10159
POTE ankyrin domain family member C
A26B2, CT104.6, POTE-18, POTE18
Alzheimer disease

10160
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