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"
351 to 360 of 1361 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

351
Peptidase D
PROLIDASE
Androgenetic alopecia, Cataract, Skin ulcer, Prolidase deficiency, Diabetes mellitus type 2, Gestational diabetes, Hepatomegaly, Hypertension, Metabolic syndrome, Psoriasis, Schizophrenia, Splenomegaly, Venous thromboembolism

352
Period circadian regulator 1
PER, RIGUI, hPER
Juvenile arthritis, Autism, Generalized epilepsy, Iga nephropathy, Juvenile idiopathic arthritis, Major depressive disorder, Oligodendroglioma, Oligoarticular juvenile idiopathic arthritis, Substance abuse, Hypertension

353
Period circadian regulator 2
FASPS, FASPS1
Advanced sleep phase syndrome, Bipolar disorder, Major depressive disorder, Advanced sleep-phase syndrome, Insomnia, Irritable bowel syndrome, Multiple sclerosis, Substance abuse

354
Period circadian regulator 3
FASPS3, GIG13
Advanced sleep phase syndrome, Bipolar disorder, Breast neoplasms, Crohn disease, Bipolar depression, Major depressive disorder, Advanced sleep-phase syndrome, Homocystinuria with megaloblastic anemia, Inflammatory bowel disease, Osteoarthritis, Seasonal affective disorder, Substance abuse

355
Proline and glutamate rich with coiled coil 1
DIAR11, ICR, gs104
Congenital epithelial dysplasia of intestine

356
PPARGC1 and ESRR induced regulator, muscle 1
C1orf170
Atrial fibrillation

357
P53 apoptosis effector related to PMP22
EKVP7, KCP1, KRTCAP1, OLMS2, PIGPC1, THW, dJ496H19.1
Bulimia, Congenital palmoplantar and perioral keratoderma of olmsted, Erythrokeratodermia variabilis, Greither disease, Olmsted syndrome

358
Pescadillo ribosomal biogenesis factor 1
NOP7, PES
Cholangiocarcinoma, Dementia, Schizophrenia

359
PET100 cytochrome c oxidase chaperone
C19orf79, MC4DN12
Congenital lactic acidosis, Cytochrome c oxidase deficiency, Leigh syndrome, Mitochondrial complex deficiency

360
PET117 cytochrome c oxidase chaperone
CSRP2BP, MC4DN19
Cytochrome c oxidase deficiency, Leigh syndrome, Mitochondrial complex deficiency