Genesⓘ

Dataset:
? Protein-coding genes with reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "P"
351 to 360 of 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

351
Proenkephalin
PE, PENK-A
Amyotrophic lateral sclerosis, Cannabis abuse, Major depressive disorder, Dyskinesia, drug-induced, Motor neuron disease, Narcolepsy, Nervous system disease, Obesity, Prostatic neoplasm

352
Peptidase D
PROLIDASE
Androgenetic alopecia, Cataract, Skin ulcer, Prolidase deficiency, Diabetes mellitus type 2, Gestational diabetes, Hepatomegaly, Hypertension, Metabolic syndrome, Psoriasis, Respiratory system infectious disease, Schizophrenia, Splenomegaly, Diabetes mellitus, type 2, Venous thromboembolism

353
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

354
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

355
Period circadian regulator 3
FASPS3, GIG13
Advanced sleep phase syndrome, Bipolar disorder, Breast neoplasm, Crohn disease, Bipolar depression, Major depressive disorder, Advanced sleep-phase syndrome, Homocystinuria with megaloblastic anemia, Inflammatory bowel disease, Osteoarthritis, Seasonal affective disorder, Substance abuse

356
Proline and glutamate rich with coiled coil 1
DIAR11, ICR, gs104
Congenital epithelial dysplasia of intestine

357
PPARGC1 and ESRR induced regulator, muscle 1
C1orf170
Atrial fibrillation

358
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

359
Pescadillo ribosomal biogenesis factor 1
NOP7, PES
Cholangiocarcinoma, Dementia, Schizophrenia

360
PET100 cytochrome c oxidase chaperone
C19orf79, MC4DN12
Congenital lactic acidosis, Cytochrome c oxidase deficiency, Leigh syndrome, Mitochondrial complex deficiency