Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
9671 to 9680 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9671
Phosphatidylethanolamine N-methyltransferase
PEAMT, PEMPT, PEMT2, PLMT, PNMT
Alzheimer disease, Coronary artery disease, Insomnia, Large artery stroke, Liver cirrhosis, Nonalcoholic fatty liver disease, Schizophrenia, Stroke, Diabetes mellitus type 2

9672
Proenkephalin
PE, PENK-A
Amyotrophic lateral sclerosis, Cannabis abuse, Major depressive disorder, Dyskinesia, drug-induced, Motor neuron disease, Narcolepsy, Nervous system disease, Obesity, Prostatic neoplasms

9673
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

9674
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

9675
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

9676
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

9677
Proline and glutamate rich with coiled coil 1
DIAR11, ICR, gs104
Congenital epithelial dysplasia of intestine

9678
PPARGC1 and ESRR induced regulator, muscle 1
C1orf170
Atrial fibrillation

9679
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

9680
Pescadillo ribosomal biogenesis factor 1
NOP7, PES
Cholangiocarcinoma, Dementia, Schizophrenia