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
9711 to 9720 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

9711
Proline, glutamate and leucine rich protein 1
MNAR, P160
Global developmental delay, Psoriasis

9712
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

9713
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

9714
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, Venous thromboembolism

9715
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

9716
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

9717
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

9718
Proline and glutamate rich with coiled coil 1
DIAR11, ICR, gs104
Congenital epithelial dysplasia of intestine

9719
PPARGC1 and ESRR induced regulator, muscle 1
C1orf170
Atrial fibrillation

9720
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