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
10111 to 10120 of 15448 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

10111
Pancreatic lipase related protein 2 (gene/pseudogene)
PLRP2
Alzheimer disease, Coronary artery disease

10112
PNMA family member 1
MA1
Basal cell carcinoma

10113
PNMA family member 8A
PNMAL1
Colorectal cancer

10114
Phenylethanolamine N-methyltransferase
PENT, PNMTase
Alzheimer disease, Asthma, Cardiovascular disease, Heart failure, Hypertension, Multiple sclerosis, Pancreatic cancer

10115
Pinin, desmosome associated protein
DRS, DRSP, SDK3, memA
Insomnia

10116
Partner of NOB1 homolog
KHRBP1, RRP20
Hypertension

10117
Prepronociceptin
N/OFQ, NOP, OFQ, PPNOC, ppN/OFQ
Major depressive disorder, Hyperalgesia, Hypotension, Learning disorders, Memory disorders, Metabolic syndrome, Mood disorder, Parkinson disease, Substance abuse, Diabetes mellitus type 2

10118
Purine nucleoside phosphorylase
NP, PRO1837, PUNP
Alzheimer disease, Hearing loss, Osteoporosis, Severe combined immunodeficiency

10119
Patatin like domain 1, omega-hydroxyceramide transacylase
ARCI10, dJ50J22.1
Congenital ichthyosis, Congenital ichthyosiform erythroderma, Congenital nonbullous ichthyosiform erythroderma, Ichthyosis, Lamellar ichthyosis, Psychiatric disorders, Xeroderma

10120
Patatin like domain 2, triacylglycerol lipase
1110001C14Rik, ATGL, FP17548, PEDF-R, TTS-2.2, TTS2, iPLA2zeta
Congestive heart failure, Fuchs endothelial dystrophy, Heart disease, Heart failure, Hypertrophy, Keratoconus, Left ventricular disease, Myopathy, Nonalcoholic fatty liver disease, Polycystic ovary syndrome, Ventricular dysfunction