Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10071 to 10080 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10071
Pinin, desmosome associated protein
DRS, DRSP, SDK3, memA
Insomnia

10072
Partner of NOB1 homolog
KHRBP1, RRP20
Hypertension

10073
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

10074
Purine nucleoside phosphorylase
NP, PRO1837, PUNP
Alzheimer disease, Hearing loss, Osteoporosis, Severe combined immunodeficiency

10075
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

10076
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

10077
Patatin like domain 3, 1-acylglycerol-3-phosphate O-acyltransferase
ADPN, C22orf20, iPLA(2)epsilon
Biliary tract cancer, Brain disease, Cholecystolithiasis, Ischemic heart disease, Liver cirrhosis, Coronary artery disease, Diabetes mellitus, Diabetes mellitus type 2, Diabetic eye disease, Diabetic retinopathy, Digestive system disease, Esophageal varices, Fatty liver, Fatty liver, alcoholic, Gallstones
View all (17 more)

10078
Patatin like domain 4, phospholipase and triacylglycerol lipase
DXS1283E, GS2, iPLA2eta
Cortical development malformation

10079
Patatin like domain 6, lysophospholipase
BNHS, LNMS, NTE, NTEMND, OMCS, SPG39, iPLA2delta, sws
Amyotrophic lateral sclerosis, Ataxia-hypogonadism-choroidal dystrophy syndrome, Spastic paraplegia, Boucher-neuhauser syndrome, Cerebellar ataxia, Cerebellar ataxia and hypogonadotropic hypogonadism, Cerebellar ataxia-hypogonadism, Cerebellar atrophy, Chorioretinal dystrophy, spinocerebellar ataxia, hypogonadotropic hypogonadism syndrome, Desbuquois syndrome, Dysarthria, Female infertility, Hypogonadotropic hypogonadism, Kallmann syndrome, Motor neuron disease
View all (12 more)

10080
Patatin like domain 7, lysophospholipase
C9orf111, NTE-R1, NTEL1
Alzheimer disease, Mulibrey nanism, Premature ovarian failure, Peripheral neuropathy, autosomal recessive, with or without impaired intellectual development