Genes | GeDiPNet - Gene Disease Pathway & Associations

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10141 to 10150 of 15380 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
10141	55624	POMGNT1	Protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)	GNTI.2, GnT I.2, LGMD2O, LGMDR15, MEB, MGAT1.2, RP76, gnT-I.2	Autism, Limb girdle muscular dystrophy, Congenital muscular dystrophy due to dystroglycanopathy, Congenital muscular dystrophy, Congenital neurologic anomalies, Hydrocephalus, Intellectual developmental disorder, Limb-girdle muscular dystrophy, Lissencephaly, Macrogyria, Muscle eye brain disease, Muscular dystrophy, Optic atrophy, Retinitis pigmentosa, Walker-warburg syndrome
10142	84892	POMGNT2	Protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)	AGO61, C3orf39, GTDC2, MDDGA8, MDDGC8	Attention deficit hyperactivity disorder, Bipolar disorder, Insomnia, Major depressive disorder, Muscle eye brain disease, Obesity, Post-traumatic stress disorder, Schizophrenia, Substance abuse, Walker-warburg syndrome
10143	84197	POMK	Protein O-mannose kinase	MDDGA12, MDDGC12, SGK196	Congenital muscular dystrophy, Limb-girdle muscular dystrophy, Muscle eye brain disease, Walker-warburg syndrome
10144	51371	POMP	Proteasome maturation protein	C13orf12, HSPC014, PNAS-110, PRAAS2, UMP1	Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome, Proteasome associated autoinflammatory syndrome, Scoliosis
10145	10585	POMT1	Protein O-mannosyltransferase 1	LGMD2K, LGMDR11, MDDGA1, MDDGB1, MDDGC1, RT	Autism, Limb girdle muscular dystrophy, Cardiomyopathy, Cerebellar ataxia, Cleft lip, Complete unilateral cleft lip, Congenital muscular dystrophy, Congenital neurologic anomalies, Pyridoxine dependent epilepsy, Hearing impairment, Intellectual developmental disorder, Limb-girdle muscular dystrophy, Lissencephaly, Macrogyria, Muscle eye brain disease View all (3 more)
10146	29954	POMT2	Protein O-mannosyltransferase 2	LGMD2N, LGMDR14, MDDGA2, MDDGB2, MDDGC2	Autism, Limb girdle muscular dystrophy, Congenital muscular dystrophy, Intellectual developmental disorder, Limb-girdle muscular dystrophy, Lissencephaly, Macrogyria, Muscle eye brain disease, Muscular dystrophy, Walker-warburg syndrome
10147	5444	PON1	Paraoxonase 1	ESA, MVCD5, PON	Alzheimer disease, Amyotrophic lateral sclerosis, Anemia, Arteriosclerosis, Arteritis, Rheumatoid arthritis, Atherosclerosis, Eczema, Autism, Bipolar disorder, Brain neoplasms, Capillary leak syndrome, Cardiovascular disease, Cavernous malformations of cns, Ischemic stroke View all (49 more)
10148	5445	PON2	Paraoxonase 2	-	Alzheimer disease, Amyotrophic lateral sclerosis, Autism, Cardiovascular disease, Ischemic stroke, Ischemic heart disease, Coronary artery disease, Vascular dementia, Diabetes mellitus type 2, Hypercholesterolemia, Hyperlipoproteinemia, Myocardial ischemia
10149	5446	PON3	Paraoxonase 3	-	Alzheimer disease, Amyotrophic lateral sclerosis, Atherosclerosis, Autism
10150	10940	POP1	POP1 ribonuclease P/MRP subunit	ANXD2	Anauxetic dysplasia, Desbuquois syndrome, Prion disease

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