GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

Genes (9988) Glycans (5831) Glycoproteins (15733) Lectins (298) Pathways (2074)

Displaying entries **6676 - 6700** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
132789	glucosamine-6-phosphate deaminase 2	GNPDA2 SB52 glucosamine-6-phosphate isomerase	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome abdominal obesity-metabolic syndrome 1 allergic asthma asthma cardiovascular system disease cerebral degeneration diabetes mellitus essential hypertension heart disease hypertension intrinsic asthma obesity type 2 diabetes mellitus
10007	glucosamine-6-phosphate deaminase 1	GNPDA1 GNPDA GPI HLN KIAA0060 glucosamine-6-phosphate deaminase oscillin
8443	glyceronephosphate O-acyltransferase	GNPAT DAP-AT DAPAT DHAPAT dihydroxyacetone phosphate acyltransferase glycerone-phosphate O-acyltransferase	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome Wilson disease X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 Zellweger syndrome attention deficit hyperactivity disorder autistic disorder autosomal dominant chondrodysplasia punctata cancer cataract cerebral degeneration chondrodysplasia punctata disease of mental health embryoma hemochromatosis type 1 hemochromatosis hepatocellular carcinoma intellectual disability iron metabolism disease learning disability liver cancer liver carcinoma liver cirrhosis microcephaly peroxisome biogenesis disorder 1A rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 rhizomelic chondrodysplasia punctata schizophrenia scoliosis
27232	glycine N-methyltransferase	GNMT	glycine N-methyltransferase deficiency hepatocellular carcinoma
26354	G protein nucleolar 3	GNL3
29889	G protein nucleolar 2	GNL2
2794	G protein nucleolar 1 (putative)	GNL1
10020	glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase	GNE Uae1 bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Bell's palsy GNE myopathy Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Paget's disease of bone Pick's disease Reye syndrome X-linked myopathy with excessive autophagy Zika fever amnestic disorder attention deficit hyperactivity disorder autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy cancer cardiomyopathy cerebral degeneration cholangiocarcinoma cholecystolithiasis choledocholithiasis cholelithiasis chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma congenital central hypoventilation syndrome congenital hypothyroidism dementia distal myopathy endomyocardial fibrosis epilepsy esophagitis facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis frontotemporal dementia gastroesophageal reflux disease hypertrophic cardiomyopathy hypothyroidism inclusion body myopathy with Paget disease of bone and frontotemporal dementia inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 inclusion body myositis inguinal hernia intrahepatic cholangiocarcinoma isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy mixed sleep apnea mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis muscular dystrophy myopathy myositis myxedema neuromuscular disease nonpapillary renal cell carcinoma obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obstructive sleep apnea oculopharyngeal muscular dystrophy pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peptic esophagitis renal carcinoma renal cell carcinoma retrograde amnesia sarcomatoid renal cell carcinoma scoliosis sialuria sleep apnea thrombocytopenia tibial muscular dystrophy visual epilepsy
59345	G protein subunit beta 4	GNB4
2782	G protein subunit beta 1	GNB1
346562	G protein subunit alpha transducin 3	GNAT3
2778	GNAS complex locus	GNAS
2773	G protein subunit alpha i3	GNAI3
2771	G protein subunit alpha i2	GNAI2
2770	G protein subunit alpha i1	GNAI1
10672	G protein subunit alpha 13	GNA13
8833	guanine monophosphate synthase	GMPS
29925	GDP-mannose pyrophosphorylase B	GMPPB KIAA1851 mannose-1-phosphate guanyltransferase beta	Bell's palsy Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Lambert-Eaton myasthenic syndrome Walker-Warburg syndrome agnosia amblyopia autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bilateral optic nerve hypoplasia blindness cardiomyopathy cataract centronuclear myopathy cleft palate clubfoot coloboma communicating hydrocephalus cone-rod dystrophy congenital muscular dystrophy-dystroglycanopathy A14 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy congenital myasthenic syndrome congenital nystagmus congenital ptosis congenital structural myopathy cryptorchidism developmental coordination disorder dissociated nystagmus distal myopathy endomyocardial fibrosis epilepsy esotropia facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis fundus albipunctatus glaucoma holoprosencephaly 1 holoprosencephaly hydrocephalus hypertrophic cardiomyopathy hypertropia idiopathic generalized epilepsy intellectual disability isolated cleft palate isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy mechanical strabismus megalocornea meningocele microcephaly microphthalmia monocular esotropia muscular dystrophy-dystroglycanopathy type B14 muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obstructive hydrocephalus oculopharyngeal muscular dystrophy oligohydramnios ophthalmoplegia optic atrophy pathologic nystagmus ptosis retinal detachment retinitis pigmentosa rippling muscle disease 2 scoliosis senile degeneration of brain sensorineural hearing loss speech disorder spontaneous ocular nystagmus strabismic amblyopia strabismus syndromic X-linked intellectual disability 94 visual epilepsy
29926	GDP-mannose pyrophosphorylase A	GMPPA	Addison's disease Down syndrome Laron syndrome achalasia achondroplasia adrenal cortical hypofunction alacrima, achalasia, and impaired intellectual development syndrome blindness coloboma epilepsy intellectual disability learning disability megaesophagus microcephaly nonepidermolytic palmoplantar keratoderma optic atrophy palmoplantar keratosis sensorineural hearing loss triple-A syndrome visual epilepsy
51053	geminin DNA replication inhibitor	GMNN
2765	glycosylphosphatidylinositol anchored molecule like	GML LY6DL	acute lymphoblastic leukemia cancer cardiovascular system disease colorectal cancer colorectal carcinoma congenital adrenal hyperplasia embryoma esophageal cancer esophageal carcinoma essential hypertension giant cell glioblastoma glioblastoma glucocorticoid-remediable aldosteronism heart disease high grade glioma hypertension large intestine cancer lung cancer lung non-small cell carcinoma lymphoblastic lymphoma lymphoid leukemia myeloid leukemia
26205	glucocorticoid modulatory element binding protein 2	GMEB2
10691	glucocorticoid modulatory element binding protein 1	GMEB1
2762	GDP-mannose 4,6-dehydratase	GMDS GMD SDR3E1 short chain dehydrogenase/reductase family 3E, member 1	agnosia arthritis arthropathy autistic disorder cancer cerebral palsy colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation type IIc embryoma hemiplegia hepatocellular carcinoma large intestine cancer liver cancer lung adenocarcinoma lung cancer open-angle glaucoma osteoarthritis primary open angle glaucoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy
2760	ganglioside GM2 activator	GM2A GM2-AP GM2-activator protein GM2AP SAP-3 cerebroside sulfate activator protein sphingolipid activator protein 3	Clostridium difficile colitis GM2 gangliosidosis, AB variant GM2 gangliosidosis Laron syndrome Sandhoff disease Schimke immuno-osseous dysplasia Tay-Sachs disease achondroplasia alcohol dependence alcohol use disorder anxiety disorder blindness breast cancer breast carcinoma cancer cerebral degeneration choreatic disease chronic obstructive pulmonary disease dementia dystonia embryoma epilepsy generalized anxiety disorder neurodegenerative disease neuroendocrine carcinoma nicotine dependence perinatal necrotizing enterocolitis progressive muscular atrophy retinal disease retinitis spinal muscular atrophy syndromic X-linked intellectual disability type 10 visual epilepsy vulvovaginal candidiasis