GlyCosmos Portal

Homo sapiens (human)

Summary

Taxonomy ID: 9606
PubChem Taxonomy: 9606

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

Displaying entries **3276 - 3300** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
8001	glycine receptor alpha 3	GLRA3
2743	glycine receptor beta	GLRB
2745	glutaredoxin	GLRX
2744	glutaminase	GLS GAC GAM GLS1 K-glutaminase KGA KIAA0838 glutaminase C
144423	glycosyltransferase 1 domain containing 1	GLT1D1 FLJ31978	St. Louis encephalitis allergic asthma arteriosclerotic cardiovascular disease asthma atherosclerosis coronary artery disease intrinsic asthma
360203	glycosyltransferase 6 domain containing 1	GLT6D1	acute pericementitis aggressive periodontitis periodontitis periodontosis
55830	glycosyltransferase 8 domain containing 1	GLT8D1 AD-017 FLJ14611	amyotrophic lateral sclerosis anxiety disorder arthritis arthropathy bipolar disorder depressive disorder dysplastic nevus syndrome dysthymic disorder generalized anxiety disorder laryngostenosis major depressive disorder melancholic depression melanoma neurotic disorder obsolete melancholia osteoarthritis progressive muscular atrophy schizophrenia skin melanoma
83468	glycosyltransferase 8 domain containing 2	GLT8D2 FLJ31494	hepatitis C liver cirrhosis
51228	glycolipid transfer protein	GLTP	colon carcinoma colorectal cancer colorectal carcinoma hepatitis C large intestine cancer
2746	glutamate dehydrogenase 1	GLUD1
2747	glutamate dehydrogenase 2	GLUD2
2752	glutamate-ammonia ligase	GLUL glutamine synthetase	Addison's disease 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 Chagas disease Clostridium difficile colitis Graves' disease Griscelli syndrome type 2 Huntington's disease Lafora disease Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Stiff-Person syndrome Wernicke-Korsakoff syndrome Wilson disease acquired immunodeficiency syndrome acute monocytic leukemia acute myeloid leukemia adenocarcinoma adenoma adrenal cortical hypofunction adrenoleukodystrophy adult oligodendroglioma alcohol dependence alcohol use disorder alcoholic liver cirrhosis alternating hemiplegia of childhood amino acid metabolic disorder amnestic disorder amyotrophic lateral sclerosis arteriosclerotic cardiovascular disease atherosclerosis atrophic gastritis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thyroiditis autonomic neuropathy bacterial sepsis basal ganglia disease bile duct adenocarcinoma bile duct carcinoma bone osteosarcoma brain cancer brain disease brain stem infarction breast cancer breast carcinoma cancer cannabis abuse cannabis dependence carbamoyl phosphate synthetase I deficiency disease carcinoma cardiovascular system disease central nervous system cancer central nervous system disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease childhood oligodendroglioma childhood osteosarcoma cholangiocarcinoma chronic fatigue syndrome complex partial epilepsy congenital hypothyroidism coronary artery disease dental caries dentin caries depressive disorder dermatitis diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy disease of mental health disease of metabolism dysthymic disorder embryoma encephalitis encephalomyelitis epilepsy epithelioid sarcoma exanthem follicular adenoma giant cell glioblastoma glioblastoma gliosarcoma heart disease hemochromatosis hepatic coma hepatic encephalopathy hepatoblastoma hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hydrocephalus hyperglycemia hyperthyroidism hypothyroidism immune system disease intrahepatic cholangiocarcinoma iron metabolism disease irritable bowel syndrome lingual-facial-buccal dyskinesia liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung non-small cell carcinoma major depressive disorder melancholic depression microcystic adenoma microphthalmia middle cerebral artery infarction mixed glioma mixed oligodendroglioma-astrocytoma molybdenum cofactor deficiency type A mood disorder movement disease myelitis myopia myxedema nervous system disease neurocirculatory asthenia neurodegenerative disease neurotic disorder nutmeg liver obesity obsolete Matthew-Wood syndrome obsolete melancholia obsolete type 1 diabetes mellitus 9 oligodendroglioma ornithine carbamoyltransferase deficiency osteosarcoma pancreatic cancer pancreatic carcinoma pancreatic ductal carcinoma papillary adenoma placental insufficiency primary open angle glaucoma progressive muscular atrophy prostate cancer prostate carcinoma psychotic disorder purpura retinal disease retinitis retrograde amnesia sarcoma sarcomatoid carcinoma schizoaffective disorder schizophrenia schizophreniform disorder secondary Parkinson disease situs inversus spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spindle cell sarcoma steatotic liver disease stomach cancer stomach carcinoma temporal lobe epilepsy thyrotoxicosis transient cerebral ischemia trypanosomiasis tuberculosis tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus urea cycle disorder visual epilepsy
132158	glycerate kinase	GLYCTK HBEBP2 HBEBP4	D-glyceric aciduria Unverricht-Lundborg syndrome blepharospasm brain disease early myoclonic encephalopathy epilepsy focal hand dystonia glycine encephalopathy intellectual disability lactic acidosis learning disability locked-in syndrome microcephaly obsolete infantile epileptic encephalopathy primary hyperoxaluria quadriplegia schizophrenia visual epilepsy
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
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
10691	glucocorticoid modulatory element binding protein 1	GMEB1
26205	glucocorticoid modulatory element binding protein 2	GMEB2
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
51053	geminin DNA replication inhibitor	GMNN
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
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
8833	guanine monophosphate synthase	GMPS
10672	G protein subunit alpha 13	GNA13
2770	G protein subunit alpha i1	GNAI1
2771	G protein subunit alpha i2	GNAI2