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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	October 29, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **6876 - 6900** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
57662	calmodulin regulated spectrin associated protein family member 3	CAMSAP3	Homo sapiens (human)
79006	meteorin, glial cell differentiation regulator	METRN	Homo sapiens (human)
84146	zinc finger protein 644	ZNF644	Homo sapiens (human)
8398	phospholipase A2 group VI	PLA2G6 Aliases: NBIA2 PARK14 PNPLA9 iPLA2 iPLA2beta neurodegeneration with brain iron accumulation 2	Homo sapiens (human)	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 Behcet's disease Charcot-Marie-Tooth disease type 5 Crohn's colitis Crohn's disease DiGeorge syndrome Duchenne muscular dystrophy Glanzmann's thrombasthenia Graves' disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Henoch-Schoenlein purpura Lewy body dementia MASA syndrome Mast syndrome Parkinson's disease 14 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome SPOAN syndrome Stiff-Person syndrome Troyer syndrome Unverricht-Lundborg syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acute chest syndrome acute myocardial infarction adenocarcinoma adenoma adult respiratory distress syndrome agnosia alexia allergic asthma alternating hemiplegia of childhood amnestic disorder angiomatous meningioma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis autoimmune polyendocrine syndrome autonomic neuropathy autosomal dominant cerebellar ataxia basal ganglia disease benign meningioma bipolar disorder blepharospasm blindness brain disease breast cancer bronchitis bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease carotid artery disease central nervous system disease central retinal vein occlusion cerebellar ataxia cerebellar disease cerebral convexity meningioma cerebral degeneration cerebral infarction cerebrovascular disease cholestasis choreatic disease chronic fatigue syndrome chronic interstitial cystitis clear cell meningioma colitis colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma congenital nystagmus coronary artery disease coronary stenosis coronary thrombosis cribriform carcinoma cutaneous fibrous histiocytoma deficiency anemia delusional disorder dental caries dentin caries depressive disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus dyslexia dysthymic disorder dystonia 12 dystonia 16 dystonia early myoclonic encephalopathy embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma epilepsy familial adenomatous polyposis 1 familial adenomatous polyposis fibrous meningioma focal dystonia focal hand dystonia frontotemporal dementia gastroduodenal Crohn's disease gastroenteritis generalized dystonia granular cell carcinoma gray platelet syndrome heart disease hepatocellular carcinoma hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia hidradenoma hyperglycemia hypersensitivity vasculitis hyperthyroidism hypertropia hypochromic anemia ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome inflammatory bowel disease 1 inflammatory bowel disease interstitial cystitis intrahepatic cholestasis of pregnancy intraorbital meningioma intraventricular meningioma intrinsic asthma ischiocoxopodopatellar syndrome islet cell tumor isolated elevated serum creatine phosphokinase levels jejunoileitis keratitis keratoconjunctivitis large intestine cancer late onset Parkinson's disease leukodystrophy liver cancer liver carcinoma liver cirrhosis locked-in syndrome lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder mechanical strabismus melancholic depression melanoma membranous glomerulonephritis meningioma meningothelial meningioma microcystic meningioma microcytic anemia multiple sclerosis myelitis myocardial infarction nasopharynx carcinoma neovascular inflammatory vitreoretinopathy nervous system disease neuroaxonal dystrophy neuroblastoma neurodegeneration with brain iron accumulation 2a neurodegeneration with brain iron accumulation 2b neurodegeneration with brain iron accumulation 3 neurodegeneration with brain iron accumulation 4 neurodegeneration with brain iron accumulation 5 neurodegeneration with brain iron accumulation 6 neurodegeneration with brain iron accumulation neurodegenerative disease neurotic disorder newborn respiratory distress syndrome nicotine dependence nontoxic goiter nutmeg liver obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia obsolete type 1 diabetes mellitus 9 olfactory groove meningioma ophthalmoplegia optic atrophy optic neuritis pantothenate kinase-associated neurodegeneration papillary adenocarcinoma papillary renal cell carcinoma paranoid schizophrenia parasagittal meningioma pathologic nystagmus periventricular leukomalacia pituitary adenoma platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 pleurisy pneumonia pre-eclampsia prostate cancer prostate carcinoma psammomatous meningioma pseudosarcomatous fibromatosis quadriplegia qualitative platelet defect retinal disease retinitis retrograde amnesia sarcomatoid carcinoma schizophrenia secondary Parkinson disease secretory meningioma sensorineural hearing loss sickle cell anemia signet ring cell adenocarcinoma silent myocardial infarction skin melanoma skin papilloma skin tag spinal meningioma spontaneous ocular nystagmus steatotic liver disease strabismus syndromic X-linked intellectual disability type 10 syringoma temporal arteritis thrombophilia thyroid gland papillary carcinoma thyrotoxicosis transitional meningioma tubular adenocarcinoma 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 ulcerative colitis uterine corpus cancer velocardiofacial syndrome viral infectious disease visual epilepsy
159686	cilia and flagella associated protein 58	CFAP58	Homo sapiens (human)
116444	glutamate ionotropic receptor NMDA type subunit 3B	GRIN3B	Homo sapiens (human)
817	calcium/calmodulin dependent protein kinase II delta	CAMK2D	Homo sapiens (human)
5932	RB binding protein 8, endonuclease	RBBP8	Homo sapiens (human)
3674	integrin subunit alpha 2b	ITGA2B	Homo sapiens (human)
57501	cilia and flagella associated protein 92 (putative)	CFAP92	Homo sapiens (human)
23394	activity dependent neuroprotector homeobox	ADNP	Homo sapiens (human)
4887	neuropeptide Y receptor Y2	NPY2R	Homo sapiens (human)
10285	survival motor neuron domain containing 1	SMNDC1	Homo sapiens (human)
10188	tyrosine kinase non receptor 2	TNK2	Homo sapiens (human)
173	afamin	AFM	Homo sapiens (human)
89869	phospholipase C zeta 1	PLCZ1 Aliases: NYD-SP27 PLCzeta	Homo sapiens (human)	cystic fibrosis infertility ovarian cancer ovarian carcinoma spermatogenic failure 17
3118	major histocompatibility complex, class II, DQ alpha 2	HLA-DQA2	Homo sapiens (human)
6528	solute carrier family 5 member 5	SLC5A5	Homo sapiens (human)
64222	torsin family 3 member A	TOR3A	Homo sapiens (human)
83416	Fc receptor like 5	FCRL5	Homo sapiens (human)
2056	erythropoietin	EPO	Homo sapiens (human)
10867	tetraspanin 9	TSPAN9	Homo sapiens (human)
100133941	CD24 molecule	CD24	Homo sapiens (human)
5970	RELA proto-oncogene, NF-kB subunit	RELA	Homo sapiens (human)
81855	sideroflexin 3	SFXN3	Homo sapiens (human)

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