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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 **6001 - 6025** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
9468	phosphate cytidylyltransferase 1B, choline	PCYT1B Aliases: CCT-beta CCTbeta CTB CTP:phosphocholine cytidylyltransferase-beta choline-phosphate cytidylyltransferase beta phosphorylcholine transferase beta	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 Clouston syndrome Leber congenital amaurosis 1 Pick's disease Reye syndrome adult respiratory distress syndrome allergic rhinitis amyotrophic lateral sclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis breast cancer breast carcinoma breast ductal carcinoma cancer cerebral degeneration cholera colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease diabetes mellitus diabetic ketoacidosis embryoma hepatocellular carcinoma inflammatory bowel disease 1 inflammatory bowel disease juvenile rheumatoid arthritis large intestine cancer liver cancer liver carcinoma newborn respiratory distress syndrome progressive muscular atrophy prostate cancer prostate carcinoma type 2 diabetes mellitus ulcerative colitis urinary tract obstruction vasomotor rhinitis
9466	interleukin 27 receptor subunit alpha	IL27RA	Homo sapiens (human)
9465	A-kinase anchoring protein 7	AKAP7	Homo sapiens (human)
9462	RAS protein activator like 2	RASAL2	Homo sapiens (human)
9459	Rac/Cdc42 guanine nucleotide exchange factor 6	ARHGEF6	Homo sapiens (human)
9455	homer scaffold protein 2	HOMER2	Homo sapiens (human)
9452	integral membrane protein 2A	ITM2A	Homo sapiens (human)
9451	eukaryotic translation initiation factor 2 alpha kinase 3	EIF2AK3	Homo sapiens (human)
9450	lymphocyte antigen 86	LY86	Homo sapiens (human)
9448	mitogen-activated protein kinase kinase kinase kinase 4	MAP4K4	Homo sapiens (human)
9446	glutathione S-transferase omega 1	GSTO1	Homo sapiens (human)	Alzheimer's disease Parkinson's disease alcohol use disorder
9445	integral membrane protein 2B	ITM2B	Homo sapiens (human)
9444	QKI, KH domain containing RNA binding	QKI	Homo sapiens (human)
9439	mediator complex subunit 23	MED23	Homo sapiens (human)
9437	natural cytotoxicity triggering receptor 1	NCR1	Homo sapiens (human)
9436	natural cytotoxicity triggering receptor 2	NCR2	Homo sapiens (human)
9435	carbohydrate sulfotransferase 2	CHST2 Aliases: C6ST	Homo sapiens (human)	amyotrophic lateral sclerosis bone osteosarcoma cancer extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue gastric lymphoma inflammatory bowel disease 1 inflammatory bowel disease osteosarcoma progressive muscular atrophy ulcerative colitis
9429	ATP binding cassette subfamily G member 2 (JR blood group)	ABCG2	Homo sapiens (human)
9427	endothelin converting enzyme like 1	ECEL1	Homo sapiens (human)
9425	chromodomain Y like	CDYL	Homo sapiens (human)
9424	potassium two pore domain channel subfamily K member 6	KCNK6	Homo sapiens (human)
9423	netrin 1	NTN1	Homo sapiens (human)
9420	cytochrome P450 family 7 subfamily B member 1	CYP7B1	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 Charcot-Marie-Tooth disease type 5 Henoch-Schoenlein purpura MASA syndrome Mast syndrome Pick's disease Reye syndrome SPOAN syndrome Troyer syndrome acquired immunodeficiency syndrome adenocarcinoma adenoma arthritis arthropathy autosomal recessive polycystic kidney disease blood coagulation disease breast cancer breast carcinoma cancer cataract cerebellar ataxia cerebellar disease cerebral degeneration cholestasis chronic obstructive pulmonary disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital bile acid synthesis defect 3 congenital bile acid synthesis defect congenital nystagmus cribriform carcinoma critical illness polyneuropathy depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism dissociated nystagmus embryoma gallbladder cancer gallbladder carcinoma gallbladder disease gastroenteritis granular cell carcinoma hepatitis 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 hypersensitivity vasculitis ileitis ileocolitis inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholestasis kwashiorkor large intestine cancer lipid metabolism disorder liver disease luminal breast carcinoma A major depressive disorder marasmus melancholic depression meningoencephalitis multiple sclerosis neurodegenerative disease neuropathy nutrition disease obsolete inherited blood coagulation disease obsolete melancholia obsolete steatorrhea optic atrophy osteoarthritis paraplegia pathologic nystagmus peripheral nervous system disease polycystic kidney disease 4 polyneuropathy prostate adenocarcinoma prostate cancer prostate carcinoma protein-energy malnutrition rheumatoid arthritis scoliosis sensorineural hearing loss spontaneous ocular nystagmus steatotic liver disease tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis
9415	fatty acid desaturase 2	FADS2 Aliases: D6D DES6 FADSD6 SLL0262 TU13 delta-6-desaturase	Homo sapiens (human)	Crohn's colitis Crohn's disease Fabry disease Wolman disease abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute myocardial infarction age related macular degeneration alcohol use disorder allergic asthma alopecia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atopic dermatitis atrial fibrillation attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bipolar I disorder bipolar disorder breast cancer breast carcinoma cancer cardiovascular system disease cerebral infarction cerebrovascular disease chronic kidney disease chylomicron retention disease colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism congestive heart failure coronary artery disease coronary thrombosis degeneration of macula and posterior pole depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy discrete subaortic stenosis embryoma giant cell glioblastoma glioblastoma glomerulonephritis heart disease hemochromatosis type 1 hemochromatosis hepatitis hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hypothyroidism inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma kidney disease kwashiorkor large intestine cancer laryngeal squamous cell carcinoma lipid metabolism disorder lipid storage disease liver cancer lung benign neoplasm lung carcinoma macular degeneration major depressive disorder marasmus melancholic depression myocardial infarction myxedema nephritis nephrosis neurotic disorder nutmeg liver nutrition disease obesity obsolete melancholia polycystic ovary syndrome progressive pseudorheumatoid arthropathy of childhood protein-energy malnutrition psoriatic arthritis pyoureter rheumatoid arthritis schizophrenia silent myocardial infarction skin disease steatotic liver disease stomach cancer stomach carcinoma type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis vitiligo
9414	tight junction protein 2	TJP2	Homo sapiens (human)

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