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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 **8126 - 8150** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
5139	phosphodiesterase 3A	PDE3A Aliases: CGI-PDE cGMP-inhibited 3',5'-cyclic phosphodiesterase A	Homo sapiens (human)
3718	Janus kinase 3	JAK3	Homo sapiens (human)
285093	receptor transporter protein 5 (putative)	RTP5	Homo sapiens (human)
9124	PDZ and LIM domain 1	PDLIM1	Homo sapiens (human)
23133	PHD finger protein 8	PHF8	Homo sapiens (human)
353238	peptidyl arginine deiminase 6	PADI6	Homo sapiens (human)
1277	collagen type I alpha 1 chain	COL1A1	Homo sapiens (human)
284383	olfactory receptor family 2 subfamily Z member 1	OR2Z1	Homo sapiens (human)
9188	DExD-box helicase 21	DDX21	Homo sapiens (human)
114836	SLAM family member 6	SLAMF6	Homo sapiens (human)
55355	Holliday junction recognition protein	HJURP	Homo sapiens (human)
339398	leucine rich repeat and Ig domain containing 4	LINGO4	Homo sapiens (human)
150372	NFAT activating protein with ITAM motif 1	NFAM1	Homo sapiens (human)
5019	3-oxoacid CoA-transferase 1	OXCT1 Aliases: SCOT Succinyl-CoA:3-ketoacid-CoA transferase	Homo sapiens (human)	arteriosclerotic cardiovascular disease atherosclerosis beta-ketothiolase deficiency cancer carbohydrate metabolic disorder central nervous system cancer coronary artery disease diabetes mellitus embryoma gliosarcoma hepatocellular carcinoma high grade glioma liver cancer localized scleroderma mixed glioma nutmeg liver obesity osteoporosis phenylketonuria reflex sympathetic dystrophy scleroderma sickle cell anemia systemic scleroderma type 2 diabetes mellitus
3184	heterogeneous nuclear ribonucleoprotein D	HNRNPD	Homo sapiens (human)
85439	stonin 2	STON2	Homo sapiens (human)
391013	phospholipase A2 group IIC	PLA2G2C	Homo sapiens (human)
2312	filaggrin	FLG	Homo sapiens (human)
22796	component of oligomeric golgi complex 2	COG2	Homo sapiens (human)	atrial fibrillation cardiovascular system disease congenital disorder of glycosylation type IIq congenital disorder of glycosylation coronary artery disease diabetes mellitus epilepsy familial hypercholesterolemia heart disease hypobetalipoproteinemia locked-in syndrome obsolete constipation quadriplegia rheumatoid arthritis stomach cancer stomach carcinoma type 2 diabetes mellitus visual epilepsy
90850	zinc finger protein 598, E3 ubiquitin ligase	ZNF598	Homo sapiens (human)
3588	interleukin 10 receptor subunit beta	IL10RB	Homo sapiens (human)
7373	collagen type XIV alpha 1 chain	COL14A1	Homo sapiens (human)
57591	myocardin related transcription factor A	MRTFA	Homo sapiens (human)
8085	lysine methyltransferase 2D	KMT2D	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

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