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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 **6501 - 6525** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
55793	MINDY lysine 48 deubiquitinase 1	MINDY1	Homo sapiens (human)
55794	DEAD-box helicase 28	DDX28	Homo sapiens (human)
55799	calcium voltage-gated channel auxiliary subunit alpha2delta 3	CACNA2D3 Aliases: HSA272268 alpha2delta-3	Homo sapiens (human)	acute myeloid leukemia anemia breast cancer breast carcinoma cancer carcinoma central nervous system cancer deficiency anemia embryoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma gliosarcoma heart conduction disease high grade glioma hypochromic anemia lung squamous cell carcinoma macrocytic anemia microcytic anemia mixed glioma nasopharynx carcinoma nicotine dependence prostate cancer prostate carcinoma sarcomatoid carcinoma schizophrenia stomach cancer stomach carcinoma uterine corpus cancer
55800	sodium voltage-gated channel beta subunit 3	SCN3B	Homo sapiens (human)
55802	decapping mRNA 1A	DCP1A Aliases: HSA275986 SMAD4IP1 SMIF	Homo sapiens (human)
55808	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 1	ST6GALNAC1 Aliases: ST6GalNAcI	Homo sapiens (human)	acute myocardial infarction bladder carcinoma breast cancer cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary thrombosis embryoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma inflammatory bowel disease 1 inflammatory bowel disease large intestine cancer myocardial infarction ovarian cancer ovarian carcinoma schizophrenia silent myocardial infarction stomach cancer stomach carcinoma ulcerative colitis urinary bladder cancer uterine corpus cancer
55810	forkhead box J2	FOXJ2	Homo sapiens (human)
55811	adenylate cyclase 10	ADCY10	Homo sapiens (human)
55814	BDP1 general transcription factor IIIB subunit	BDP1	Homo sapiens (human)
55818	lysine demethylase 3A	KDM3A	Homo sapiens (human)
55819	ring finger protein 130	RNF130	Homo sapiens (human)
55823	VPS11 core subunit of CORVET and HOPS complexes	VPS11	Homo sapiens (human)
55825	peroxisomal trans-2-enoyl-CoA reductase	PECR	Homo sapiens (human)
55827	DDB1 and CUL4 associated factor 6	DCAF6	Homo sapiens (human)
55830	glycosyltransferase 8 domain containing 1	GLT8D1 Aliases: AD-017 FLJ14611	Homo sapiens (human)	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
55832	cullin associated and neddylation dissociated 1	CAND1	Homo sapiens (human)
55833	ubiquitin associated protein 2	UBAP2	Homo sapiens (human)
55841	WWC family member 3	WWC3	Homo sapiens (human)
55843	Rho GTPase activating protein 15	ARHGAP15	Homo sapiens (human)
55852	testis expressed 2	TEX2	Homo sapiens (human)
55858	transmembrane protein 165	TMEM165 Aliases: GDT1 SLC64A1 TMPT27 TPA regulated locus TPARL	Homo sapiens (human)	Camurati-Engelmann disease Laron syndrome Marfan syndrome X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 achondroplasia acoustic neuroma amelogenesis imperfecta hypomaturation type 2A2 amelogenesis imperfecta hypomaturation type 2A3 amelogenesis imperfecta hypomaturation type 2A4 amelogenesis imperfecta hypomaturation type 2A5 amelogenesis imperfecta type 1A amelogenesis imperfecta type 1B amelogenesis imperfecta type 1C amelogenesis imperfecta type 1E amelogenesis imperfecta type 1F amelogenesis imperfecta type 1G amelogenesis imperfecta type 1H amelogenesis imperfecta type 2A1 amelogenesis imperfecta type 3A amelogenesis imperfecta type 4 amelogenesis imperfecta cancer cellular schwannoma chondrodysplasia punctata congenital disorder of glycosylation type II congenital disorder of glycosylation type IIk congenital disorder of glycosylation dentin dysplasia dentinogenesis imperfecta embryoma hepatocellular carcinoma isolated elevated serum creatine phosphokinase levels liver cancer melanotic neurilemmoma meningioma neurilemmoma neurofibromatosis osteoporosis pituitary adenoma plexiform schwannoma scoliosis situs inversus tuberous sclerosis vestibular schwannomatosis
55862	ethylmalonyl-CoA decarboxylase 1	ECHDC1 Aliases: dJ351K20.2	Homo sapiens (human)	bladder carcinoma breast cancer breast carcinoma melanoma ovarian cancer ovarian carcinoma skin melanoma urinary bladder cancer
55867	solute carrier family 22 member 11	SLC22A11	Homo sapiens (human)
55870	ASH1 like histone lysine methyltransferase	ASH1L	Homo sapiens (human)
55872	PDZ binding kinase	PBK	Homo sapiens (human)

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