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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 **8051 - 8075** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
93010	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7	B3GNT7 Aliases: beta3GnT7	Homo sapiens (human)	colon cancer colon carcinoma colonic benign neoplasm colorectal cancer large intestine cancer
93035	PKHD1 like 1	PKHD1L1	Homo sapiens (human)
93081	testis expressed 30	TEX30	Homo sapiens (human)
93099	dermokine	DMKN	Homo sapiens (human)
93109	transmembrane protein 44	TMEM44	Homo sapiens (human)
93129	ORAI calcium release-activated calcium modulator 3	ORAI3	Homo sapiens (human)
93134	zinc finger protein 561	ZNF561	Homo sapiens (human)
93145	olfactomedin 2	OLFM2	Homo sapiens (human)
93183	phosphatidylinositol glycan anchor biosynthesis class M	PIGM Aliases: DPM:GlcN-(acyl-)PI mannosyltransferase GPI mannosyltransferase 1 GPI-MT-I PIG-M dol-P-Man dependent GPI mannosyltransferase	Homo sapiens (human)	Budd-Chiari syndrome epilepsy focal epilepsy paroxysmal nocturnal hemoglobinuria partial motor epilepsy portal hypertension portal vein thrombosis thrombophilia visual epilepsy
93185	immunoglobulin superfamily member 8	IGSF8	Homo sapiens (human)
93210	post-GPI attachment to proteins phospholipase 3	PGAP3 Aliases: CAB2 MGC9753 PER1 PP1498 post-GPI attachment to proteins 3	Homo sapiens (human)	Cogan syndrome Crohn's colitis Crohn's disease Hirschsprung's disease Marfan syndrome Unverricht-Lundborg syndrome allergic asthma asthma bipolar disorder blepharospasm breast cancer breast carcinoma bruxism capillary disease congenital diaphragmatic hernia congenital disorder of glycosylation craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy epilepsy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia hyperphosphatasia with impaired intellectual development syndrome 4 inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intrinsic asthma isolated cleft palate learning disability lingual-facial-buccal dyskinesia monocular esotropia movement disease oligohydramnios scoliosis situs inversus stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 telangiectasis tuberous sclerosis ulcerative colitis visual epilepsy
93377	oligodendrocytic myelin paranodal and inner loop protein	OPALIN	Homo sapiens (human)
93380	membrane magnesium transporter 1	MMGT1	Homo sapiens (human)
93432	maltase-glucoamylase 2 (putative)	MGAM2	Homo sapiens (human)
93487	mitogen-activated protein kinase 1 interacting protein 1 like	MAPK1IP1L	Homo sapiens (human)
93589	calcium voltage-gated channel auxiliary subunit alpha2delta 4	CACNA2D4 Aliases: alpha2delta-4	Homo sapiens (human)	achromatopsia acquired color blindness acquired immunodeficiency syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness blue color blindness borderline personality disorder color blindness cone dystrophy cone-rod dystrophy 2 cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness disease of mental health dissociated nystagmus eye disease human immunodeficiency virus infectious disease hypertropia intermittent explosive disorder mechanical strabismus night blindness obsolete asthenopia ophthalmoplegia pathologic nystagmus psychotic disorder red color blindness red-green color blindness retinal cone dystrophy 4 spontaneous ocular nystagmus strabismus
93611	F-box protein 44	FBXO44 Aliases: FBG3 FBX30 Fbx44 Fbxo6a MGC14140	Homo sapiens (human)	polycystic ovary syndrome prostate cancer prostate carcinoma
93650	acid phosphatase 4	ACP4 Aliases: testicular acid phosphatase	Homo sapiens (human)
93659	chorionic gonadotropin subunit beta 5	CGB5	Homo sapiens (human)
93661	capping actin protein of muscle Z-line subunit alpha 3	CAPZA3	Homo sapiens (human)
93953	germ cell nuclear acidic peptidase	GCNA	Homo sapiens (human)
93978	C-type lectin domain containing 6A	CLEC6A Aliases: dectin-2 hDECTIN-2	Homo sapiens (human)	Kawasaki disease acute myocardial infarction arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer candidiasis cholesteatoma coronary artery disease coronary thrombosis cryptococcosis cystic fibrosis dermatomycosis dermatophytosis embryoma fungal infectious disease myocardial infarction pneumocystosis pneumonia polyp of middle ear rheumatoid arthritis silent myocardial infarction superficial mycosis tinea favosa tuberculosis vasculitis
93986	forkhead box P2	FOXP2	Homo sapiens (human)
94005	phosphatidylinositol glycan anchor biosynthesis class S	PIGS Aliases: GPI transamidase component PIG-S GPI transamidase subunit PIG-S	Homo sapiens (human)	breast cancer cancer congenital nystagmus developmental and epileptic encephalopathy 95 dissociated nystagmus embryoma epilepsy fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome gingival hypertrophy gingival overgrowth hepatocellular carcinoma liver cancer microcephaly omphalocele pathologic nystagmus spontaneous ocular nystagmus umbilical hernia visual epilepsy
94015	tweety family member 2	TTYH2	Homo sapiens (human)

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