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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 **8776 - 8800** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
158724	family with sequence similarity 47 member A	FAM47A	Homo sapiens (human)
158763	Rho GTPase activating protein 36	ARHGAP36	Homo sapiens (human)
158809	MAGE family member B6	MAGEB6	Homo sapiens (human)
158866	zinc finger DHHC-type palmitoyltransferase 15	ZDHHC15	Homo sapiens (human)
158983	H2B.W histone 1	H2BW1	Homo sapiens (human)
159090	PABIR family member 2	PABIR2	Homo sapiens (human)
159163	RNA binding motif protein Y-linked family 1 member F	RBMY1F	Homo sapiens (human)
159195	ubiquitin specific peptidase 54	USP54	Homo sapiens (human)
159371	solute carrier family 35 member G1	SLC35G1 Aliases: C10orf60 FLJ33990 POST partner of STIM1	Homo sapiens (human)	Laron syndrome Werner syndrome acute myeloid leukemia agnosia arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis atrial fibrillation autistic disorder breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma coronary artery disease depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis dysthymic disorder embryoma epilepsy hemolytic-uremic syndrome hepatoblastoma hepatocellular carcinoma hyperglycemia intussusception kidney failure large intestine cancer leukemia major depressive disorder melancholic depression mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 neurotic disorder nutmeg liver obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 occipital horn syndrome polycystic ovary syndrome progeria prostate cancer prostate carcinoma schizophrenia sensorineural hearing loss transient myeloproliferative syndrome 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 uremia
159686	cilia and flagella associated protein 58	CFAP58	Homo sapiens (human)
159963	solute carrier family 5 member 12	SLC5A12	Homo sapiens (human)
160287	lactate dehydrogenase A like 6A	LDHAL6A Aliases: LDH6A MGC23940	Homo sapiens (human)	disease of metabolism
160335	transmembrane O-mannosyltransferase targeting cadherins 2	TMTC2 Aliases: DKFZp762A217	Homo sapiens (human)	allergic asthma asthma dermatitis glaucoma intrinsic asthma low tension glaucoma mutism primary open angle glaucoma sensorineural hearing loss
160364	C-type lectin domain family 12 member A	CLEC12A Aliases: CD371 CLL-1 DCAL-2 MICL dendritic cell-associated lectin 2 myeloid inhibitory C-type lectin-like receptor	Homo sapiens (human)	Crohn's colitis Crohn's disease Richter's syndrome acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia arthritis arthropathy cancer childhood leukemia chronic fatigue syndrome chronic lymphocytic leukemia chronic myeloid leukemia dermatophytosis embryoma encephalitis encephalomyelitis essential thrombocythemia fungal infectious disease immune system disease inflammatory bowel disease 1 inflammatory bowel disease leukemia lymphoblastic lymphoma lymphocytic choriomeningitis lymphoplasmacytic lymphoma macroglobulinemia monoclonal gammopathy of uncertain significance multiple myeloma multiple sclerosis myelitis myelodysplastic syndrome obsolete lymphoplasmacytic lymphoma rheumatoid arthritis ulcerative colitis
160418	transmembrane O-mannosyltransferase targeting cadherins 3	TMTC3 Aliases: FLJ90492 SMILE	Homo sapiens (human)	Joubert syndrome Miller-Dieker lissencephaly syndrome acute myocardial infarction adult lymphoma agranulocytosis aortic aneurysm aortic valve insufficiency blood coagulation disease breast cancer breast carcinoma cancerophobia central nervous system lymphoma childhood lymphoma complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congestive heart failure coronary thrombosis cortical dysplasia-focal epilepsy syndrome dental caries dentin caries dermoid cyst of ovary dermoid cyst enterocele epilepsy focal epilepsy hydranencephaly hydrocephalus intellectual disability learning disability leukopenia lissencephaly 8 lissencephaly lung cancer lung non-small cell carcinoma lymphoma myocardial infarction myopia neutropenia obsolete malignant histiocytosis obsolete ymphosarcoma optic atrophy partial motor epilepsy periventricular nodular heterotopia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 pyloric stenosis septooptic dysplasia severe congenital neutropenia short-rib thoracic dysplasia 14 with polydactyly silent myocardial infarction syndromic X-linked intellectual disability Najm type visual epilepsy
160492	lamin tail domain containing 1	LMNTD1	Homo sapiens (human)
160728	solute carrier family 5 member 8	SLC5A8	Homo sapiens (human)
160777	coiled-coil domain containing 60	CCDC60	Homo sapiens (human)
160851	diacylglycerol kinase eta	DGKH Aliases: DGKeta	Homo sapiens (human)	allergic asthma asthma attention deficit hyperactivity disorder bipolar disorder borderline personality disorder bronchus cancer bronchus carcinoma disease of mental health esophageal cancer esophageal carcinoma intermittent explosive disorder intrinsic asthma lung benign neoplasm lung cancer lung carcinoma melancholic depression mood disorder nephrolithiasis neurotic disorder obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia panic disorder psychotic disorder schizophrenia uric acid nephrolithiasis
160897	G protein-coupled receptor 180	GPR180	Homo sapiens (human)
161142	golgi associated RAB2 interactor family member 2	GARIN2	Homo sapiens (human)
161176	spectrin repeat containing nuclear envelope family member 3	SYNE3	Homo sapiens (human)
161198	C-type lectin domain containing 14A	CLEC14A	Homo sapiens (human)	IgA glomerulonephritis breast cancer cancer embryoma lung adenocarcinoma lung cancer melanoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma skin melanoma thymic carcinoma thymoma
161291	transmembrane protein 30B	TMEM30B	Homo sapiens (human)
161357	MAM domain containing glycosylphosphatidylinositol anchor 2	MDGA2	Homo sapiens (human)	Balo concentric sclerosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adrenoleukodystrophy benign epilepsy with centrotemporal spikes cancer central nervous system disease dissociative disorder embryoma microinvasive gastric cancer narcolepsy neurotic disorder rheumatoid arthritis sexual dysfunction stomach cancer stomach carcinoma systemic lupus erythematosus

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