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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 **226 - 250** of **423164** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▲
135152	beta-1,3-glucuronyltransferase 2	B3GAT2 Aliases: GlcAT-S galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 2 glucuronosyltransferase S	Homo sapiens (human)	Barrett's esophagus schizophrenia
115908	collagen triple helix repeat containing 1	CTHRC1	Homo sapiens (human)	Barrett's esophagus
17294	mesoderm specific transcript	Mest	Mus musculus (house mouse)	Barth syndrome
6557	solute carrier family 12 member 1	SLC12A1	Homo sapiens (human)	Bartter disease type 1 Bartter disease
20495	solute carrier family 12, member 1	Slc12a1	Mus musculus (house mouse)	Bartter disease type 1
56379	potassium inwardly-rectifying channel, subfamily J, member 1	Kcnj1	Mus musculus (house mouse)	Bartter disease type 2
3758	potassium inwardly rectifying channel subfamily J member 1	KCNJ1	Homo sapiens (human)	Bartter disease type 2
1188	chloride voltage-gated channel Kb	CLCNKB	Homo sapiens (human)	Bartter disease type 3 Bartter disease type 4b Gitelman syndrome hypertension
56365	chloride channel, voltage-sensitive Kb	Clcnkb	Mus musculus (house mouse)	Bartter disease type 3 Bartter disease
10916	MAGE family member D2	MAGED2	Homo sapiens (human)	Bartter disease type 5
14183	fibroblast growth factor receptor 2	Fgfr2	Mus musculus (house mouse)	Beare-Stevenson cutis gyrata syndrome Crouzon syndrome Pfeiffer syndrome acrocephalosyndactylia intestinal atresia
1756	dystrophin	DMD Aliases: BMD DXS142 DXS164 DXS206 DXS230 DXS239 DXS268 DXS269 DXS270 DXS272 muscular dystrophy, Duchenne and Becker types	Homo sapiens (human)	Becker muscular dystrophy Duchenne muscular dystrophy X-linked dilated cardiomyopathy cognitive disorder dilated cardiomyopathy intellectual disability
13405	dystrophin, muscular dystrophy	Dmd	Mus musculus (house mouse)	Becker muscular dystrophy Duchenne muscular dystrophy
20742	spectrin beta, non-erythrocytic 1	Sptbn1	Mus musculus (house mouse)	Beckwith-Wiedemann syndrome
7450	von Willebrand factor	VWF	Homo sapiens (human)	Behcet's disease Bernard-Soulier syndrome atrial fibrillation end stage renal disease essential thrombocythemia pulmonary hypertension von Willebrand's disease 1 von Willebrand's disease 2 von Willebrand's disease 3 von Willebrand's disease
64127	nucleotide binding oligomerization domain containing 2	NOD2	Homo sapiens (human)	Behcet's disease Blau syndrome Crohn's disease PFAPA syndrome asthma autoimmune disease breast cancer bronchiolitis obliterans chronic obstructive pulmonary disease colorectal adenocarcinoma coronary artery disease familial Mediterranean fever gastritis gastrointestinal carcinoma graft-versus-host disease intestinal disease larynx cancer leprosy lung cancer meningococcal meningitis ovarian cancer pulmonary sarcoidosis pulmonary tuberculosis relapsing-remitting multiple sclerosis rhinitis systemic lupus erythematosus
6556	solute carrier family 11 member 1	SLC11A1	Homo sapiens (human)	Behcet's disease Buruli ulcer disease Crohn's disease cutaneous leishmaniasis inflammatory bowel disease juvenile rheumatoid arthritis leprosy lymphoproliferative syndrome multiple sclerosis pulmonary tuberculosis rheumatoid arthritis sarcoidosis systemic lupus erythematosus systemic scleroderma tuberculosis type 1 diabetes mellitus ulcerative colitis urinary bladder cancer visceral leishmaniasis
1636	angiotensin I converting enzyme	ACE Aliases: ACE1 CD143 peptidyl-dipeptidase A	Homo sapiens (human)	Behcet's disease COVID-19 Coronavirus infectious disease Fabry disease IgA glomerulonephritis IgA vasculitis allergic disease anemia ankylosing spondylitis aspiration pneumonia asthma atrial fibrillation breast cancer cerebral infarction chronic obstructive pulmonary disease coronary artery disease diabetic retinopathy diastolic heart failure end stage renal disease familial Mediterranean fever gallbladder adenocarcinoma heart valve disease hepatitis A hepatocellular carcinoma hypertension leukemia liver cirrhosis lung cancer mitral valve disease mitral valve prolapse multiple myeloma myocardial infarction nephritis non-arteritic anterior ischemic optic neuropathy obstructive sleep apnea pneumonia polycythemia pre-eclampsia proteinuria sarcoidosis stomach cancer subacute sclerosing panencephalitis toxic shock syndrome type 1 diabetes mellitus type 2 diabetes mellitus
3106	major histocompatibility complex, class I, B	HLA-B	Homo sapiens (human)	Behcet's disease COVID-19 Cytomegalovirus retinitis Graves' disease Meniere's disease Stevens-Johnson syndrome Takayasu's arteritis acute retinal necrosis syndrome allergic asthma alopecia ankylosing spondylitis anterior uveitis asthma birdshot chorioretinopathy cerebral infarction cervical cancer colitis dermatitis diabetic retinopathy erythema nodosum human immunodeficiency virus infectious disease mitral valve prolapse occupational asthma otosclerosis reactive arthritis retinal vasculitis retinopathy of prematurity sarcoidosis sensorineural hearing loss severe acute respiratory syndrome spondyloarthropathy synovitis thrombophlebitis trachoma tuberculosis uveitis
7040	transforming growth factor beta 1	TGFB1	Homo sapiens (human)	Behcet's disease Camurati-Engelmann disease aphthous stomatitis aplastic anemia asthma atopic dermatitis berylliosis breast cancer chronic obstructive pulmonary disease colon adenocarcinoma cystic fibrosis eosinophilic esophagitis factor VIII deficiency inflammatory bowel disease lung disease multiple myeloma myocardial infarction osteochondrodysplasia pulmonary emphysema pulmonary fibrosis pulmonary hypertension pulmonary sarcoidosis renal cell carcinoma tracheal stenosis uveitis
149233	interleukin 23 receptor	IL23R	Homo sapiens (human)	Behcet's disease Crohn's disease Graves ophthalmopathy Graves' disease ankylosing spondylitis arthritis celiac disease inflammatory bowel disease 17 multiple sclerosis osteonecrosis psoriasis 7 psoriasis pulmonary hypertension rheumatoid arthritis rhinitis sarcoidosis systemic scleroderma ulcerative colitis uveitis
2214	Fc gamma receptor IIIa	FCGR3A	Homo sapiens (human)	Behcet's disease Crohn's disease IgA glomerulonephritis allergic disease allergic rhinitis anti-basement membrane glomerulonephritis arthritis asthma autoimmune thrombocytopenic purpura coronary artery disease epilepsy graft-versus-host disease human immunodeficiency virus infectious disease immunodeficiency 20 lupus nephritis lymphopenia lymphoplasmacytic lymphoma myelodysplastic syndrome myositis pneumonia polyneuropathy rheumatoid arthritis systemic lupus erythematosus temporal arteritis thrombocytopenia due to platelet alloimmunization
5243	ATP binding cassette subfamily B member 1	ABCB1	Homo sapiens (human)	Behcet's disease Crohn's disease acquired immunodeficiency syndrome acute lymphoblastic leukemia allergic rhinitis antisocial personality disorder cannabis dependence chronic myeloid leukemia colorectal adenocarcinoma cryoglobulinemia drug dependence epilepsy familial Mediterranean fever familial hyperlipidemia hepatocellular carcinoma heroin dependence human immunodeficiency virus infectious disease inflammatory bowel disease 13 invasive ductal carcinoma lung non-small cell carcinoma malaria opiate dependence osteonecrosis pulmonary tuberculosis renal cell carcinoma toxic encephalopathy type 2 diabetes mellitus ulcerative colitis
3673	integrin subunit alpha 2	ITGA2	Homo sapiens (human)	Behcet's disease Glanzmann's thrombasthenia arteriosclerosis diabetes mellitus diabetic retinopathy intermediate coronary syndrome iron deficiency anemia myocardial infarction retinal vein occlusion sensorineural hearing loss thrombocytopenia thrombosis type 2 diabetes mellitus von Willebrand's disease 1 von Willebrand's disease 2
1493	cytotoxic T-lymphocyte associated protein 4	CTLA4	Homo sapiens (human)	Behcet's disease Graves ophthalmopathy Graves' disease Sjogren's syndrome acute myeloid leukemia alopecia areata anti-basement membrane glomerulonephritis asthma atopic dermatitis autoimmune hemolytic anemia autoimmune hepatitis autoimmune thyroiditis basal cell carcinoma breast cancer celiac disease chronic obstructive pulmonary disease end stage renal disease graft-versus-host disease granulomatosis with polyangiitis hepatitis B hepatocellular carcinoma immunoglobulin alpha deficiency iridocyclitis kidney disease latent autoimmune diabetes in adults lupus nephritis melanoma monoclonal gammopathy of uncertain significance multiple myeloma multiple sclerosis myocardial infarction non-Hodgkin lymphoma primary biliary cholangitis primary immunodeficiency disease psoriasis renal cell carcinoma sarcoidosis squamous cell carcinoma systemic lupus erythematosus type 1 diabetes mellitus 12 type 1 diabetes mellitus urinary schistosomiasis vitiligo

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