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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 **8326 - 8350** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
54658	UDP glucuronosyltransferase family 1 member A1	UGT1A1 Aliases: UGT1A	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 Carney complex Crigler-Najjar syndrome Crohn's colitis Crohn's disease Fabry disease Gaucher's disease Gilbert syndrome Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute kidney failure acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction acute pyelonephritis adenocarcinoma adenoma adult respiratory distress syndrome agranulocytosis allergic asthma alpha thalassemia-X-linked intellectual disability syndrome alpha thalassemia-intellectual disability syndrome type 1 alpha thalassemia amnestic disorder anemia arteriosclerotic cardiovascular disease asthma atherosclerosis autism spectrum disorder autistic disorder bacterial sepsis beta thalassemia biliary tract cancer bilirubin metabolic disorder bladder carcinoma brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest cardiovascular system disease cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease cervical squamous cell carcinoma cholecystolithiasis choledocholithiasis cholelithiasis cholestasis chromophobe renal cell carcinoma chronic myeloid leukemia chylomicron retention disease clear cell renal cell carcinoma collecting duct carcinoma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital diarrhea 6 congenital hemolytic anemia congestive heart failure contact dermatitis coronary artery disease coronary thrombosis cryptococcosis cystic fibrosis cystinuria denture stomatitis diabetes mellitus diabetic ketoacidosis diarrhea differentiated thyroid gland carcinoma duodenum cancer embryoma endometrial cancer endometrial carcinoma epilepsy epithelioid sarcoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension female reproductive organ cancer follicular adenoma galactosemia gallbladder disease gastrointestinal system cancer glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease head and neck cancer head and neck squamous cell carcinoma heart cancer heart disease hematopoietic system disease hemiplegia hemochromatosis type 1 hemochromatosis hemoglobin C disease hemoglobin D disease hemoglobin E disease hemoglobin H disease hemoglobinopathy hemolytic anemia hepatitis A hepatitis B hepatitis C hepatitis D hepatitis hepatocellular carcinoma hereditary spherocytosis human immunodeficiency virus infectious disease hyperinsulinism hypertension hyperthyroidism hypertrophic pyloric stenosis inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma kernicterus due to isoimmunization kernicterus kidney disease large intestine cancer laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer leukopenia lipid storage disease liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung oat cell carcinoma lung small cell carcinoma lymphoblastic lymphoma macrocytic anemia microcystic adenoma myeloid leukemia myocardial infarction neonatal jaundice nephrolithiasis neutropenia newborn respiratory distress syndrome nodular prostate nonpapillary renal cell carcinoma nutmeg liver obesity obsolete type 1 diabetes mellitus 9 occupational dermatitis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenoma papillary renal cell carcinoma peripheral artery disease prostate cancer prostate carcinoma prostatic adenoma rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma retrograde amnesia sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma seminoma sensorineural hearing loss severe congenital neutropenia sickle cell anemia silent myocardial infarction small intestine adenocarcinoma small intestine cancer small intestine carcinoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spindle cell sarcoma squamous cell carcinoma status epilepticus stomach cancer stomach carcinoma stomatitis testicular cancer testis seminoma thalassemia thrombocytopenia thyrotoxicosis tongue squamous cell carcinoma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberculosis 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 ulcerative colitis ulcerative stomatitis uric acid nephrolithiasis urinary bladder cancer uterine corpus cancer visual epilepsy xeroderma pigmentosum group D
940	CD28 molecule	CD28	Homo sapiens (human)
54716	solute carrier family 6 member 20	SLC6A20	Homo sapiens (human)
26687	olfactory receptor family 4 subfamily E member 1	OR4E1	Homo sapiens (human)
60682	small ArfGAP 1	SMAP1	Homo sapiens (human)
51806	calmodulin like 5	CALML5	Homo sapiens (human)
10548	transmembrane 9 superfamily member 1	TM9SF1	Homo sapiens (human)
7036	transferrin receptor 2	TFR2	Homo sapiens (human)
1559	cytochrome P450 family 2 subfamily C member 9	CYP2C9 Aliases: P450IIC9	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 B-cell lymphoma Balo concentric sclerosis Behcet's disease Budd-Chiari syndrome Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Kawasaki disease Langerhans-cell histiocytosis Laron syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome Schwartz-Jampel syndrome 1 Stevens-Johnson syndrome achondroplasia acoustic neuroma acute kidney failure acute myocardial infarction adenocarcinoma adenoma adrenoleukodystrophy agnosia agranulocytosis alternating hemiplegia of childhood ankylosing spondylitis antithrombin III deficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation autoimmune hepatitis autonomic neuropathy brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cannabis abuse cannabis dependence cardiomyopathy cardiovascular system disease central nervous system cancer central nervous system disease cerebral degeneration cerebral infarction cerebrovascular disease cholestasis chronic kidney disease chronic lymphocytic leukemia colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis diaphragm disease diarrhea disease of metabolism duodenum disease dysthymic disorder eclampsia embryoma endomyocardial fibrosis epilepsy esophageal cancer esophageal carcinoma esophageal disease esophagus squamous cell carcinoma essential hypertension essential tremor exanthem eye disease familial hyperlipidemia follicular adenoma gallbladder disease gastric ulcer gastritis gingival hypertrophy gingival overgrowth gliosarcoma glomerulonephritis head and neck cancer head and neck squamous cell carcinoma heart disease hepatitis A hepatitis C hepatitis hepatocellular carcinoma high grade glioma hyperglycemia hypertension hyperthyroidism hypertrophic cardiomyopathy hypoglycemia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease 1 inflammatory bowel disease interstitial nephritis kidney disease kidney failure kwashiorkor large intestine cancer leukopenia liver cancer liver carcinoma liver disease lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lymphoma major depressive disorder marasmus melancholic depression meningioma microcystic adenoma mixed glioma multiple epiphyseal dysplasia multiple myeloma multiple sclerosis myocardial infarction narcolepsy nephritis nephrosis nervous system disease neurotic disorder neutropenia non-Hodgkin lymphoma nutmeg liver nutrition disease obesity obsolete melancholia obsolete ymphosarcoma osteochondrodysplasia papillary adenoma patent ductus arteriosus peptic ulcer disease pituitary adenoma primary pulmonary hypertension protein C deficiency protein S deficiency protein-energy malnutrition pyelitis pyelonephritis pyoureter rabies renal infectious disease reticulosarcoma retinal disease retinitis schizophrenia scleroderma severe congenital neutropenia silent myocardial infarction stomach disease substance abuse substance-related disorder sudden infant death syndrome systemic scleroderma thrombophilia thyrotoxicosis tuberculosis type 2 diabetes mellitus ulcerative colitis urea cycle disorder urinary bladder cancer vascular disease vasculitis vitamin K deficiency bleeding warfarin resistance
147339	arkadia (RNF111) N-terminal like PKA signaling regulator 2N	ARK2N	Homo sapiens (human)
57045	twisted gastrulation BMP signaling modulator 1	TWSG1	Homo sapiens (human)
51050	peptidase inhibitor 15	PI15	Homo sapiens (human)
57451	teneurin transmembrane protein 2	TENM2	Homo sapiens (human)
27332	zinc finger protein 638	ZNF638	Homo sapiens (human)
10990	leukocyte immunoglobulin like receptor B5	LILRB5	Homo sapiens (human)
2877	glutathione peroxidase 2	GPX2 Aliases: GSHPX-GI selenoprotein GPX2	Homo sapiens (human)	46,XY sex reversal Barrett's esophagus Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease adenocarcinoma adenoma agenesis of the corpus callosum with peripheral neuropathy bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cervical adenocarcinoma cervical cancer cervix carcinoma colitis colon cancer colon carcinoma colonic benign neoplasm colorectal adenoma colorectal cancer colorectal carcinoma embryoma follicular adenoma gastroenteritis hepatitis C hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease intestinal benign neoplasm intestinal cancer large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung squamous cell carcinoma microcystic adenoma motor peripheral neuropathy nasopharynx carcinoma obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum pancreatic cancer pancreatic carcinoma papillary adenoma prostate cancer prostate carcinoma rectal benign neoplasm rectum adenocarcinoma rectum cancer sarcomatoid carcinoma stomach cancer stomach carcinoma transitional cell carcinoma ulcerative colitis urinary bladder cancer
83666	poly(ADP-ribose) polymerase family member 9	PARP9 Aliases: ARTD9 BAL BAL1	Homo sapiens (human)	B-cell lymphoma Bloch-Sulzberger syndrome Gilles de la Tourette syndrome Goodpasture syndrome Loeffler syndrome Richter's syndrome Takayasu's arteritis X-linked chronic granulomatous disease acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia adult acute lymphocytic leukemia adult lymphoma adult respiratory distress syndrome agranulocytosis alcohol dependence alcohol use disorder allergic asthma anorexia nervosa asthma autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bacterial infectious disease bipolar disorder brain disease breast cancer breast carcinoma bronchiectasis cancer central nervous system lymphoma childhood acute lymphocytic leukemia childhood lymphoma chronic granulomatous disease chronic lymphocytic leukemia chronic obstructive pulmonary disease complement deficiency cutaneous porphyria cystic fibrosis diffuse large B-cell lymphoma embryoma eosinophilic pneumonia epithelioid sarcoma erythropoietic protoporphyria extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue extrinsic allergic alveolitis farmer's lung gastric lymphoma giardiasis granulomatosis with polyangiitis hepatitis hepatocellular carcinoma heroin dependence hypereosinophilic syndrome hypomelanosis of Ito idiopathic interstitial pneumonia idiopathic pulmonary fibrosis influenza interstitial lung disease intrinsic asthma leukopenia liver cancer lung disease lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 morphine dependence neutropenia newborn respiratory distress syndrome obesity obsolete ymphosarcoma opiate dependence pneumocystosis pneumonia polyarteritis nodosa postinflammatory pulmonary fibrosis primary ciliary dyskinesia 1 primary ciliary dyskinesia prostate cancer prostate carcinoma pulmonary alveolar proteinosis pulmonary eosinophilia pulmonary fibrosis pulmonary sarcoidosis pulmonary tuberculosis red-green color blindness rheumatoid arthritis sarcoidosis sarcoma schizophrenia scleroderma severe congenital neutropenia spindle cell sarcoma substance abuse substance-related disorder systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic scleroderma tuberculosis tuberculous pneumothorax uveoparotid fever
84125	leucine rich repeats and IQ motif containing 1	LRRIQ1	Homo sapiens (human)
23186	REST corepressor 1	RCOR1	Homo sapiens (human)
23262	diphosphoinositol pentakisphosphate kinase 2	PPIP5K2	Homo sapiens (human)
84976	dispatched RND transporter family member 1	DISP1	Homo sapiens (human)
5028	purinergic receptor P2Y1	P2RY1	Homo sapiens (human)
51350	keratin 76	KRT76	Homo sapiens (human)
51603	methyltransferase 13, eEF1A N-terminus and K55	METTL13	Homo sapiens (human)
9024	BR serine/threonine kinase 2	BRSK2	Homo sapiens (human)

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