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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 **9601 - 9625** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
816	calcium/calmodulin dependent protein kinase II beta	CAMK2B	Homo sapiens (human)
815	calcium/calmodulin dependent protein kinase II alpha	CAMK2A	Homo sapiens (human)
814	calcium/calmodulin dependent protein kinase IV	CAMK4	Homo sapiens (human)
813	calumenin	CALU	Homo sapiens (human)
811	calreticulin	CALR Aliases: CRT FLJ26680 RO SSA Sicca syndrome antigen A (autoantigen Ro; calreticulin) autoantigen Ro cC1qR calregulin	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 Barrett's esophagus Behcet's disease Budd-Chiari syndrome Burkitt lymphoma Chagas disease Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Kuhnt-Junius degeneration Lyme disease Meckel syndrome Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Patau syndrome Pick's disease Reye syndrome Richter's syndrome Sjogren's syndrome St. Louis encephalitis T-cell acute lymphoblastic leukemia Weissenbacher-Zweymuller syndrome Wilson disease abdominal obesity-metabolic syndrome 1 achalasia acquired von Willebrand syndrome acrodermatitis acromegaly actinic keratosis acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adenosarcoma adenosquamous carcinoma adult lymphoma adult medulloblastoma age related macular degeneration aggressive systemic mastocytosis ampulla of Vater benign neoplasm amyotrophic lateral sclerosis anaplastic astrocytoma anemia anthrax disease antiphospholipid syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation atrioventricular block autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant polycystic kidney disease bacterial infectious disease bacterial sepsis benign ependymoma benign mesothelioma bipolar disorder bladder carcinoma bone inflammation disease bone marrow cancer bone osteosarcoma breast cancer breast carcinoma bronchiectasis bronchus cancer bronchus carcinoma bulimia nervosa cancer carcinoma cardiac arrest cardiac sarcoidosis cardiomyopathy cardiovascular system disease cat-scratch disease catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia cavernous hemangioma cellular ependymoma central nervous system cancer central nervous system lymphoma cerebral creatine deficiency syndrome 1 cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma cervix uteri carcinoma in situ childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood disintegrative disease childhood ependymoma childhood leukemia childhood medulloblastoma childhood osteosarcoma cholangiocarcinoma chorioangioma chromophobe renal cell carcinoma chronic lymphocytic leukemia chronic myeloid leukemia chronic neutrophilic leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart complement component 2 deficiency complement component 4a deficiency complement component 4b deficiency complement component 6 deficiency complement component 7 deficiency complement component 9 deficiency complement deficiency congenital heart block congenital secretory sodium diarrhea 3 congenital secretory sodium diarrhea 8 congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma cyclic hematopoiesis cystic fibrosis cystoid macular edema dedifferentiated liposarcoma degeneration of macula and posterior pole delusional disorder dental caries dentin caries depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma drug psychosis dysthymic disorder eclampsia embryoma endocarditis endometrial cancer endometrial carcinoma endomyocardial fibrosis enthesopathy esophageal cancer esophageal carcinoma esophagitis esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia familial adenomatous polyposis 1 familial adenomatous polyposis familial hypertrophic cardiomyopathy familial nephrotic syndrome fibrillary astrocytoma fibromyalgia follicular adenoma gallbladder cancer gastroenteritis gastroesophageal reflux disease gastrointestinal system cancer gemistocytic astrocytoma germ cell cancer germinoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glomus tumor glycogen storage disease II glycoproteinosis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease heart valve disease hemangioma hematologic cancer hematopoietic system disease hemochromatosis type 1 hemochromatosis hepatitis A hepatitis B hepatitis hepatocellular carcinoma high grade glioma histiocytoid hemangioma hyperpituitarism hypertension hyperthyroidism hypertrophic cardiomyopathy hypopharynx cancer ileitis ileocolitis immune system disease inclusion conjunctivitis indolent systemic mastocytosis inflammatory bowel disease intellectual disability intermittent claudication intrahepatic cholangiocarcinoma intramuscular hemangioma iron metabolism disease islet cell tumor juvenile myelomonocytic leukemia juvenile pilocytic astrocytoma keratoconjunctivitis sicca kidney disease kwashiorkor large intestine cancer laryngeal disease learning disability left bundle branch hemiblock leukemia lichen disease lipoid nephrosis liposarcoma liver cancer liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lung small cell carcinoma lupus erythematosus lupus nephritis lymphangioma lymphoma macrocytic anemia macular degeneration macular retinal edema major depressive disorder malignant astrocytoma malignant mesothelioma marasmus mastocytosis medulloblastoma medullomyoblastoma megaesophagus melancholic depression melanoma melanotic medulloblastoma melioidosis microcystic adenoma microphthalmia mixed glioma mucolipidosis II alpha/beta myelodysplastic syndrome myelofibrosis myeloproliferative neoplasm myocardial infarction myxopapillary ependymoma nasopharynx carcinoma nephritis nephroblastoma nephrosis nephrotic syndrome neuroblastoma neuroendocrine carcinoma neuroendocrine tumor neurotic disorder nonpapillary renal cell carcinoma nutrition disease obesity obsolete Matthew-Wood syndrome obsolete melancholia obsolete ymphosarcoma oculocutaneous albinism type IA oculocutaneous albinism onchocerciasis oral squamous cell carcinoma oral submucous fibrosis osteoarthritis osteosarcoma ovarian cancer ovarian carcinoma ovary serous adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatic ductal carcinoma pancytopenia papillary adenoma papillary ependymoma papillary renal cell carcinoma papilloma paranoid schizophrenia parotitis peptic esophagitis periodontitis peripheral vascular disease piebaldism pilocytic astrocytoma pineal region germinoma placental insufficiency plasmacytoma pleomorphic liposarcoma pneumonia polycythemia vera polycythemia portal hypertension post-traumatic stress disorder pre-eclampsia primary immunodeficiency disease proctitis progressive muscular atrophy prostate adenocarcinoma prostate cancer prostate carcinoma protein-energy malnutrition protoplasmic astrocytoma psychotic disorder purpura pyoureter rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma retinal disease retinal vascular occlusion retinitis rheumatoid arthritis rosacea sarcoidosis sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder severe acute respiratory syndrome sialadenitis sick sinus syndrome sideroblastic anemia silent myocardial infarction skin melanoma speech disorder spinal muscular atrophy squamous cell carcinoma squamous cell papilloma stomach cancer stomach carcinoma subependymal giant cell astrocytoma systemic lupus erythematosus systemic mastocytosis tanycytic ependymoma thrombocytosis thrombophilia thyroiditis thyrotoxicosis tongue cancer tongue squamous cell carcinoma tracheal disease transient cerebral ischemia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome trypanosomiasis tuberculosis tubular adenocarcinoma type 2 diabetes mellitus type I complement component 8 deficiency type II complement component 8 deficiency ureteral obstruction urinary bladder cancer uterine corpus cancer varicose veins vasculitis vertebrobasilar insufficiency viral infectious disease vitamin B12 deficiency vitiligo
800	caldesmon 1	CALD1	Homo sapiens (human)
799	calcitonin receptor	CALCR	Homo sapiens (human)
797	calcitonin related polypeptide beta	CALCB	Homo sapiens (human)
796	calcitonin related polypeptide alpha	CALCA	Homo sapiens (human)
793	calbindin 1	CALB1	Homo sapiens (human)
790	carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase	CAD Aliases: GATD4	Homo sapiens (human)
786	calcium voltage-gated channel auxiliary subunit gamma 1	CACNG1	Homo sapiens (human)
783	calcium voltage-gated channel auxiliary subunit beta 2	CACNB2	Homo sapiens (human)
782	calcium voltage-gated channel auxiliary subunit beta 1	CACNB1	Homo sapiens (human)
781	calcium voltage-gated channel auxiliary subunit alpha2delta 1	CACNA2D1 Aliases: alpha2delta-1 lncRNA-N3	Homo sapiens (human)	Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome West syndrome Williams-Beuren syndrome acute myeloid leukemia amelogenesis imperfecta type 1G atrial fibrillation atrioventricular block azoospermia brain infarction cancer cardiac arrest colon cancer colonic benign neoplasm colorectal cancer depressive disorder developmental and epileptic encephalopathy 110 embryoma epilepsy essential hypertension glaucoma hepatocellular carcinoma hypertension idiopathic scoliosis intellectual disability large intestine cancer learning disability liver cancer major depressive disorder malignant hyperthermia melancholic depression neurotic disorder obsolete infantile epileptic encephalopathy obsolete melancholia primary open angle glaucoma short QT syndrome sick sinus syndrome stomach cancer stomach carcinoma supravalvular aortic stenosis uveal melanoma
780	discoidin domain receptor tyrosine kinase 1	DDR1	Homo sapiens (human)
779	calcium voltage-gated channel subunit alpha1 S	CACNA1S	Homo sapiens (human)
778	calcium voltage-gated channel subunit alpha1 F	CACNA1F	Homo sapiens (human)
777	calcium voltage-gated channel subunit alpha1 E	CACNA1E	Homo sapiens (human)
776	calcium voltage-gated channel subunit alpha1 D	CACNA1D	Homo sapiens (human)
775	calcium voltage-gated channel subunit alpha1 C	CACNA1C	Homo sapiens (human)
774	calcium voltage-gated channel subunit alpha1 B	CACNA1B	Homo sapiens (human)
773	calcium voltage-gated channel subunit alpha1 A	CACNA1A	Homo sapiens (human)
771	carbonic anhydrase 12	CA12	Homo sapiens (human)
770	carbonic anhydrase 11	CA11	Homo sapiens (human)

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