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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 **7101 - 7125** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
2864	free fatty acid receptor 1	FFAR1	Homo sapiens (human)
389549	FEZ family zinc finger 1	FEZF1	Homo sapiens (human)
9637	fasciculation and elongation protein zeta 2	FEZ2	Homo sapiens (human)
26998	fetuin B	FETUB	Homo sapiens (human)
654463	fer-1 like family member 6	FER1L6	Homo sapiens (human)
90342	fer-1 like family member 5	FER1L5	Homo sapiens (human)
2237	flap structure-specific endonuclease 1	FEN1	Homo sapiens (human)
56929	fem-1 homolog C	FEM1C	Homo sapiens (human)
2232	ferredoxin reductase	FDXR	Homo sapiens (human)
2224	farnesyl diphosphate synthase	FDPS Aliases: farnesyl pyrophosphate synthetase, dimethylallyltranstransferase, geranyltranstransferase	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 Chagas disease Pick's disease Plasmodium falciparum malaria Reye syndrome Werner syndrome anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bone disease bone osteosarcoma brain cancer brain disease cancer cartilage disease cerebral degeneration chronic obstructive pulmonary disease colitis colon cancer colonic benign neoplasm congestive heart failure connective tissue disease coronary artery disease cutaneous leishmaniasis depressive disorder diabetes mellitus diabetic ketoacidosis dysthymic disorder embryoma gastroenteritis generalized anxiety disorder giant cell glioblastoma glioblastoma gonorrhea heart valve disease high grade glioma ileitis ileocolitis intestinal infectious disease leech infestation lymphoid leukemia major depressive disorder malignant fibrous histiocytoma melancholic depression melanoma microphthalmia multiple myeloma myeloid leukemia myiasis neurodegenerative disease neurotic disorder nutmeg liver obesity obsolete Matthew-Wood syndrome obsolete melancholia osteoporosis osteosarcoma pancreatic cancer pancreatic carcinoma phobic disorder photosensitive epilepsy photosensitivity disease pneumonia porokeratosis progeria prostate cancer prostate carcinoma pulmonary emphysema sickle cell anemia skin melanoma squamous cell carcinoma thyroid gland anaplastic carcinoma tongue squamous cell carcinoma toxoplasmosis trypanosomiasis type 2 diabetes mellitus
2222	farnesyl-diphosphate farnesyltransferase 1	FDFT1 Aliases: SQS squalene synthase	Homo sapiens (human)	Smith-Lemli-Opitz syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 acrodermatitis adenocarcinoma adenoma bronchus cancer bronchus carcinoma cancer cannabis abuse cannabis dependence cardiovascular system disease cataract chondrodysplasia punctata cocaine abuse cocaine dependence cribriform carcinoma dermatitis embryoma epilepsy familial hyperlipidemia familial mediterranean fever giant cell glioblastoma glioblastoma granular cell carcinoma heart disease hepatocellular carcinoma high grade glioma intellectual disability learning disability liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma melanoma mevalonic aciduria morbid obesity morphine dependence obesity phencyclidine abuse prostate cancer prostate carcinoma skin disease skin melanoma steatotic liver disease tubular adenocarcinoma visual cortex disease visual epilepsy
260436	follicular dendritic cell secreted protein	FDCSP	Homo sapiens (human)
197258	fucose kinase	FCSK Aliases: FLJ39408 L-fucose kinase	Homo sapiens (human)	congenital disorder of glycosylation congenital nystagmus dissociated nystagmus epilepsy esophagitis gastroesophageal reflux disease hypertropia intellectual disability learning disability mechanical strabismus ophthalmoplegia optic atrophy pathologic nystagmus peptic esophagitis spontaneous ocular nystagmus strabismus visual epilepsy
127943	Fc receptor like B	FCRLB	Homo sapiens (human)
84824	Fc receptor like A	FCRLA	Homo sapiens (human)
343413	Fc receptor like 6	FCRL6	Homo sapiens (human)
83416	Fc receptor like 5	FCRL5	Homo sapiens (human)
83417	Fc receptor like 4	FCRL4	Homo sapiens (human)
115352	Fc receptor like 3	FCRL3	Homo sapiens (human)
79368	Fc receptor like 2	FCRL2	Homo sapiens (human)
115350	Fc receptor like 1	FCRL1	Homo sapiens (human)
8547	ficolin 3	FCN3 Aliases: FCNH HAKA1 Hakata antigen	Homo sapiens (human)	Crohn's colitis Crohn's disease abdominal aortic aneurysm acute myocardial infarction amyotrophic lateral sclerosis anogenital venereal wart arteriosclerotic cardiovascular disease atherosclerosis bacterial infectious disease cancer 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 coronary artery disease coronary thrombosis diabetes mellitus essential hypertension gestational diabetes hepatocellular carcinoma hypertension inflammatory bowel disease 1 inflammatory bowel disease interstitial lung disease leprosy liver cancer lupus nephritis myocardial infarction ovarian cancer ovarian carcinoma placental insufficiency primary immunodeficiency disease progressive muscular atrophy sarcoidosis scleroderma silent myocardial infarction systemic lupus erythematosus systemic scleroderma tuberculosis type 2 diabetes mellitus type I complement component 8 deficiency type II complement component 8 deficiency ulcerative colitis
2220	ficolin 2	FCN2 Aliases: EBP-37 FCNL L-ficolin P35 collagen/fibrinogen domain-containing protein 2 ficolin B ficolin-2 hucolin serum lectin p35	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 adult acute lymphocytic leukemia B-cell lymphoma Behcet's disease Burkitt lymphoma Chagas disease Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Evans' syndrome Fleck corneal dystrophy Langerhans-cell histiocytosis Lyme disease Marfan syndrome Mycobacterium avium complex disease Niemann-Pick disease type C1 Niemann-Pick disease Pick's disease Reye syndrome St. Louis encephalitis Zollinger-Ellison syndrome acquired immunodeficiency syndrome acute myocardial infarction adenoiditis adult respiratory distress syndrome age related macular degeneration alternating hemiplegia of childhood amyloidosis amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 anaplastic astrocytoma anterior horn cell disease arteriosclerotic cardiovascular disease atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura autonomic neuropathy autosomal recessive distal hereditary motor neuronopathy 1 bacterial infectious disease bacterial sepsis benign mesothelioma bone osteosarcoma brain disease bronchiectasis bronchus cancer bronchus carcinoma cancer cataract 32 multiple types central nervous system disease cerebral degeneration cerebral infarction cerebrovascular disease childhood B-cell acute lymphoblastic leukemia childhood cerebral astrocytoma childhood osteosarcoma chromosome 17p13.1 deletion syndrome colorectal cancer colorectal carcinoma common variable immunodeficiency contagious pustular dermatitis coronary artery disease coronary thrombosis cowpox cutaneous leishmaniasis degeneration of macula and posterior pole dental caries dentin caries diabetic ketoacidosis embryoma enterobiasis erythema infectiosum exanthema subitum exudative vitreoretinopathy 1 exudative vitreoretinopathy fibrillary astrocytoma fissured tongue ganglioglioma gemistocytic astrocytoma geographic tongue gestational diabetes gingivitis glomerulonephritis heart disease hepatic veno-occlusive disease hepatitis B hepatitis C hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hyperinsulinism immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intellectual disability interstitial lung disease intestinal schistosomiasis juvenile pilocytic astrocytoma juvenile rheumatoid arthritis kidney disease large intestine cancer lateral sclerosis learning disability leishmaniasis leprosy lissencephaly liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung disease lupus erythematosus lupus nephritis lymphoma macular degeneration malaria malignant astrocytoma malignant mesothelioma microphthalmia milker's nodule motor neuron disease myocardial infarction myocarditis nephritis nervous system disease neuroblastoma neurodegenerative disease non-Hodgkin lymphoma obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma parapsoriasis pemphigus vulgaris pemphigus periodontitis pilocytic astrocytoma placental insufficiency pneumonia primary immunodeficiency disease progressive muscular atrophy prostate cancer prostate carcinoma protoplasmic astrocytoma psoriasis pulmonary tuberculosis pustulosis of palm and sole reticulosarcoma retinopathy of prematurity rheumatic fever rheumatoid arthritis rubella schistosomiasis schizophrenia scleroderma silent myocardial infarction situs inversus smallpox spinal muscular atrophy subependymal giant cell astrocytoma systemic lupus erythematosus systemic scleroderma temporal arteritis thyroid gland medullary carcinoma tongue disease tonsillitis trichinosis trypanosomiasis tuberculosis tuberculous pneumothorax tuberous sclerosis 1 tuberous sclerosis 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 ulcerative colitis urinary schistosomiasis variola major variola minor vascular disease viral infectious disease visceral leishmaniasis
2219	ficolin 1	FCN1 Aliases: FCNM	Homo sapiens (human)	Clostridium difficile colitis Kawasaki disease acute myocardial infarction arthritis arthropathy autoimmune disease autoimmune lymphoproliferative syndrome brain ischemia brain stem infarction cancer cerebral artery occlusion cerebral infarction cerebrovascular disease chronic fatigue syndrome colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis cystic fibrosis embryoma encephalomyelitis familial hyperlipidemia immune system disease large intestine cancer lepromatous leprosy leprosy lupus nephritis myocardial infarction perinatal necrotizing enterocolitis rheumatic fever rheumatoid arthritis silent myocardial infarction transient cerebral ischemia vasculitis vertebrobasilar insufficiency
9214	Fc mu receptor	FCMR	Homo sapiens (human)

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