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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 **7976 - 8000** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
4543	melatonin receptor 1A	MTNR1A	Homo sapiens (human)
4540	NADH dehydrogenase subunit 5	ND5	Homo sapiens (human)
4537	NADH dehydrogenase subunit 3	ND3	Homo sapiens (human)
4534	myotubularin 1	MTM1	Homo sapiens (human)	Bell's palsy 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 2 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 4 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 IgA glomerulonephritis Poland syndrome X-linked dilated cardiomyopathy abdominal obesity-metabolic syndrome 1 adult respiratory distress syndrome agenesis of the corpus callosum with peripheral neuropathy atrioventricular block autosomal dominant centronuclear myopathy autosomal recessive centronuclear myopathy breast cancer breast carcinoma cancer capillary hemangioma cavernous hemangioma centronuclear myopathy 1 centronuclear myopathy X-linked centronuclear myopathy chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer communicating hydrocephalus congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congenital myopathy 4A congenital ptosis congenital structural myopathy cryptorchidism cystinuria dental caries dentin caries diabetes mellitus diabetic ketoacidosis diaphragmatic eventration diarrhea dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy embryoma endocarditis epilepsy facial nerve disease facial paralysis familial periodic paralysis galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hemangioma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hydrocephalus infective endocarditis intrahepatic cholestasis large intestine cancer megaconial type congenital muscular dystrophy motor peripheral neuropathy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myofibrillar myopathy 1 myopathy myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 nemaline myopathy neurodegenerative disease neuromuscular disease neuropathy newborn respiratory distress syndrome obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obstructive hydrocephalus oculocerebrorenal syndrome ophthalmoplegia peripheral nervous system disease placental insufficiency polyhydramnios polyneuropathy ptosis pyloric stenosis rabies rigid spine muscular dystrophy 1 scoliosis senile degeneration of brain subacute bacterial endocarditis tubular aggregate myopathy 1 type 2 diabetes mellitus visual epilepsy
4522	methylenetetrahydrofolate dehydrogenase, cyclohydrolase and formyltetrahydrofolate synthetase 1	MTHFD1	Homo sapiens (human)
4520	metal regulatory transcription factor 1	MTF1	Homo sapiens (human)
4512	cytochrome c oxidase subunit I	COX1	Homo sapiens (human)
4507	methylthioadenosine phosphorylase	MTAP Aliases: MSAP S-methyl-5'-thioadenosine phosphorylase c86fus	Homo sapiens (human)	B-cell lymphoma Barrett's esophagus Ehlers-Danlos syndrome Ewing sarcoma Langerhans-cell histiocytosis Q fever Sezary's disease T-cell acute lymphoblastic leukemia X-linked ichthyosis acute lymphoblastic leukemia acute myocardial infarction acute pancreatitis adenocarcinoma adenoma adult T-cell leukemia/lymphoma adult acute lymphocytic leukemia adult fibrosarcoma adult lymphoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis benign deep fibrous histiocytoma benign mesothelioma benign pleural mesothelioma biliary tract benign neoplasm biliary tract cancer bone cancer bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer central nervous system lymphoma cerebral infarction cerebrovascular disease childhood T-cell acute lymphoblastic leukemia childhood acute lymphocytic leukemia childhood lymphoma childhood osteosarcoma chondrosarcoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon carcinoma colorectal cancer common bile duct neoplasm coronary artery disease coronary thrombosis cribriform carcinoma cutaneous fibrous histiocytoma diaphyseal medullary stenosis with malignant fibrous histiocytoma diffuse large B-cell lymphoma dysplastic nevus syndrome embryoma endometrial cancer endometrial carcinoma epithelioid sarcoma esophageal cancer esophageal carcinoma esophagus adenocarcinoma esophagus squamous cell carcinoma familial retinoblastoma fibrosarcoma follicular adenoma gallbladder disease gastric adenocarcinoma gastrointestinal stromal tumor giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hepatocellular carcinoma hidradenoma high grade glioma histiocytoma laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer liver cancer liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoblastic lymphoma lymphoid leukemia lymphoma malignant mesothelioma malignant pleural mesothelioma mantle cell lymphoma melanoma microcystic adenoma mixed glioma mycosis fungoides myeloid leukemia myocardial infarction nasopharynx carcinoma neuroblastoma neuroendocrine carcinoma neuroendocrine tumor neurofibromatosis nodular malignant melanoma non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver obsolete T-cell lymphoblastic leukemia/lymphoma obsolete ymphosarcoma oropharynx cancer osteogenesis imperfecta osteosarcoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis papillary adenoma papillary renal cell carcinoma periampullary adenocarcinoma peripheral T-cell lymphoma pleurisy primary cutaneous T-cell non-Hodgkin lymphoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma reticulohistiocytic granuloma reticulosarcoma retinoblastoma sarcoma sarcomatoid carcinoma sarcomatoid mesothelioma sarcomatoid renal cell carcinoma sclerosing hemangioma sensorineural hearing loss silent myocardial infarction skin benign neoplasm skin cancer skin melanoma skin papilloma skin tag sleeping sickness spindle cell sarcoma squamous cell carcinoma stomach cancer stomach carcinoma syringoma tongue squamous cell carcinoma trilateral retinoblastoma trypanosomiasis tubular adenocarcinoma typhus uterine corpus cancer vestibular schwannomatosis
4502	metallothionein 2A	MT2A	Homo sapiens (human)
4496	metallothionein 1H	MT1H	Homo sapiens (human)
4495	metallothionein 1G	MT1G	Homo sapiens (human)
4493	metallothionein 1E	MT1E	Homo sapiens (human)
4486	macrophage stimulating 1 receptor	MST1R	Homo sapiens (human)
4485	macrophage stimulating 1	MST1	Homo sapiens (human)
4482	methionine sulfoxide reductase A	MSRA	Homo sapiens (human)
4481	macrophage scavenger receptor 1	MSR1	Homo sapiens (human)
4478	moesin	MSN	Homo sapiens (human)
4440	musashi RNA binding protein 1	MSI1	Homo sapiens (human)
4438	mutS homolog 4	MSH4	Homo sapiens (human)
4436	mutS homolog 2	MSH2	Homo sapiens (human)
4430	myosin IB	MYO1B	Homo sapiens (human)
4363	ATP binding cassette subfamily C member 1 (ABCC1 blood group)	ABCC1 Aliases: GS-X glutathione S-conjugate export pump	Homo sapiens (human)
4361	MRE11 homolog, double strand break repair nuclease	MRE11	Homo sapiens (human)
4360	mannose receptor C-type 1	MRC1 Aliases: CD206 CLEC13D CLEC13DL bA541I19.1 macrophage mannose receptor	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 Behcet's disease CD40 ligand deficiency CREST syndrome Clouston syndrome Down syndrome Duchenne muscular dystrophy EEC syndrome Evans' syndrome Ewing sarcoma Fanconi anemia complementation group A Fanconi anemia Guillain-Barre syndrome Hantavirus hemorrhagic fever with renal syndrome 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 Japanese encephalitis Leigh disease Lynch syndrome Marfan syndrome Marinesco-Sjogren syndrome Miller Fisher syndrome Muir-Torre syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome Sjogren-Larsson syndrome Sveinsson chorioretinal atrophy T-cell acute lymphoblastic leukemia X-linked hyper IgM syndrome X-linked ichthyosis abdominal obesity-metabolic syndrome 1 acquired hyperkeratosis acquired immunodeficiency syndrome acrodermatitis actinic keratosis adenocarcinoma adenoma adenosarcoma adult T-cell leukemia/lymphoma adult lymphoma alcoholic hepatitis allergic asthma allergic contact dermatitis amyotrophic lateral sclerosis anaplastic astrocytoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy aseptic meningitis aspergillosis asthma atherosclerosis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura autosomal dominant pseudohypoaldosteronism type 1 autosomal recessive pseudohypoaldosteronism type 1 bacterial sepsis basal cell carcinoma benign giant cell tumor benign mesothelioma bile duct adenocarcinoma bile duct carcinoma bipolar disorder black piedra bladder carcinoma bladder urothelial carcinoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma bulbar polio bullous pemphigoid cancer carcinoma cardiovascular system disease central nervous system cancer central nervous system lymphoma cerebral degeneration cerebral infarction cerebral palsy cerebral primitive neuroectodermal tumor cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood cerebral astrocytoma childhood leukemia childhood lymphoma childhood testicular germ cell tumor childhood type dermatomyositis cholangiocarcinoma cholesteatoma choriocarcinoma chromophobe renal cell carcinoma chronic interstitial cystitis chronic lymphocytic leukemia chronic myeloid leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma clear cell sarcoma cleft palate coccidioidomycosis colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common variable immunodeficiency common wart complement deficiency congestive heart failure coronary artery disease craniosynostosis crescentic glomerulonephritis cribriform carcinoma cutaneous Paget's disease deafness-dystonia-optic neuronopathy syndrome dengue disease dermatitis dermatomyositis diabetes mellitus dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism distal arthrogryposis duodenum cancer dysplastic nevus syndrome ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 embryoma encephalitis encephalomyelitis endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometrial hyperplasia endometrioid ovary carcinoma endometriosis of uterus endometriosis epilepsy epithelioid leiomyosarcoma epithelioid sarcoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma exanthema subitum factor VIII deficiency fallopian tube cancer fallopian tube carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis female reproductive organ cancer fibrillary astrocytoma follicular adenoma gastroenteritis gastroparesis gemistocytic astrocytoma gestational trophoblastic neoplasm giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart cancer heart disease hematologic cancer hemiplegia hepatitis A hepatitis B hepatitis C hepatocellular carcinoma hereditary breast ovarian cancer syndrome herpes simplex high grade glioma histoplasmosis human immunodeficiency virus infectious disease hyper IgM syndrome idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune system disease immunodeficiency with hyper IgM type 3 in situ carcinoma inflammatory bowel disease influenza inherited metabolic disorder insulinoma interstitial cystitis interstitial lung disease intrahepatic cholangiocarcinoma intrinsic asthma islet cell tumor isolated cleft palate juvenile pilocytic astrocytoma keratoacanthoma kidney cancer large intestine cancer laryngeal disease leiomyosarcoma leishmaniasis leprosy leukemia liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung oat cell carcinoma lung small cell carcinoma lupus erythematosus lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 malignant astrocytoma malignant mesothelioma malignant teratoma mantle cell lymphoma mature teratoma measles medulloblastoma medulloepithelioma melanoma microcystic adenoma microphthalmia mixed glioma morbid obesity mucinous adenocarcinoma multiple myeloma mumps muscular dystrophy myelitis myositis myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 myxoid leiomyosarcoma nasopharynx carcinoma nephroblastoma neuroblastoma neurodegenerative disease neuroectodermal tumor neurofibromatosis 1 neurofibromatosis nodular prostate nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome obsolete T-cell lymphoblastic leukemia/lymphoma obsolete congenital ichthyosiform erythroderma obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete ymphosarcoma osteoarthritis ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma parapsoriasis pemphigus vulgaris pemphigus penis carcinoma in situ penis carcinoma periampullary adenocarcinoma pilocytic astrocytoma placenta cancer pneumocystosis pneumonia poliomyelitis polyp of middle ear postinflammatory pulmonary fibrosis primary cerebellar degeneration primary pulmonary hypertension progressive muscular atrophy prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma prune belly syndrome pseudohypoaldosteronism psoriasis pulmonary fibrosis pulmonary tuberculosis pustulosis of palm and sole rapidly progressive glomerulonephritis rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma rheumatoid arthritis rubella sarcoidosis sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma sebaceous gland neoplasm seminoma situs inversus skin benign neoplasm skin cancer skin carcinoma skin melanoma small intestine adenocarcinoma small intestine cancer small intestine carcinoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spindle cell sarcoma sporadic breast cancer sporotrichosis squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma superficial mycosis supratentorial primitive neuroectodermal tumor syndromic X-linked intellectual disability 94 systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic scleroderma tarsal-carpal coalition syndrome teratoma testicular cancer testicular germ cell cancer testis seminoma thrombocytopenia due to platelet alloimmunization thrombocytopenia thymus lymphoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma tracheal disease transitional cell carcinoma transthyretin amyloidosis trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberculosis tuberculous pneumothorax tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer uterine corpus cancer uveoparotid fever viral infectious disease viral meningitis visceral leishmaniasis visual epilepsy white piedra yellow fever
4359	myelin protein zero	MPZ	Homo sapiens (human)

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