GlyCosmos Portal

Table Filtering

Gene ID

Gene Name

Gene Symbol

Organism

Taxonomy ID

Disease Ontology

Disease Ontology ID

Gene Ontology

Gene Ontology ID

Display
results per page.

Clear

Submissions

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 **6301 - 6325** of **9988** in total

« First

‹ Prev

…

249

250

251

252

253

254

255

256

257

…

Next ›

Last »
Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
89853	multivesicular body subunit 12B	MVB12B	Homo sapiens (human)
4440	musashi RNA binding protein 1	MSI1	Homo sapiens (human)
124540	musashi RNA binding protein 2	MSI2	Homo sapiens (human)
4593	muscle associated receptor tyrosine kinase	MUSK	Homo sapiens (human)
4154	muscleblind like splicing regulator 1	MBNL1	Homo sapiens (human)
10150	muscleblind like splicing regulator 2	MBNL2	Homo sapiens (human)
90523	muscular LMNA interacting protein	MLIP	Homo sapiens (human)
4292	mutL homolog 1	MLH1	Homo sapiens (human)
4436	mutS homolog 2	MSH2	Homo sapiens (human)
4438	mutS homolog 4	MSH4	Homo sapiens (human)
2956	mutS homolog 6	MSH6	Homo sapiens (human)
4595	mutY DNA glycosylase	MUTYH Aliases: MYH	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Cowden 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 Lynch syndrome Muir-Torre syndrome Peutz-Jeghers syndrome acoustic neuroma adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma age related macular degeneration anal carcinoma in situ angiomatous meningioma arthritis arthropathy benign meningioma bile duct adenocarcinoma bile duct carcinoma bladder carcinoma bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cerebral convexity meningioma cervical squamous cell carcinoma cervix uteri carcinoma in situ childhood acute lymphocytic leukemia cholangiocarcinoma chromosome 10q23 deletion syndrome clear cell meningioma colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart cribriform carcinoma deafness-dystonia-optic neuronopathy syndrome degeneration of macula and posterior pole depressive disorder diabetes mellitus diabetic ketoacidosis distal arthrogryposis dysthymic disorder embryoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis 2 familial adenomatous polyposis female breast carcinoma fibrous meningioma follicular adenoma gastroenteritis gastrointestinal system cancer gastrointestinal system disease gliosarcoma granular cell carcinoma hair follicle neoplasm head and neck cancer head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intestinal disease intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma islet cell tumor juvenile polyposis syndrome large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoplasmacyte-rich meningioma macular degeneration major depressive disorder melancholic depression melanoma meningioma meningothelial meningioma microcystic adenoma microcystic meningioma mixed glioma myeloproliferative neoplasm nervous system cancer neurodegenerative disease neuroendocrine carcinoma neuroendocrine tumor neurotic disorder obsolete melancholia olfactory groove meningioma osteoarthritis ovarian cancer pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenoma parasagittal meningioma pilomatrixoma pituitary adenoma primary open angle glaucoma proctitis prostate cancer prostate carcinoma psammomatous meningioma rectal benign neoplasm rectum adenocarcinoma rectum cancer rheumatoid arthritis sarcomatoid carcinoma sebaceous adenocarcinoma secretory meningioma skin melanoma spinal meningioma stomach cancer stomach carcinoma in situ stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma transitional meningioma transthyretin amyloidosis trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis urinary bladder cancer uterine corpus cancer von Hippel-Lindau disease
4099	myelin associated glycoprotein	MAG	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 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 type 5 Charcot-Marie-Tooth disease Guillain-Barre syndrome Kearns-Sayre syndrome Lewy body dementia MASA syndrome Marfan syndrome Mast syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pelizaeus-Merzbacher disease Pick's disease Reye syndrome SPOAN syndrome Troyer syndrome acute myocardial infarction adrenoleukodystrophy agenesis of the corpus callosum with peripheral neuropathy alternating hemiplegia of childhood amyloidosis angioma serpiginosum arteriosclerotic cardiovascular disease astigmatism atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy brain stem infarction cancer capillary hemangioma cavernous hemangioma central nervous system cancer central nervous system disease cerebellar ataxia cerebellar disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease chorioangioma chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy compartment syndrome congenital diarrhea 5 with tufting enteropathy congenital nystagmus coronary artery disease coronary thrombosis critical illness polyneuropathy demyelinating disease demyelinating polyneuropathy depressive disorder disease of mental health dissociated nystagmus dysthymic disorder embryoma familial multiple nevi flammei gliosarcoma glomus tumor hemangioma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia high grade glioma histiocytoid hemangioma hyperopia immune system disease inflammatory and toxic neuropathy intellectual disability intramuscular hemangioma learning disability lesion of sciatic nerve leukodystrophy lymphangioma major depressive disorder melancholic depression melanoma meningoencephalitis middle cerebral artery infarction mixed glioma monoclonal gammopathy of uncertain significance monoclonal paraproteinemia motor peripheral neuropathy multiple sclerosis myocardial infarction nerve compression syndrome nervous system disease neuroblastoma neuromuscular disease neuropathy neurotic disorder obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia optic atrophy optic neuritis pancreatic cancer paraplegia pathologic nystagmus peripheral nervous system disease placental insufficiency plasma cell neoplasm poikiloderma with neutropenia polyneuropathy polyradiculoneuropathy prostate cancer prostate carcinoma psychotic disorder schizophrenia sciatic neuropathy secondary Parkinson disease silent myocardial infarction situs inversus skin melanoma spontaneous ocular nystagmus substance abuse substance-related disorder trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis
4155	myelin basic protein	MBP	Homo sapiens (human)
4340	myelin oligodendrocyte glycoprotein	MOG	Homo sapiens (human)
4359	myelin protein zero	MPZ	Homo sapiens (human)
9019	myelin protein zero like 1	MPZL1	Homo sapiens (human)
10205	myelin protein zero like 2	MPZL2	Homo sapiens (human)
196264	myelin protein zero like 3	MPZL3	Homo sapiens (human)
745	myelin regulatory factor	MYRF	Homo sapiens (human)
196446	myelin regulatory factor like	MYRFL	Homo sapiens (human)
4332	myeloid cell nuclear differentiation antigen	MNDA	Homo sapiens (human)
7593	myeloid zinc finger 1	MZF1	Homo sapiens (human)
26579	myeloma overexpressed	MYEOV	Homo sapiens (human)
4353	myeloperoxidase	MPO	Homo sapiens (human)