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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 **8051 - 8075** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
4248	beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase	MGAT3 Aliases: GNT-III	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 Pick's disease Reye syndrome brachydactyly type C brachydactyly breast cancer cancer cerebral degeneration chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma hepatitis B hepatocellular carcinoma inflammatory bowel disease liver cancer ovarian cancer ovarian carcinoma papillary renal cell carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
4247	alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	MGAT2 Aliases: GNT-II	Homo sapiens (human)	Laron syndrome achondroplasia antithrombin III deficiency autosomal recessive chronic granulomatous disease 3 cancer chronic granulomatous disease clubfoot congenital disorder of glycosylation type II congenital disorder of glycosylation type IIa congenital disorder of glycosylation congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia craniosynostosis diabetes mellitus diabetic ketoacidosis disease of metabolism epilepsy factor XII deficiency gestational diabetes gingival hypertrophy gingival overgrowth microcephaly neuroblastoma obesity protein C deficiency protein S deficiency sensorineural hearing loss stereotypic movement disorder syndromic X-linked intellectual disability 94 thrombophilia type 2 diabetes mellitus ventricular septal defect visual epilepsy
4246	secretoglobin family 2A member 1	SCGB2A1	Homo sapiens (human)
4245	alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	MGAT1 Aliases: GLCNAC-TI GNT-1 GnTI	Homo sapiens (human)	Balo concentric sclerosis adrenoleukodystrophy breast cancer breast carcinoma cancer cardiomyopathy cardiovascular system disease central nervous system cancer central nervous system disease complex partial epilepsy congestive heart failure cystinuria diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy disease of mental health disease of metabolism embryoma endomyocardial fibrosis epilepsy galactokinase deficiency galactosemia gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycine encephalopathy glycogen storage disease Ia glycogen storage disease heart disease hepatocellular carcinoma high grade glioma hypertrophic cardiomyopathy inflammatory bowel disease liver cancer mixed glioma multiple sclerosis narcolepsy nervous system disease obesity obsolete type 1 diabetes mellitus 9 prostate cancer prostate carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder temporal lobe epilepsy 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 visual epilepsy
4242	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	MFNG	Homo sapiens (human)
4241	melanotransferrin	MELTF Aliases: CD228 FLJ38863 MAP97 MGC4856 MTF1 MTf melanotransferrin membrane-bound transferrin-like protein	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 MHC class II deficiency Pick's disease Reye syndrome Roberts syndrome Zollinger-Ellison syndrome adenosine deaminase deficiency angiomyolipoma astigmatism bone osteosarcoma cancer carcinoma central nervous system cancer cerebral degeneration cerebral primitive neuroectodermal tumor cervical cancer cervix carcinoma childhood osteosarcoma colorectal cancer colorectal carcinoma dysplastic nevus syndrome embryoma gliosarcoma high grade glioma hyperinsulinism large intestine cancer lung adenocarcinoma lung cancer medulloblastoma medulloepithelioma melanoma melanotic neuroectodermal tumor mixed glioma neuroectodermal tumor obsolete SC phocomelia syndrome obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered osteosarcoma polycystic ovary syndrome sarcomatoid carcinoma severe combined immunodeficiency skin melanoma stomach cancer stomach carcinoma supratentorial primitive neuroectodermal tumor
4240	milk fat globule EGF and factor V/VIII domain containing	MFGE8	Homo sapiens (human)
4239	microfibril associated protein 4	MFAP4	Homo sapiens (human)
4238	microfibril associated protein 3	MFAP3	Homo sapiens (human)
4237	microfibril associated protein 2	MFAP2	Homo sapiens (human)
4236	microfibril associated protein 1	MFAP1	Homo sapiens (human)
4233	MET proto-oncogene, receptor tyrosine kinase	MET	Homo sapiens (human)
4232	mesoderm specific transcript	MEST Aliases: PEG1 Paternally-expressed gene 1	Homo sapiens (human)
4225	meprin A subunit beta	MEP1B	Homo sapiens (human)
4224	meprin A subunit alpha	MEP1A	Homo sapiens (human)
4216	mitogen-activated protein kinase kinase kinase 4	MAP3K4	Homo sapiens (human)
4214	mitogen-activated protein kinase kinase kinase 1	MAP3K1	Homo sapiens (human)
4211	Meis homeobox 1	MEIS1	Homo sapiens (human)
4210	MEFV innate immunity regulator, pyrin	MEFV	Homo sapiens (human)
4209	myocyte enhancer factor 2D	MEF2D	Homo sapiens (human)
4208	myocyte enhancer factor 2C	MEF2C	Homo sapiens (human)
4207	BORCS8-MEF2B readthrough	BORCS8-MEF2B	Homo sapiens (human)
4205	myocyte enhancer factor 2A	MEF2A	Homo sapiens (human)
4204	methyl-CpG binding protein 2	MECP2	Homo sapiens (human)
4200	malic enzyme 2	ME2 Aliases: NAD-dependent malic enzyme, mitochondrial malate dehydrogenase (oxaloacetate-decarboxylating)	Homo sapiens (human)	bipolar disorder cancer embryoma epilepsy generalized epilepsy with febrile seizures plus giant cell glioblastoma glioblastoma high grade glioma idiopathic generalized epilepsy leukemia lung benign neoplasm lung cancer lung non-small cell carcinoma microphthalmia obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder

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