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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 **8151 - 8175** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
4052	latent transforming growth factor beta binding protein 1	LTBP1	Homo sapiens (human)
4051	cytochrome P450 family 4 subfamily F member 3	CYP4F3 Aliases: CYP4F	Homo sapiens (human)	Bartter 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 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 3 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 Clostridium difficile colitis Conn's syndrome Crohn's colitis Crohn's disease Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Plasmodium vivax malaria Waterhouse-Friderichsen syndrome acoustic neuroma acquired immunodeficiency syndrome acute intermittent porphyria acute lymphoblastic leukemia acute myocardial infarction adrenal adenoma adrenal cortex cancer adrenal gland cancer adrenal gland hyperfunction adult acute lymphocytic leukemia agenesis of the corpus callosum with peripheral neuropathy alcohol use disorder allergic asthma anaplastic astrocytoma angiomatous meningioma asthma attention deficit hyperactivity disorder bacterial sepsis benign meningioma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease cerebral convexity meningioma cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia childhood cerebral astrocytoma choriocarcinoma clear cell meningioma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital adrenal hyperplasia congenital aphakia congestive heart failure coronary thrombosis cystinuria diabetes mellitus embryoma endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis epilepsy essential hypertension fibrillary astrocytoma fibrous meningioma galactosemia gallbladder disease gastric cardia carcinoma gemistocytic astrocytoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease gout heart disease hepatitis C hepatoblastoma hepatocellular carcinoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 1A hereditary sensory neuropathy hidradenitis suppurativa hidradenitis high grade glioma human immunodeficiency virus infectious disease hypertension inflammatory bowel disease 1 inflammatory bowel disease intraorbital meningioma intraventricular meningioma intrinsic asthma irritable bowel syndrome juvenile pilocytic astrocytoma kidney cancer kidney failure large intestine cancer laryngeal squamous cell carcinoma leiomyoma lingual-facial-buccal dyskinesia liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoplasmacyte-rich meningioma malignant astrocytoma meningioma meningothelial meningioma microcystic meningioma motor peripheral neuropathy myocardial infarction myofibroma neurocirculatory asthenia obesity obsolete Cushing's syndrome obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum olfactory groove meningioma pancreatic ductal adenocarcinoma parasagittal meningioma patent ductus arteriosus pilocytic astrocytoma pituitary adenoma placenta cancer pompholyx primary hyperaldosteronism prostate cancer prostate carcinoma protoplasmic astrocytoma psammomatous meningioma sarcomatoid carcinoma schizophrenia secretory meningioma sensory peripheral neuropathy silent myocardial infarction spinal meningioma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma sudden infant death syndrome tongue squamous cell carcinoma transitional meningioma tuberculosis type 2 diabetes mellitus ulcerative colitis uterine corpus cancer uterine fibroid viral infectious disease visual epilepsy
4050	lymphotoxin beta	LTB	Homo sapiens (human)
4049	lymphotoxin alpha	LTA	Homo sapiens (human)
4048	leukotriene A4 hydrolase	LTA4H	Homo sapiens (human)	Burkitt lymphoma Buruli ulcer disease Crohn's colitis Crohn's disease Down syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute myocardial infarction adenocarcinoma adenoma allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis bacterial meningitis cancer cardiovascular system disease cerebral infarction cerebrovascular disease chronic myeloid leukemia colorectal cancer colorectal carcinoma coronary artery disease coronary thrombosis cribriform carcinoma depressive disorder dysthymic disorder embryoma familial nephrotic syndrome granular cell carcinoma heart disease human immunodeficiency virus infectious disease idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma large intestine cancer laryngeal squamous cell carcinoma leprosy lipoid nephrosis major depressive disorder melancholic depression melanoma myeloproliferative disorder with eosinophilia myocardial infarction nephrotic syndrome neurotic disorder obsolete melancholia pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma pulmonary tuberculosis silent myocardial infarction skin benign neoplasm skin cancer skin melanoma squamous cell carcinoma squamous cell neoplasm tongue squamous cell carcinoma tuberculosis tuberculous pneumothorax tubular adenocarcinoma ulcerative colitis viral meningitis
4047	lanosterol synthase	LSS Aliases: OSC Oxidosqualene-lanosterol cyclase	Homo sapiens (human)	Baraitser-Winter syndrome Fabry disease Fraser syndrome Goldenhar syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Q fever Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome Wolman disease acquired immunodeficiency syndrome acute lymphoblastic leukemia adult acute lymphocytic leukemia alopecia-mental retardation syndrome 4 alopecia ankylosing spondylitis arteriosclerotic cardiovascular disease atherosclerosis blindness bone osteosarcoma branchiootic syndrome breast cancer breast carcinoma cancer cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract central nervous system cancer childhood acute lymphocytic leukemia childhood osteosarcoma chylomicron retention disease coronary artery disease diffuse idiopathic skeletal hyperostosis embryoma endometrial serous adenocarcinoma epilepsy epithelioid sarcoma essential hypertension giant cell glioblastoma glioblastoma gliosarcoma high grade glioma holoprosencephaly 1 holoprosencephaly human immunodeficiency virus infectious disease hypertension hypotrichosis 14 hypotrichosis 1 hypotrichosis intellectual disability learning disability lipid storage disease microcephaly mixed glioma orofaciodigital syndrome I orofaciodigital syndrome X ossification of the posterior longitudinal ligament of spine osteosarcoma ovary serous adenocarcinoma primary sclerosing cholangitis sarcoma sclerosing cholangitis senile cataract skin disease spinal stenosis spindle cell sarcoma squamous cell carcinoma tongue cancer tongue squamous cell carcinoma trypanosomiasis typhus visual epilepsy
4046	lymphocyte specific protein 1	LSP1	Homo sapiens (human)
4045	limbic system associated membrane protein	LSAMP	Homo sapiens (human)
4043	LDL receptor related protein associated protein 1	LRPAP1	Homo sapiens (human)
4041	LDL receptor related protein 5	LRP5	Homo sapiens (human)	Worth syndrome autosomal dominant osteopetrosis 1 autosomal dominant polycystic kidney disease exudative vitreoretinopathy 4 exudative vitreoretinopathy heart valve disease idiopathic juvenile osteoporosis microphthalmia neovascular inflammatory vitreoretinopathy nonsyndromic deafness osteonecrosis osteoporosis-pseudoglioma syndrome osteoporosis polycystic liver disease tendinitis
4040	LDL receptor related protein 6	LRP6	Homo sapiens (human)
4038	LDL receptor related protein 4	LRP4	Homo sapiens (human)
4037	LDL receptor related protein 3	LRP3	Homo sapiens (human)
4036	LDL receptor related protein 2	LRP2	Homo sapiens (human)
4035	LDL receptor related protein 1	LRP1	Homo sapiens (human)
4034	leucine rich repeats and calponin homology domain containing 4	LRCH4	Homo sapiens (human)
4033	inositol 1,4,5-triphosphate receptor associated 2	IRAG2	Homo sapiens (human)
4026	LIM domain containing preferred translocation partner in lipoma	LPP	Homo sapiens (human)
4025	lactoperoxidase	LPO	Homo sapiens (human)
4023	lipoprotein lipase	LPL	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 Crohn's colitis Crohn's disease Fabry disease Fanconi anemia complementation group A Fanconi anemia Friedreich ataxia 1 Friedreich ataxia Gilbert 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 Norum disease Pick's disease Reye syndrome Richter's syndrome Tangier disease Wolman disease X-linked dilated cardiomyopathy Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 abetalipoproteinemia acne acromegaly acute chest syndrome acute lymphoblastic leukemia acute myocardial infarction acute pancreatitis adenocarcinoma adenoma age related macular degeneration alcoholic pancreatitis aortic atherosclerosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal recessive hypercholesterolemia bilirubin metabolic disorder bone osteosarcoma brain infarction brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease carotid artery thrombosis carotid stenosis celiac disease central nervous system cancer cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease childhood osteosarcoma cholesterol-ester transfer protein deficiency choreaacanthocytosis chronic kidney disease chronic lymphocytic leukemia chylomicron retention disease colon cancer colonic benign neoplasm colorectal cancer congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congestive heart failure coronary artery disease coronary stenosis coronary thrombosis cribriform carcinoma cystic lymphangioma cystinuria degeneration of macula and posterior pole dementia diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma 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 disease of metabolism eclampsia embryoma embryonal cancer end stage renal disease endometrial cancer endometrial carcinoma endomyocardial fibrosis epilepsy essential hypertension extramedullary plasmacytoma familial apolipoprotein A5 deficiency familial apolipoprotein C-II deficiency familial combined hyperlipidemia familial hypercholesterolemia familial hyperlipidemia familial lipase maturation factor 1 deficiency familial lipoprotein lipase deficiency familial partial lipodystrophy type 2 familial partial lipodystrophy focal segmental glomerulosclerosis follicular lymphoma galactosemia germ cell and embryonal cancer germ cell cancer germinoma gestational diabetes gliosarcoma glucose intolerance glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease granular cell carcinoma heart disease hematologic cancer hepatitis C hepatocellular carcinoma high grade glioma hyperalphalipoproteinemia 1 hyperglycemia hyperinsulinism hyperlipoproteinemia type III hyperlipoproteinemia type IV hyperlipoproteinemia type V hyperpituitarism hyperprolactinemia hypertension hypertrophic cardiomyopathy hypoglycemia hypolipoproteinemia impotence inflammatory bowel disease 1 inflammatory bowel disease isolated growth hormone deficiency large intestine cancer lipid storage disease lipoatrophic diabetes mellitus lipodystrophy liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lymphoblastic lymphoma lymphoplasmacytic lymphoma macroglobulinemia macular degeneration maple syrup urine disease mastitis metabolic dysfunction-associated steatotic liver disease mixed glioma monoclonal gammopathy of uncertain significance morbid obesity multiple myeloma multiple sclerosis muscular disease myocardial infarction myotonic dystrophy type 1 myotonic dystrophy type 2 neurodegenerative disease nodular prostate nutmeg liver obesity obsolete familial hypertriglyceridemia obsolete lymphoplasmacytic lymphoma obsolete type 1 diabetes mellitus 9 osteosarcoma ovarian hyperstimulation syndrome overnutrition pancreatitis peripheral artery disease placental insufficiency plasma cell neoplasm plasmacytoma polycystic ovary syndrome polycythemia vera pre-eclampsia prediabetes syndrome premature ejaculation prostate cancer prostate carcinoma prostatic adenoma psychologic dyspareunia sarcomatoid carcinoma schizophrenia silent myocardial infarction steatotic liver disease thrombophilia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tubular adenocarcinoma 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 type 2 diabetes mellitus ulcerative colitis uterine corpus cancer vascular disease visceral leishmaniasis
4018	lipoprotein(a)	LPA	Homo sapiens (human)
4017	lysyl oxidase like 2	LOXL2	Homo sapiens (human)
4016	lysyl oxidase like 1	LOXL1	Homo sapiens (human)
4015	lysyl oxidase	LOX	Homo sapiens (human)
4012	leucyl and cystinyl aminopeptidase	LNPEP	Homo sapiens (human)

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