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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 **7876 - 7900** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
51246	shisa family member 5	SHISA5	Homo sapiens (human)
388336	shisa family member 6	SHISA6	Homo sapiens (human)
729956	shisa family member 7	SHISA7	Homo sapiens (human)
440829	shisa family member 8	SHISA8	Homo sapiens (human)
729993	shisa family member 9	SHISA9	Homo sapiens (human)
85352	shisa like 1	SHISAL1	Homo sapiens (human)
100132916	shisa like 2B	SHISAL2B	Homo sapiens (human)
6470	serine hydroxymethyltransferase 1	SHMT1 Aliases: 14 kDa protein MGC15229 MGC24556 SHMT cSHMT cytoplasmic serine hydroxymethyltransferase	Homo sapiens (human)	B-cell lymphoma Burkitt lymphoma Down syndrome Langerhans-cell histiocytosis Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease acute lymphoblastic leukemia acute myeloid leukemia adenocarcinoma adenoma adenosarcoma adult acute lymphocytic leukemia alcohol use disorder alopecia alternating hemiplegia of childhood autistic disorder autonomic neuropathy bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease central nervous system disease central nervous system lymphoma cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia childhood leukemia chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital heart disease cribriform carcinoma embryoma epilepsy esophagus squamous cell carcinoma essential hypertension follicular adenoma gastric cardia adenocarcinoma granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hepatocellular carcinoma hyperhomocysteinemia hyperphosphatemia hypertension intestinal benign neoplasm intestinal cancer large intestine cancer laryngeal benign neoplasm laryngeal disease larynx cancer leukemia liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lymphoma microcystic adenoma multiple sclerosis nephroblastoma nervous system disease non-Hodgkin lymphoma obsolete ymphosarcoma optic papillitis ovarian cancer ovarian carcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma papilledema prostate cancer prostate carcinoma reticulosarcoma retinal edema sarcomatoid carcinoma schizophrenia situs inversus squamous cell carcinoma temporal arteritis thyroid gland medullary carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma tracheal disease tuberous sclerosis tubular adenocarcinoma urinary bladder cancer
6472	serine hydroxymethyltransferase 2	SHMT2 Aliases: mSHMT mitochondrial serine hydroxymethyltransferase	Homo sapiens (human)	B-cell lymphoma Down syndrome Langerhans-cell histiocytosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease alcohol use disorder anemia arthritis arthropathy autistic disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cholangiocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma gastrointestinal system cancer gliosarcoma head and neck squamous cell carcinoma hepatitis B hepatocellular carcinoma high grade glioma idiopathic interstitial pneumonia idiopathic pulmonary fibrosis intrahepatic cholangiocarcinoma large intestine cancer liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma macrocytic anemia mixed glioma neuroblastoma non-Hodgkin lymphoma obsolete ymphosarcoma osteoarthritis prostate cancer prostate carcinoma reticulosarcoma schizophrenia stomach cancer stomach carcinoma
8036	SHOC2 leucine rich repeat scaffold protein	SHOC2	Homo sapiens (human)
23729	sedoheptulokinase	SHPK	Homo sapiens (human)
57619	shroom family member 3	SHROOM3	Homo sapiens (human)
57477	shroom family member 4	SHROOM4	Homo sapiens (human)
57698	shootin 1	SHTN1	Homo sapiens (human)
6476	sucrase-isomaltase	SI Aliases: Alpha-methylglucosidase Oligo-1,6-glucosidase Oligosaccharide alpha-1,6-glucosidase alpha-glucosidase	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 Barrett's esophagus Clostridium difficile colitis Duchenne muscular dystrophy Fabry disease Gaucher's disease Gerstmann-Straussler-Scheinker syndrome Gorham's disease Japanese encephalitis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome adenocarcinoma adenoma amyotrophic lateral sclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy brachydactyly type C brachydactyly cancer cardiomyopathy cardiovascular system disease cerebral degeneration chronic lymphocytic leukemia chylomicron retention disease colitis colorectal cancer colorectal carcinoma congenital disorder of glycosylation congenital muscular dystrophy congenital sucrase-isomaltase deficiency coronary artery disease cribriform carcinoma cystic fibrosis cystinuria dengue disease depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism distal myopathy embryoma endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hypertrophic cardiomyopathy familial periodic paralysis galactosemia gastric cardia adenocarcinoma gastroenteritis gastrointestinal system disease glucose intolerance glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease granular cell carcinoma heart disease hyperglycemia hypertrophic cardiomyopathy hypoglycemia ileitis ileocolitis intestinal disease irritable bowel syndrome kwashiorkor lactose intolerance large intestine cancer limb-girdle muscular dystrophy lipid storage disease lysosomal storage disease major depressive disorder marasmus melancholic depression muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myotonic dystrophy type 1 myotonic dystrophy type 2 nephrolithiasis neurocirculatory asthenia neurodegenerative disease nutmeg liver nutrition disease obesity obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete melancholia oculopharyngeal muscular dystrophy peptic ulcer disease prediabetes syndrome progressive muscular atrophy prolactinoma protein-energy malnutrition punctate palmoplantar keratoderma type III rippling muscle disease 2 sudden infant death syndrome tropical sprue tubular adenocarcinoma type 2 diabetes mellitus uric acid nephrolithiasis viral infectious disease yellow fever
54414	sialic acid acetylesterase	SIAE	Homo sapiens (human)	autoimmune disease
6477	siah E3 ubiquitin protein ligase 1	SIAH1	Homo sapiens (human)
54847	SID1 transmembrane family member 1	SIDT1	Homo sapiens (human)
51092	SID1 transmembrane family member 2	SIDT2	Homo sapiens (human)
59307	single Ig and TIR domain containing	SIGIRR	Homo sapiens (human)
6614	sialic acid binding Ig like lectin 1	SIGLEC1 Aliases: CD169 FLJ00051 FLJ00055 FLJ00073 FLJ32150 SIGLEC-1 dJ1009E24.1 sialoadhesin	Homo sapiens (human)	Ebola hemorrhagic fever Graves' disease Kaposi's sarcoma Marfan syndrome St. Louis encephalitis allergic asthma anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ascariasis ascaridiasis asthma atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome bladder carcinoma breast cancer breast carcinoma cancer childhood leukemia chronic fatigue syndrome colitis common cold congenital heart block coronary artery disease diabetes mellitus embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma esophageal cancer esophageal carcinoma gastroenteritis glomerulonephritis head and neck squamous cell carcinoma hepatitis B hepatitis C hyperthyroidism ileitis ileocolitis immune system disease influenza intrinsic asthma kidney disease leukemia liver cirrhosis lupus erythematosus macrocytic anemia melanoma multiple myeloma multiple sclerosis myelitis nephritis nephrosis nutmeg liver prostate cancer prostate carcinoma pulmonary tuberculosis pyoureter respiratory syncytial virus infectious disease rheumatoid arthritis scleroderma situs inversus skin melanoma steatotic liver disease systemic lupus erythematosus systemic scleroderma thyrotoxicosis tuberculosis tuberculous pneumothorax tuberous sclerosis type 2 diabetes mellitus urinary bladder cancer viral infectious disease
89790	sialic acid binding Ig like lectin 10	SIGLEC10 Aliases: MGC126774 PRO940 SIGLEC-10 SLG2 sialic acid binding Ig-like lectin 10 Ig-like lectin 7 siglec-like gene 2	Homo sapiens (human)	B-cell lymphoma cancer childhood leukemia leukemia obsolete ymphosarcoma
114132	sialic acid binding Ig like lectin 11	SIGLEC11	Homo sapiens (human)
89858	sialic acid binding Ig like lectin 12	SIGLEC12 Aliases: S2V SLG Siglec-12 Siglec-L1 Siglec-XII	Homo sapiens (human)	carcinoma chronic fatigue syndrome disease of metabolism encephalomyelitis obesity prostate cancer prostate carcinoma sarcomatoid carcinoma systemic lupus erythematosus
100049587	sialic acid binding Ig like lectin 14	SIGLEC14	Homo sapiens (human)

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