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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 **8876 - 8900** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
23450	splicing factor 3b subunit 3	SF3B3	Homo sapiens (human)
10262	splicing factor 3b subunit 4	SF3B4	Homo sapiens (human)
6433	splicing factor SWAP	SFSWAP	Homo sapiens (human)
6421	splicing factor proline and glutamine rich	SFPQ	Homo sapiens (human)
10418	spondin 1	SPON1	Homo sapiens (human)
10417	spondin 2	SPON2	Homo sapiens (human)
10253	sprouty RTK signaling antagonist 2	SPRY2	Homo sapiens (human)
161742	sprouty related EVH1 domain containing 1	SPRED1	Homo sapiens (human)
6713	squalene epoxidase	SQLE Aliases: squalene monooxygenase	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 breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cerebral degeneration colorectal cancer colorectal carcinoma embryoma esophagus squamous cell carcinoma hepatocellular carcinoma large intestine cancer liver cancer long QT syndrome lung benign neoplasm lung cancer lung carcinoma lung squamous cell carcinoma microphthalmia neuroendocrine carcinoma neuroendocrine tumor obsolete Matthew-Wood syndrome prostate cancer prostate carcinoma sick sinus syndrome steatotic liver disease tinea corporis
10505	ssemaphorin 4F	SEMA4F	Homo sapiens (human)
23166	stabilin 1	STAB1	Homo sapiens (human)
55576	stabilin 2	STAB2	Homo sapiens (human)
283726	stabilizer of axonemal microtubules 2	SAXO2	Homo sapiens (human)
6781	stanniocalcin 1	STC1	Homo sapiens (human)
8614	stanniocalcin 2	STC2	Homo sapiens (human)
27044	staphylococcal nuclease and tudor domain containing 1	SND1	Homo sapiens (human)
8987	starch binding domain 1	STBD1 Aliases: FLJ41801 GENX-3414 genethonin 1	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease glycogen storage disease II
3925	stathmin 1	STMN1	Homo sapiens (human)
6780	staufen double-stranded RNA binding protein 1	STAU1	Homo sapiens (human)
27067	staufen double-stranded RNA binding protein 2	STAU2	Homo sapiens (human)
6319	stearoyl-CoA desaturase	SCD Aliases: FADS5 SCD1 acyl-CoA desaturase delta-9-desaturase fatty acid desaturase	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 Bannayan-Riley-Ruvalcaba syndrome Bietti crystalline corneoretinal dystrophy Bloom syndrome Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome Cowden syndrome Fabry disease Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Japanese encephalitis Marfan syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Timothy syndrome Wolman disease Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 actinic keratosis acute lymphoblastic leukemia adenocarcinoma adenoma allergic asthma amyloidosis amyotrophic lateral sclerosis anemia anorexia nervosa antithrombin III deficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome basal cell carcinoma beta thalassemia bipolar disorder bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest cardiomyopathy cardiovascular system disease catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma chylomicron retention disease clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital hemolytic anemia congestive heart failure coronary artery disease cribriform carcinoma dementia dengue disease depressive disorder diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysthymic disorder embryoma endocrine exophthalmos endometrial cancer endometrial carcinoma endomyocardial fibrosis epidermodysplasia verruciformis essential hypertension eye disease familial combined hyperlipidemia familial hypertrophic cardiomyopathy gestational diabetes gliosarcoma glomerulonephritis glucose intolerance granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hemoglobin C disease hemoglobin D disease hemoglobin E disease hemoglobinopathy hepatitis C hepatocellular carcinoma high grade glioma homocystinuria hyperglycemia hyperinsulinism hypertension hyperthyroidism hypertrophic cardiomyopathy immune system disease intrinsic asthma kidney disease large intestine cancer lipid storage disease lipoatrophic diabetes mellitus lipodystrophy liver cancer liver carcinoma liver cirrhosis long QT syndrome 1 long QT syndrome 2 long QT syndrome lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma macrocytic anemia major depressive disorder mastitis melancholic depression melanoma metabolic dysfunction-associated steatohepatitis metabolic dysfunction-associated steatotic liver disease mitral valve insufficiency mitral valve prolapse mixed glioma morbid obesity myeloproliferative disorder with eosinophilia nephritis nephrosis neurotic disorder nonpapillary renal cell carcinoma nutmeg liver obesity obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive sleep apnea osteomalacia ovarian cancer ovarian carcinoma papillary adenocarcinoma papillary renal cell carcinoma patulous eustachian tube polycystic ovary syndrome postural orthostatic tachycardia syndrome prediabetes syndrome progressive muscular atrophy prostate adenocarcinoma prostate cancer prostate carcinoma protein C deficiency protein S deficiency pyoureter renal carcinoma renal cell carcinoma restrictive cardiomyopathy rheumatoid arthritis rickets sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia sebaceous carcinoma seborrheic keratosis sensorineural hearing loss sick sinus syndrome sickle cell anemia situs inversus skin disease skin melanoma splenic sequestration steatotic liver disease sweat gland cancer synovitis systemic primary carnitine deficiency disease thalassemia thrombophilia thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland papillary carcinoma thyrotoxicosis tuberous sclerosis 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 urinary bladder cancer uterine corpus cancer viral infectious disease yellow fever
79966	stearoyl-CoA desaturase 5	SCD5 Aliases: ACOD4 FADS4 FLJ21032 HSCD5	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 T-cell acute lymphoblastic leukemia acquired immunodeficiency syndrome age related macular degeneration ankylosing spondylitis arthritis arthropathy autosomal dominant nonsyndromic deafness 79 breast cancer cancer cardiomyopathy cerebral degeneration degeneration of macula and posterior pole depressive disorder diabetes mellitus embryoma endomyocardial fibrosis familial hypertrophic cardiomyopathy hepatocellular carcinoma human immunodeficiency virus infectious disease hypertrophic cardiomyopathy liver cancer macular degeneration melanoma osteoarthritis primary ciliary dyskinesia 1 primary ciliary dyskinesia primary immunodeficiency disease restrictive cardiomyopathy rheumatoid arthritis sickle cell anemia skin melanoma systemic lupus erythematosus systemic primary carnitine deficiency disease type 2 diabetes mellitus
161497	stereocilin	STRC	Homo sapiens (human)
23098	sterile alpha and TIR motif containing 1	SARM1 Aliases: KIAA0524 SAMD2 SARM	Homo sapiens (human)	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease alternating hemiplegia of childhood amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis type 6 amyotrophic lateral sclerosis anterior horn cell disease autonomic neuropathy autosomal recessive distal hereditary motor neuronopathy 1 bacterial sepsis central nervous system disease chronic obstructive pulmonary disease disease of metabolism frontotemporal dementia late onset Parkinson's disease lateral sclerosis motor neuron disease nervous system disease neurodegenerative disease neuropathy peripheral nervous system disease polyneuropathy progressive muscular atrophy prostate cancer prostate carcinoma steatotic liver disease stomach cancer stomach carcinoma substance abuse substance-related disorder
90378	sterile alpha motif domain containing 1	SAMD1	Homo sapiens (human)

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