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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 **7226 - 7250** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
6328	sodium voltage-gated channel alpha subunit 3	SCN3A	Homo sapiens (human)
6327	sodium voltage-gated channel beta subunit 2	SCN2B	Homo sapiens (human)
6326	sodium voltage-gated channel alpha subunit 2	SCN2A	Homo sapiens (human)
6324	sodium voltage-gated channel beta subunit 1	SCN1B	Homo sapiens (human)
6323	sodium voltage-gated channel alpha subunit 1	SCN1A	Homo sapiens (human)
6320	C-type lectin domain containing 11A	CLEC11A	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
6317	serpin family B member 3	SERPINB3	Homo sapiens (human)
6314	ataxin 7	ATXN7	Homo sapiens (human)
6311	ataxin 2	ATXN2	Homo sapiens (human)
6310	ataxin 1	ATXN1	Homo sapiens (human)
6309	sterol-C5-desaturase	SC5D Aliases: delta(7)-sterol 5(6)-desaturase lathosterol oxidase	Homo sapiens (human)	Marfan syndrome Peters anomaly Smith-Lemli-Opitz syndrome Unverricht-Lundborg syndrome basal cell carcinoma blepharospasm cataract cleft palate clubfoot complex partial epilepsy congenital heart disease congenital ptosis cornea plana early myoclonic encephalopathy epilepsy focal hand dystonia gallbladder disease gingival hypertrophy gingival overgrowth intellectual disability intrahepatic cholestasis isolated cleft palate learning disability liver disease meningocele microcephaly placental insufficiency polydactyly ptosis sensorineural hearing loss situs inversus temporal lobe epilepsy thrombocytopenia tuberous sclerosis visual epilepsy
6307	methylsterol monooxygenase 1	MSMO1 Aliases: DESP4 ERG25	Homo sapiens (human)	Laron syndrome achondroplasia actinic keratosis blepharitis cancer chondrodysplasia punctata diabetes mellitus embryoma ichthyosis idiopathic scoliosis microcephaly obesity parapsoriasis psoriasis pustulosis of palm and sole seborrheic keratosis skin disease type 2 diabetes mellitus
6304	SATB homeobox 1	SATB1	Homo sapiens (human)
6302	tetraspanin 31	TSPAN31	Homo sapiens (human)
6301	seryl-tRNA synthetase 1	SARS1	Homo sapiens (human)
6299	spalt like transcription factor 1	SALL1	Homo sapiens (human)
6297	spalt like transcription factor 2	SALL2	Homo sapiens (human)
6296	acyl-CoA synthetase medium chain family member 3	ACSM3 Aliases: SA	Homo sapiens (human)	IgA glomerulonephritis Kallmann syndrome Marfan syndrome Sheehan syndrome abdominal obesity-metabolic syndrome 1 anemia autism spectrum disorder autistic disorder bacterial sepsis brain cancer brain stem infarction breast cancer breast carcinoma cancer cardiovascular system disease cataract cerebral artery occlusion cerebral infarction cerebrovascular disease chronic kidney disease communicating hydrocephalus diabetes mellitus diabetic ketoacidosis embryoma epilepsy essential hypertension essential thrombocythemia generalized atherosclerosis heart disease hemosiderosis hepatocellular carcinoma hereditary coproporphyria hydrocephalus hyperglycemia hypertension hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism idiopathic scoliosis intracranial aneurysm intracranial vasospasm isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency liver cancer liver carcinoma macrocytic anemia obesity obstructive hydrocephalus ocular hypertension oculomotor nerve paralysis panhypopituitarism partial third-nerve palsy post-traumatic stress disorder prostate cancer prostate carcinoma senile degeneration of brain sensorineural hearing loss situs inversus tetralogy of Fallot thrombophilia thymus gland disease total third-nerve palsy transient cerebral ischemia tuberous sclerosis ulcerative colitis visual epilepsy
6294	scaffold attachment factor B	SAFB	Homo sapiens (human)
6291	serum amyloid A4, constitutive	SAA4	Homo sapiens (human)
6272	sortilin 1	SORT1	Homo sapiens (human)
6263	ryanodine receptor 3	RYR3	Homo sapiens (human)
6262	ryanodine receptor 2	RYR2	Homo sapiens (human)
6261	ryanodine receptor 1	RYR1	Homo sapiens (human)

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