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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 **7501 - 7525** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
80824	dual specificity phosphatase 16	DUSP16	Homo sapiens (human)
80833	apolipoprotein L3	APOL3	Homo sapiens (human)
80834	taste 1 receptor member 2	TAS1R2	Homo sapiens (human)
80835	taste 1 receptor member 1	TAS1R1	Homo sapiens (human)
80852	glutamate receptor interacting protein 2	GRIP2	Homo sapiens (human)
80854	SET domain containing 7, histone lysine methyltransferase	SETD7	Homo sapiens (human)
80856	lunapark, ER junction formation factor	LNPK	Homo sapiens (human)
80864	EGF like domain multiple 8	EGFL8	Homo sapiens (human)
80896	N-acetylneuraminate pyruvate lyase	NPL Aliases: DHDPS1 NPL1 dihydrodipicolinate synthetase homolog 1 (E. coli)	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 Ewing sarcoma Pick's disease Reye syndrome alcohol dependence alcohol use disorder atopic dermatitis bipolar disorder cerebral degeneration cholestasis congestive heart failure dermatitis epilepsy essential hypertension generalized epilepsy with febrile seizures plus hypertension idiopathic generalized epilepsy inflammatory bowel disease 1 inflammatory bowel disease influenza juvenile myoclonic epilepsy myopathy obsolete major affective disorder 1 obsolete major affective disorder 2 panic disorder prostate cancer prostate carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder sensorineural hearing loss ulcerative colitis visual epilepsy
80975	transmembrane serine protease 5	TMPRSS5	Homo sapiens (human)
81027	tubulin beta 1 class VI	TUBB1	Homo sapiens (human)
81029	Wnt family member 5B	WNT5B	Homo sapiens (human)
81031	solute carrier family 2 member 10	SLC2A10 Aliases: GLUT-10 GLUT10 facilitative glucose transporter GLUT10	Homo sapiens (human)	Hailey-Hailey disease Legg-Calve-Perthes disease Loeys-Dietz syndrome Moyamoya disease Rothmund-Thomson syndrome X-linked dilated cardiomyopathy acute myocardial infarction adenocarcinoma adenoma adult respiratory distress syndrome allergic asthma aortic aneurysm aortic valve disease 2 aortic valve insufficiency aortic valve stenosis arterial tortuosity syndrome asthma autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB blepharophimosis bone disease breast cancer breast carcinoma bronchiolo-alveolar adenocarcinoma bronchus cancer bronchus carcinoma cancer cardiac arrest cardiomyopathy cartilage disease cataract 32 multiple types cerebral infarction cerebrovascular disease childhood type dermatomyositis chondrosarcoma collagen disease congenital central hypoventilation syndrome congenital diaphragmatic hernia congestive heart failure connective tissue disease corneal disease coronary thrombosis craniosynostosis cribriform carcinoma cutis laxa dermatomyositis diabetes mellitus diabetic ketoacidosis 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 endomyocardial fibrosis esophagitis essential hypertension familial hypertrophic cardiomyopathy gastroesophageal reflux disease granular cell carcinoma hiatus hernia hypertension hypertrophic cardiomyopathy hypertropia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis inguinal hernia intellectual disability intermittent claudication interstitial lung disease intrinsic asthma keratoconus learning disability leukocyte adhesion deficiency 1 leukocyte adhesion deficiency lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma mal de Meleda mechanical strabismus megalocornea myocardial infarction myocarditis myopia newborn respiratory distress syndrome obstructive lung disease omphalocele ophthalmoplegia peptic esophagitis peripheral artery disease peripheral vascular disease pneumonia pulmonary emphysema pyloric stenosis respiratory failure restrictive dermopathy scoliosis silent myocardial infarction strabismus thoracic aortic aneurysm tubular adenocarcinoma type 2 diabetes mellitus umbilical hernia vascular disease
81033	potassium voltage-gated channel subfamily H member 6	KCNH6	Homo sapiens (human)
81035	collectin subfamily member 12	COLEC12 Aliases: CL-P1 SCARA4 SRCL	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis diabetes mellitus familial periodic paralysis multiple sclerosis myopathy substance abuse substance-related disorder type 2 diabetes mellitus
81037	CLPTM1 like	CLPTM1L	Homo sapiens (human)
81050	olfactory receptor family 5 subfamily AC member 2	OR5AC2	Homo sapiens (human)
81061	olfactory receptor family 11 subfamily H member 1	OR11H1	Homo sapiens (human)
81127	olfactory receptor family 4 subfamily K member 15	OR4K15	Homo sapiens (human)
81168	olfactory receptor family 8 subfamily J member 3	OR8J3	Homo sapiens (human)
81282	olfactory receptor family 51 subfamily G member 2	OR51G2	Homo sapiens (human)
81285	olfactory receptor family 51 subfamily E member 2	OR51E2	Homo sapiens (human)
81300	olfactory receptor family 4 subfamily P member 4	OR4P4	Homo sapiens (human)
81309	olfactory receptor family 4 subfamily C member 15	OR4C15	Homo sapiens (human)
81318	olfactory receptor family 4 subfamily A member 5	OR4A5	Homo sapiens (human)

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