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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 **8701 - 8725** of **9988** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
150572	SET and MYND domain containing 1	SMYD1	Homo sapiens (human)
150681	olfactory receptor family 6 subfamily B member 3	OR6B3	Homo sapiens (human)
150696	prominin 2	PROM2	Homo sapiens (human)
150709	ankyrin and armadillo repeat containing	ANKAR	Homo sapiens (human)
150763	glycerol-3-phosphate acyltransferase 2, mitochondrial	GPAT2 Aliases: CT123 cancer/testis antigen 123	Homo sapiens (human)	adrenoleukodystrophy breast cancer breast carcinoma cancer melanoma skin melanoma
150864	family with sequence similarity 117 member B	FAM117B	Homo sapiens (human)
150962	pseudouridine synthase 10	PUS10	Homo sapiens (human)
151056	phospholipase B1	PLB1 Aliases: FLJ30866 PLB	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 Balo concentric sclerosis Barrett's esophagus Crohn's colitis Crohn's disease Guillain-Barre syndrome IgA glomerulonephritis IgG4-related disease Krabbe disease Kufor-Rakeb syndrome Marfan syndrome Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Werner syndrome West Nile fever X-linked chronic granulomatous disease acoustic neuroma acute chest syndrome acute myeloid leukemia acute myocardial infarction adrenoleukodystrophy adult respiratory distress syndrome allergic asthma allergic rhinitis alternating hemiplegia of childhood anaplastic astrocytoma angiomatous meningioma anthrax disease arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma ataxia telangiectasia atherosclerosis atopic dermatitis autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy autosomal dominant cerebellar ataxia autosomal dominant distal hereditary motor neuronopathy 2 bacterial infectious disease bacterial sepsis basal ganglia disease benign meningioma benign mesothelioma bipolar disorder blepharospasm blood coagulation disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis cardiac arrest cardiovascular system disease cataract central nervous system disease cerebral convexity meningioma cerebral degeneration childhood cerebral astrocytoma chronic ethmoiditis chronic fatigue syndrome chronic granulomatous disease chronic interstitial cystitis chronic kidney disease chronic obstructive pulmonary disease chronic sphenoidal sinusitis clear cell meningioma clonorchiasis colitis colon adenocarcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma complement deficiency coronary artery disease coronary thrombosis cryptococcosis cryptosporidiosis cystic fibrosis depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy dysthymic disorder embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma esophagitis esophagus adenocarcinoma familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperlipidemia familial nephrotic syndrome fibrillary astrocytoma fibrous meningioma focal hand dystonia focal segmental glomerulosclerosis fragile X-associated tremor/ataxia syndrome gastroduodenal Crohn's disease gastroenteritis gastroesophageal reflux disease gemistocytic astrocytoma glaucoma glomerulonephritis glucose intolerance heart disease hepatitis C hepatocellular carcinoma hereditary spastic paraplegia 35 high grade glioma hyperglycemia ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease intermediate coronary syndrome interstitial cystitis intraorbital meningioma intraventricular meningioma intrinsic asthma islet cell tumor isovaleric acidemia jejunoileitis juvenile pilocytic astrocytoma keratitis keratoconjunctivitis kidney disease large intestine cancer leukemia leukodystrophy lingual-facial-buccal dyskinesia lipoid nephrosis liver cancer liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphangioleiomyomatosis lymphoplasmacyte-rich meningioma macular corneal dystrophy major depressive disorder malignant astrocytoma malignant mesothelioma mastitis melancholic depression membranous glomerulonephritis meningioma meningothelial meningioma microcystic meningioma mood disorder movement disease multiple sclerosis myelitis myocardial infarction narcolepsy nasopharynx carcinoma nephritis nephrosis nephrotic syndrome nervous system disease neuroaxonal dystrophy neuroblastoma neurodegeneration with brain iron accumulation 2a neurodegeneration with brain iron accumulation 2b neurodegeneration with brain iron accumulation 3 neurodegeneration with brain iron accumulation 4 neurodegeneration with brain iron accumulation 5 neurodegeneration with brain iron accumulation 6 neurodegeneration with brain iron accumulation neurodegenerative disease neurotic disorder newborn respiratory distress syndrome nutmeg liver obesity obsolete inherited blood coagulation disease obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia olfactory groove meningioma oral candidiasis osteoarthritis ovarian cancer ovarian carcinoma pantothenate kinase-associated neurodegeneration parapsoriasis parasagittal meningioma patent ductus arteriosus peptic esophagitis pilocytic astrocytoma pituitary adenoma pre-eclampsia prediabetes syndrome primary open angle glaucoma progeria prostate cancer prostate carcinoma protoplasmic astrocytoma psammomatous meningioma psoriasis pulmonary coin lesion pustulosis of palm and sole pyoureter rheumatoid arthritis sarcoidosis schizophrenia secondary Parkinson disease secretory meningioma sick sinus syndrome silent myocardial infarction situs inversus spinal meningioma spinocerebellar ataxia type 2 subependymal giant cell astrocytoma systemic lupus erythematosus thrombophilia transitional meningioma tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus ulcerative colitis uterine corpus cancer uveoparotid fever vascular disease vasculitis vasomotor rhinitis vulvovaginitis
151112	zinc finger SWIM-type containing 2	ZSWIM2	Homo sapiens (human)
151176	erythroferrone	ERFE	Homo sapiens (human)
151254	C2 calcium dependent domain containing 6	C2CD6	Homo sapiens (human)
151258	solute carrier family 38 member 11	SLC38A11	Homo sapiens (human)
151306	G protein-coupled bile acid receptor 1	GPBAR1	Homo sapiens (human)
151449	growth differentiation factor 7	GDF7	Homo sapiens (human)
151516	aspartic peptidase retroviral like 1	ASPRV1	Homo sapiens (human)
151531	uridine phosphorylase 2	UPP2 Aliases: UDRPASE2 UP2 UPASE2	Homo sapiens (human)	autism spectrum disorder autistic disorder cancer depressive disorder diabetes mellitus major depressive disorder melancholic depression obsolete melancholia squamous cell carcinoma tarsal-carpal coalition syndrome tongue squamous cell carcinoma transitional cell carcinoma type 2 diabetes mellitus
151556	G protein-coupled receptor 155	GPR155	Homo sapiens (human)
151613	tetratricopeptide repeat domain 14	TTC14	Homo sapiens (human)
151636	deltex E3 ubiquitin ligase 3L	DTX3L	Homo sapiens (human)
151742	protein phosphatase, Mg2+/Mn2+ dependent 1L	PPM1L	Homo sapiens (human)
151835	copine family member 9	CPNE9	Homo sapiens (human)
151887	coiled-coil domain containing 80	CCDC80	Homo sapiens (human)
151888	B and T lymphocyte associated	BTLA	Homo sapiens (human)
152002	xyloside xylosyltransferase 1	XXYLT1 Aliases: FLJ35155	Homo sapiens (human)	atrial fibrillation bronchus cancer bronchus carcinoma cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma nicotine dependence obesity osteoporosis
152137	coiled-coil domain containing 50	CCDC50	Homo sapiens (human)

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