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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	July 8, 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 **1476 - 1500** of **1582** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
253558	lysocardiolipin acyltransferase 1	LCLAT1 Aliases: 1ysophospholipid acyltransferase 6 AGPAT8 ALCAT1 FLJ37965 LPLAT6 acyl-CoA:lysocardiolipin acyltransferase 1	Homo sapiens (human)	dermatitis idiopathic interstitial pneumonia idiopathic pulmonary fibrosis pneumonia postinflammatory pulmonary fibrosis pulmonary fibrosis
253782	ceramide synthase 6	CERS6	Homo sapiens (human)	Kawasaki disease Kennedy's disease T-cell acute lymphoblastic leukemia acute lymphoblastic leukemia adult acute lymphocytic leukemia alcoholic hepatitis alcoholic liver cirrhosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer childhood acute lymphocytic leukemia chronic fatigue syndrome colitis colorectal cancer colorectal carcinoma diabetes mellitus disease of metabolism embryoma encephalitis encephalomyelitis gastroenteritis glucose intolerance head and neck squamous cell carcinoma hematologic cancer idiopathic scoliosis ileitis ileocolitis large intestine cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma melanoma mitochondrial metabolism disease mitochondrial myopathy multiple sclerosis myelitis obesity prediabetes syndrome skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma substance abuse substance-related disorder tongue squamous cell carcinoma type 2 diabetes mellitus
254531	lysophosphatidylcholine acyltransferase 4	LPCAT4 Aliases: FLJ10257 LPAAT-eta LPEAT2 LPLAT10 lysophosphatidylethanolamine acyltransferase 2 lysophospholipid acyltransferase 10	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
254773	lysozyme g2	LYG2 Aliases: LYGA2 LYGH	Homo sapiens (human)
255043	transmembrane protein 86B	TMEM86B Aliases: MGC30208 alkenylglycerophosphocholine hydrolase alkenylglycerophosphoethanolamine hydrolase	Homo sapiens (human)
255189	phospholipase A2 group IVF	PLA2G4F Aliases: PLA2G4F/Z	Homo sapiens (human)	arthritis arthropathy osteoarthritis
256356	glycerol kinase 5	GK5	Homo sapiens (human)
256435	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 3	ST6GALNAC3 Aliases: ST6GALNAC III	Homo sapiens (human)	diabetes mellitus gestational diabetes idiopathic scoliosis prostate cancer prostate carcinoma type 2 diabetes mellitus
256710	GLIPR1 like 1	GLIPR1L1 Aliases: MGC26856	Homo sapiens (human)
257202	glutathione peroxidase 6	GPX6 Aliases: selenoprotein GPX6	Homo sapiens (human)	Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease breast cancer depressive disorder lung squamous cell carcinoma major depressive disorder melancholic depression obsolete melancholia ovarian cancer ovarian carcinoma
259230	sphingomyelin synthase 1	SGMS1 Aliases: MGC17342 MOB SMS1 phosphatidylcholine:ceramide cholinephosphotransferase 1	Homo sapiens (human)	St. Louis encephalitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bronchus cancer bronchus carcinoma cancer central nervous system cancer cholangiocarcinoma colorectal cancer colorectal carcinoma diabetes mellitus embryoma giant cell glioblastoma glioblastoma gliosarcoma hepatitis A hepatitis high grade glioma intrahepatic cholangiocarcinoma large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus melanoma mixed glioma pancreatic cancer pancreatic carcinoma pulmonary edema skin melanoma systemic lupus erythematosus type 2 diabetes mellitus
266722	heparan sulfate 6-O-sulfotransferase 3	HS6ST3	Homo sapiens (human)	Balo concentric sclerosis adrenoleukodystrophy breast cancer breast carcinoma cancer central nervous system disease diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy hepatitis B narcolepsy nicotine dependence obesity type 2 diabetes mellitus
266727	MAM domain containing glycosylphosphatidylinositol anchor 1	MDGA1 Aliases: GPIM MAMDC3	Homo sapiens (human)	Kawasaki disease bipolar disorder cancer depressive disorder major depressive disorder melancholic depression neurotic disorder obsolete melancholia schizophrenia
282969	fucose mutarotase	FUOM	Homo sapiens (human)
283209	phosphoglucomutase 2 like 1	PGM2L1 Aliases: BM32A FLJ32029 glucose-1,6-bisphosphate synthase	Homo sapiens (human)
283358	beta-1,4-N-acetyl-galactosaminyltransferase 3	B4GALNT3 Aliases: B4GalNac-T3 FLJ16224 FLJ40362	Homo sapiens (human)	arthritis arthropathy cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma embryoma idiopathic scoliosis large intestine cancer osteoarthritis ovarian cancer papillary adenocarcinoma papillary renal cell carcinoma thyroid gland papillary carcinoma
283417	dpy-19 like 2	DPY19L2 Aliases: FLJ32949 SPATA34 spermatogenesis associated 34	Homo sapiens (human)	azoospermia spermatogenic failure 9
283420	C-type lectin domain containing 9A	CLEC9A Aliases: CD370 DNGR-1 HEEE9341 UNQ9341	Homo sapiens (human)	acquired immunodeficiency syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer coronary artery disease herpes simplex human immunodeficiency virus infectious disease influenza leprosy pneumonia primary immunodeficiency disease tuberculosis viral infectious disease
283464	glucoside xylosyltransferase 1	GXYLT1 Aliases: FLJ43151	Homo sapiens (human)
283578	transmembrane p24 trafficking protein family member 8	TMED8	Homo sapiens (human)
283748	phospholipase A2 group IVD	PLA2G4D Aliases: cPLA2delta	Homo sapiens (human)	atopic dermatitis dermatitis hepatocellular carcinoma liver cancer mycosis fungoides schizophrenia
283871	phosphoglycolate phosphatase	PGP	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 Ewing sarcoma Hirschsprung's disease Krukenberg carcinoma Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome acute lymphoblastic leukemia acute myeloid leukemia adenocarcinoma adenoma allergic asthma alternating hemiplegia of childhood asthma autonomic neuropathy autosomal dominant polycystic kidney disease basal cell carcinoma bipolar disorder bone marrow disease brain ischemia breast cancer breast carcinoma cancer carcinoma central nervous system disease central nervous system lymphoma cerebral degeneration childhood leukemia chorioamnionitis chronic myeloid leukemia colon adenocarcinoma colorectal cancer colorectal carcinoma cribriform carcinoma degenerative disc disease depressive disorder diabetes mellitus diabetic ketoacidosis disease of metabolism dysthymic disorder embryoma erythromelalgia essential hypertension essential thrombocythemia familial retinoblastoma glucose intolerance granular cell carcinoma hepatocellular carcinoma hypertension inflammatory bowel disease intrinsic asthma kidney cancer large intestine cancer leukemia lingual-facial-buccal dyskinesia liver cancer lung benign neoplasm lung carcinoma lymphoid leukemia lymphoma major depressive disorder melancholic depression myelodysplastic syndrome myeloid leukemia myotonic dystrophy type 1 myotonic dystrophy type 2 nervous system disease neuroblastoma neurodegenerative disease neuroectodermal tumor neuropathy neurotic disorder obsolete major affective disorder 2 obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma peripheral nervous system disease polycystic kidney disease 1 polyneuropathy prediabetes syndrome retinoblastoma rhabdomyosarcoma rhinitis schizophrenia sebaceous carcinoma sexual dysfunction squamous cell carcinoma sweat gland cancer tongue squamous cell carcinoma trilateral retinoblastoma 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 varicose veins vitiligo
283971	C-type lectin domain family 18 member C	CLEC18C Aliases: MGC34761	Homo sapiens (human)
284004	hexosaminidase D	HEXD Aliases: FLJ23825 hexosaminidase D, cytosolic	Homo sapiens (human)	GM2 gangliosidosis Gilles de la Tourette syndrome Marfan syndrome Sandhoff disease Tay-Sachs disease Timothy syndrome dystonia lingual-facial-buccal dyskinesia long QT syndrome 8 situs inversus tricuspid valve stenosis tuberous sclerosis 1 tuberous sclerosis
284098	phosphatidylinositol glycan anchor biosynthesis class W	PIGW Aliases: FLJ37433 GPI-anchored wall protein transfer 1 homolog (S. cerevisiae) Gwt1 PIG-W	Homo sapiens (human)	Cogan syndrome Hirschsprung's disease Unverricht-Lundborg syndrome West syndrome alternating hemiplegia of childhood autonomic neuropathy blepharospasm capillary disease central nervous system disease congenital diaphragmatic hernia craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy epilepsy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia hyperphosphatasia with impaired intellectual development syndrome 5 intellectual disability learning disability monocular esotropia nervous system disease obsolete infantile epileptic encephalopathy oligohydramnios pneumonia scoliosis syndromic X-linked intellectual disability 94 telangiectasis visual epilepsy

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