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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 **390526 - 390550** of **393515** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
285362	sulfatase modifying factor 1	SUMF1 Aliases: FGE UNQ3037	Homo sapiens (human)	Balo concentric sclerosis Laron syndrome X-linked chondrodysplasia punctata 1 X-linked ichthyosis achondroplasia adrenoleukodystrophy autosomal dominant cerebellar ataxia autosomal dominant chondrodysplasia punctata autosomal recessive spinocerebellar ataxia 16 blindness breast cancer breast carcinoma cancer cataract central nervous system disease cerebral degeneration chondrodysplasia punctata chronic obstructive pulmonary disease communicating hydrocephalus cystic fibrosis embryoma epilepsy hydrocephalus ichthyosis inherited metabolic disorder intellectual disability learning disability lysosomal storage disease metachromatic leukodystrophy microcephaly mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis mucosulfatidosis multiple sclerosis narcolepsy obstructive hydrocephalus optic atrophy recurrent corneal erosion retinal degeneration rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 schizophrenia senile degeneration of brain sensorineural hearing loss visual epilepsy
285203	EGF domain specific O-linked N-acetylglucosamine transferase	EOGT Aliases: AER61 AER61 glycosyltransferase FLJ33770	Homo sapiens (human)	Adams-Oliver syndrome Clouston syndrome alopecia arteriovenous malformation autosomal recessive polycystic kidney disease cataract clubfoot communicating hydrocephalus epilepsy hydrocephalus hypertropia intellectual disability learning disability leukopenia mechanical strabismus microphthalmia obstructive hydrocephalus ophthalmoplegia periventricular leukomalacia polycystic kidney disease 4 portal hypertension primary pulmonary hypertension senile degeneration of brain strabismus tetralogy of Fallot thrombocytopenia visual epilepsy
284541	cytochrome P450 family 4 subfamily A member 22	CYP4A22	Homo sapiens (human)	autosomal recessive polycystic kidney disease hepatocellular carcinoma hypertension liver cancer polycystic kidney disease 4
284486	thioesterase superfamily member 5	THEM5 Aliases: FLJ37964	Homo sapiens (human)	catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia steatotic liver disease
284369	SIGLEC family like 1	SIGLECL1 Aliases: FLJ40235	Homo sapiens (human)
284348	LY6/PLAUR domain containing 5	LYPD5 Aliases: FLJ30469	Homo sapiens (human)	B-cell lymphoma Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adenocarcinoma adenoma basal cell carcinoma bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cervical adenocarcinoma cervical cancer cervix carcinoma childhood osteosarcoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common wart cribriform carcinoma diabetic ketoacidosis diffuse large B-cell lymphoma embryoma endometrial cancer endometrial carcinoma enterobiasis esophagus squamous cell carcinoma granular cell carcinoma hepatitis B hepatocellular carcinoma intestinal schistosomiasis large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma melanoma middle cerebral artery infarction nasopharynx carcinoma neuroblastoma nonpapillary renal cell carcinoma obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteosarcoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schistosomiasis sebaceous carcinoma skin melanoma squamous cell carcinoma squamous cell neoplasm stomach cancer stomach carcinoma sweat gland cancer tongue squamous cell carcinoma trichinosis 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 uterine corpus cancer varicocele
284266	sialic acid binding Ig like lectin 15	SIGLEC15 Aliases: HsT1361	Homo sapiens (human)	cancer embryoma osteoporosis
284194	galectin 9B	LGALS9B	Homo sapiens (human)
284161	glycerophosphodiester phosphodiesterase domain containing 1	GDPD1 Aliases: FLJ37451 GDE4	Homo sapiens (human)
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
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
283971	C-type lectin domain family 18 member C	CLEC18C Aliases: MGC34761	Homo sapiens (human)
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
283748	phospholipase A2 group IVD	PLA2G4D Aliases: cPLA2delta	Homo sapiens (human)	atopic dermatitis dermatitis hepatocellular carcinoma liver cancer mycosis fungoides schizophrenia
283578	transmembrane p24 trafficking protein family member 8	TMED8	Homo sapiens (human)
283464	glucoside xylosyltransferase 1	GXYLT1 Aliases: FLJ43151	Homo sapiens (human)
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
283417	dpy-19 like 2	DPY19L2 Aliases: FLJ32949 SPATA34 spermatogenesis associated 34	Homo sapiens (human)	azoospermia spermatogenic failure 9
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
283209	phosphoglucomutase 2 like 1	PGM2L1 Aliases: BM32A FLJ32029 glucose-1,6-bisphosphate synthase	Homo sapiens (human)
282969	fucose mutarotase	FUOM	Homo sapiens (human)
282873	acyl-CoA synthetase short chain family member 1	ACSS1	Bos taurus (cattle)
282870	cytochrome P450 family 1 subfamily A member 1	CYP1A1	Bos taurus (cattle)
282868	solute carrier family 2 (facilitated glucose/fructose transporter), member 5	SLC2A5	Bos taurus (cattle)
282867	solute carrier family 2 member 8	SLC2A8	Bos taurus (cattle)

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