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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 **6301 - 6325** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
347051	solute carrier family 10 member 5	SLC10A5	Homo sapiens (human)
23236	phospholipase C beta 1	PLCB1 Aliases: KIAA0581 PLC-I PLC154 phosphoinositide phospholipase C	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 Chagas disease Hirschsprung's disease Kawasaki disease Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Miller-Dieker lissencephaly syndrome Pick's disease Reye syndrome Unverricht-Lundborg syndrome West syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult oligodendroglioma amyotrophic lateral sclerosis anaplastic astrocytoma autism spectrum disorder autistic disorder benign epilepsy with centrotemporal spikes bipolar disorder blepharospasm brain disease breast cancer breast carcinoma cancer cardiovascular system disease central nervous system cancer cerebral degeneration childhood cerebral astrocytoma childhood oligodendroglioma chromosome 17p13.1 deletion syndrome colon adenocarcinoma colon cancer colonic benign neoplasm colorectal cancer coronary aneurysm coronary thrombosis cribriform carcinoma depressive disorder developmental and epileptic encephalopathy 12 developmental and epileptic encephalopathy 1 diabetes mellitus diabetic ketoacidosis early infantile epileptic encephalopathy early myoclonic encephalopathy endometriosis of uterus endometriosis epilepsy essential thrombocythemia fibrillary astrocytoma focal epilepsy focal hand dystonia gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance granular cell carcinoma heart disease hepatocellular carcinoma high grade glioma infertility juvenile pilocytic astrocytoma large intestine cancer lissencephaly liver cancer major depressive disorder malignant astrocytoma melancholic depression mixed glioma mixed oligodendroglioma-astrocytoma mood disorder myelodysplastic syndrome myocardial infarction myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 neuroblastoma neurotic disorder nicotine dependence obesity obsolete infantile epileptic encephalopathy obsolete melancholia obstructive sleep apnea oligodendroglioma partial motor epilepsy pilocytic astrocytoma poikiloderma with neutropenia prediabetes syndrome primary biliary cholangitis progressive muscular atrophy protoplasmic astrocytoma schizophrenia silent myocardial infarction subependymal giant cell astrocytoma substance abuse substance-related disorder trypanosomiasis tubular adenocarcinoma visual epilepsy
3485	insulin like growth factor binding protein 2	IGFBP2	Homo sapiens (human)
81611	acidic nuclear phosphoprotein 32 family member E	ANP32E	Homo sapiens (human)
80024	solute carrier family 8 member B1	SLC8B1	Homo sapiens (human)
3615	inosine monophosphate dehydrogenase 2	IMPDH2	Homo sapiens (human)
3213	homeobox B3	HOXB3	Homo sapiens (human)
729201	sperm acrosome associated 5B	SPACA5B Aliases: LYZL5B	Homo sapiens (human)
11285	beta-1,4-galactosyltransferase 7	B4GALT7 Aliases: XGALT-1 beta4Gal-T7 galactosyltransferase I	Homo sapiens (human)	Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome Hailey-Hailey disease IgA glomerulonephritis Laron syndrome Larsen-like syndrome B3GAT3 type Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Rothmund-Thomson syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome achondroplasia aortic valve disease 2 aortic valve stenosis arthritis arthropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive Robinow syndrome 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 bone disease cartilage disease chondrodysplasia-pseudohermaphroditism syndrome cleidocranial dysplasia clubfoot colitis collagen disease coloboma congenital disorder of glycosylation type IId congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 connective tissue disease cryptorchidism cutis laxa enophthalmos gastroenteritis gingivitis hepatocellular carcinoma humeroradial synostosis ileitis ileocolitis lipoatrophic diabetes mellitus lipodystrophy liver cancer mal de Meleda microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II mucopolysaccharidosis IV multiple epiphyseal dysplasia obsolete exophthalmos orbital disease osteoarthritis osteochondrodysplasia osteogenesis imperfecta pulmonary valve stenosis radioulnar synostosis restrictive dermopathy rheumatoid arthritis scoliosis skin disease spermatic cord torsion trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
26001	ring finger protein 167	RNF167	Homo sapiens (human)
8341	H2B clustered histone 15	H2BC15	Homo sapiens (human)
23556	phosphatidylinositol glycan anchor biosynthesis class N	PIGN Aliases: GPI ethanolamine phosphate transferase 1 MCD4 PIG-N	Homo sapiens (human)	Dandy-Walker syndrome Hirschsprung's disease Marfan syndrome Meckel syndrome Miller-Dieker lissencephaly syndrome Paget's disease of bone acute monocytic leukemia acute myeloid leukemia amblyopia atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal dominant polycystic kidney disease basal ganglia disease blepharitis blepharospasm cerebral degeneration chromosome 17p13.1 deletion syndrome chronic recurrent multifocal osteomyelitis cleft palate colorectal cancer colorectal carcinoma congenital diaphragmatic hernia congenital nystagmus cryptorchidism dissociated nystagmus duodenal atresia epilepsy esophagitis esotropia essential thrombocythemia focal hand dystonia gastroesophageal reflux disease gingival hypertrophy gingival overgrowth heart septal defect holoprosencephaly 1 holoprosencephaly hydrocephalus hydronephrosis hypospadias idiopathic interstitial pneumonia imperforate anus intellectual disability isolated cleft palate large intestine cancer learning disability lingual-facial-buccal dyskinesia lissencephaly lung adenocarcinoma lung cancer mammary Paget's disease microphthalmia monocular esotropia movement disease multiple congenital anomalies-hypotonia-seizures syndrome 1 myelodysplastic syndrome omphalocele patent ductus arteriosus patent foramen ovale pathologic nystagmus peptic esophagitis polyhydramnios postinflammatory pulmonary fibrosis primary pulmonary hypertension pulmonary fibrosis recurrent corneal erosion renal agenesis situs inversus spontaneous ocular nystagmus strabismic amblyopia tetralogy of Fallot tuberous sclerosis umbilical hernia vesicoureteral reflux visual epilepsy
51194	importin 11	IPO11	Homo sapiens (human)
346606	monoacylglycerol O-acyltransferase 3	MOGAT3 Aliases: DC7 DGAT2L2 MGAT3	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 Pick's disease Reye syndrome cerebral degeneration steatotic liver disease
30011	SH3 domain containing kinase binding protein 1	SH3KBP1	Homo sapiens (human)
26000	TBC1 domain family member 10B	TBC1D10B	Homo sapiens (human)
7011	telomerase associated protein 1	TEP1	Homo sapiens (human)
22795	nidogen 2	NID2	Homo sapiens (human)
51614	ERGIC and golgi 3	ERGIC3	Homo sapiens (human)
10446	leucine rich repeat neuronal 2	LRRN2	Homo sapiens (human)
84725	pleckstrin homology domain containing A8	PLEKHA8 Aliases: FAPP2 MGC3358	Homo sapiens (human)	breast cancer breast carcinoma cancer central nervous system cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer embryoma gliosarcoma high grade glioma large intestine cancer mixed glioma
133418	embigin	EMB	Homo sapiens (human)
6938	transcription factor 12	TCF12	Homo sapiens (human)
100506581	chromosome 16 open reading frame 95	C16orf95	Homo sapiens (human)
57455	RNA exonuclease 1 homolog	REXO1	Homo sapiens (human)

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