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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 **7351 - 7375** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
9401	RecQ like helicase 4	RECQL4	Homo sapiens (human)
23164	myosin phosphatase Rho interacting protein	MPRIP	Homo sapiens (human)
10036	chromatin assembly factor 1 subunit A	CHAF1A	Homo sapiens (human)
4681	NBL1, DAN family BMP antagonist	NBL1	Homo sapiens (human)
5036	proliferation-associated 2G4	PA2G4	Homo sapiens (human)
5046	proprotein convertase subtilisin/kexin type 6	PCSK6	Homo sapiens (human)
79642	arylsulfatase family member J	ARSJ Aliases: FLJ23548	Homo sapiens (human)
220002	cytochrome b561 family member A3	CYB561A3	Homo sapiens (human)
80314	enhancer of polycomb homolog 1	EPC1	Homo sapiens (human)
4064	CD180 molecule	CD180	Homo sapiens (human)
5783	protein tyrosine phosphatase non-receptor type 13	PTPN13	Homo sapiens (human)
55573	CDV3 homolog	CDV3	Homo sapiens (human)
3029	hydroxyacylglutathione hydrolase	HAGH Aliases: GLO2 GLXII HAGH1	Homo sapiens (human)	Rett syndrome autism spectrum disorder autistic disorder autosomal dominant polycystic kidney disease cancer carcinoma clear cell adenocarcinoma inflammatory breast carcinoma kidney failure lung cancer lung non-small cell carcinoma polycystic kidney disease 1 prostate cancer prostate carcinoma rheumatoid arthritis sarcomatoid carcinoma schizophrenia uremia
114294	lactamase beta	LACTB	Homo sapiens (human)
29935	replication protein A4	RPA4	Homo sapiens (human)
80008	transmembrane protein 156	TMEM156	Homo sapiens (human)
28954	RRAD and GEM like GTPase 1	REM1	Homo sapiens (human)
27293	sphingomyelin phosphodiesterase acid like 3B	SMPDL3B Aliases: ASML3B	Homo sapiens (human)	Moyamoya disease focal segmental glomerulosclerosis glomerulonephritis kidney disease nephritis nephrosis pyoureter
1515	cathepsin V	CTSV	Homo sapiens (human)
133121	ectonucleotide pyrophosphatase/phosphodiesterase 6	ENPP6 Aliases: MGC33971	Homo sapiens (human)
9126	structural maintenance of chromosomes 3	SMC3 Aliases: BAM HCAP SMC3L1 bamacan bamacan proteoglycan	Homo sapiens (human)	Burkitt lymphoma Cockayne syndrome Cornelia de Lange syndrome 1 Cornelia de Lange syndrome 2 Cornelia de Lange syndrome 3 Cornelia de Lange syndrome Dubowitz syndrome Laron syndrome Marfan syndrome Meckel syndrome 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 Peters anomaly Prader-Willi syndrome Roberts syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Turner syndrome X-linked Aarskog syndrome achondroplasia acute myeloid leukemia adenocarcinoma adenoma adult lymphoma allergic asthma anxiety disorder arteriosclerotic cardiovascular disease asthma atherosclerosis 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 attention deficit hyperactivity disorder atypical chronic myeloid leukemia, BCR-ABL1 negative autistic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant polycystic kidney disease autosomal recessive Robinow syndrome blepharitis blind hypotensive eye bone cancer bone osteosarcoma bronchus cancer bronchus carcinoma cancer carcinoma cataract 32 multiple types cataract central nervous system lymphoma childhood lymphoma choanal atresia chondrodysplasia-pseudohermaphroditism syndrome chronic interstitial cystitis chronic monocytic leukemia cleft palate cleidocranial dysplasia clubfoot colon carcinoma colorectal cancer cone-rod dystrophy congenital diaphragmatic hernia congenital nystagmus congenital ptosis cornea plana coronary artery disease craniosynostosis cribriform carcinoma cryptorchidism dissociated nystagmus embryoma epilepsy esophagitis fundus albipunctatus gastroesophageal reflux disease generalized anxiety disorder gingivitis glaucoma gonadal dysgenesis granular cell carcinoma hepatocellular carcinoma humeroradial synostosis hydrocephalus hypertrichosis hypertropia hypospadias inguinal hernia intellectual disability interstitial cystitis intestinal benign neoplasm intestinal cancer intestinal volvulus intrinsic asthma isolated cleft palate kidney failure kwashiorkor large intestine cancer learning disability liver cancer lung benign neoplasm lung cancer lung carcinoma lymphoid leukemia lymphoma marasmus mechanical strabismus megacolon microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly myeloid leukemia myopia neuropathy nutrition disease obsolete SC phocomelia syndrome obsolete ymphosarcoma ophthalmoplegia osteosarcoma patent foramen ovale pathologic nystagmus peptic esophagitis periodontitis peripheral nervous system disease placental insufficiency pneumonia prostate cancer prostate carcinoma protein-energy malnutrition prune belly syndrome ptosis pulmonary valve stenosis pyloric stenosis radioulnar synostosis retinitis pigmentosa sarcomatoid carcinoma sensorineural hearing loss situs inversus speech disorder spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability 94 thromboangiitis obliterans toxic megacolon trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis tubular adenocarcinoma ventricular septal defect vesicoureteral reflux visual epilepsy
22985	apoptotic chromatin condensation inducer 1	ACIN1	Homo sapiens (human)
113622	ADP-ribosylhydrolase like 1	ADPRHL1	Homo sapiens (human)
29966	striatin 3	STRN3	Homo sapiens (human)
50506	dual oxidase 2	DUOX2	Homo sapiens (human)

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