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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 **6651 - 6675** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
2814	glycoprotein V platelet	GP5	Homo sapiens (human)
2813	glycoprotein 2	GP2 Aliases: ZAP75	Homo sapiens (human)	Crohn's colitis Crohn's disease Ebola hemorrhagic fever acute myeloid leukemia classic galactosemia galactokinase deficiency galactosemia gallbladder disease gastroenteritis gastrointestinal system disease hepatitis C herpes zoster inflammatory bowel disease 1 inflammatory bowel disease intestinal disease liver disease microphthalmia obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma proctitis ulcerative colitis
2812	glycoprotein Ib platelet subunit beta	GP1BB	Homo sapiens (human)
2811	glycoprotein Ib platelet subunit alpha	GP1BA	Homo sapiens (human)
2805	glutamic-oxaloacetic transaminase 1	GOT1	Homo sapiens (human)	amyloidosis amyotrophic lateral sclerosis cardiomyopathy pancreatic ductal adenocarcinoma transient cerebral ischemia
26003	golgi reassembly stacking protein 2	GORASP2	Homo sapiens (human)
54856	gon-4 like	GON4L	Homo sapiens (human)
64083	golgi phosphoprotein 3	GOLPH3 Aliases: GOPP1 GPP34 MIDAS Vps74 coat-protein golgi peripheral membrane protein 1, 34 kDa golgi protein golgi-associated protein	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 Barrett's esophagus Glanzmann's thrombasthenia Hermansky-Pudlak syndrome 2 Japanese encephalitis Lyme disease Pick's disease Reye syndrome X-linked dyskeratosis congenita alternating hemiplegia of childhood anaplastic astrocytoma ankyloblepharon-ectodermal defects-cleft lip/palate syndrome anxiety disorder autonomic neuropathy bladder carcinoma blood coagulation disease breast cancer breast carcinoma breast fibroadenoma bronchus cancer bronchus carcinoma cancer carcinoma catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia central nervous system cancer central nervous system disease cerebral degeneration chikungunya childhood astrocytic tumor childhood cerebral astrocytoma childhood germ cell cancer cholera chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation cystadenoma dengue disease dengue hemorrhagic fever depressive disorder dyskeratosis congenita dysplastic nevus syndrome dysthymic disorder embryoma embryonal cancer endometrial cancer endometrial carcinoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension fibrillary astrocytoma fibromyalgia gallbladder disease gemistocytic astrocytoma generalized anxiety disorder germ cell and embryonal cancer germ cell cancer germinoma giant cell glioblastoma glioblastoma gliosarcoma gray platelet syndrome hematopoietic system disease hepatitis A hepatitis B hepatitis C hepatocellular carcinoma high grade glioma hypertension hypochromic anemia hypohidrotic ectodermal dysplasia influenza juvenile pilocytic astrocytoma large intestine cancer liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma major depressive disorder malaria malignant astrocytoma melancholic depression melanoma microphthalmia migraine mixed glioma mucinous adenocarcinoma nervous system disease neuroblastoma neurotic disorder nodular prostate nonpapillary renal cell carcinoma obsolete Matthew-Wood syndrome obsolete inherited blood coagulation disease obsolete melancholia ovarian cancer ovarian carcinoma pancreatic ductal adenocarcinoma papillary renal cell carcinoma papilloma phobic disorder pilocytic astrocytoma platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma qualitative platelet defect renal carcinoma renal cell carcinoma rhabdomyosarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma skin melanoma spinal stenosis squamous cell papilloma stomach cancer stomach carcinoma subependymal giant cell astrocytoma tongue cancer urinary bladder cancer uterine corpus cancer viral infectious disease yellow fever
113201	golgi membrane protein 2	GOLM2	Homo sapiens (human)
51280	golgi membrane protein 1	GOLM1	Homo sapiens (human)
27333	golgi integral membrane protein 4	GOLIM4	Homo sapiens (human)
2804	golgin B1	GOLGB1	Homo sapiens (human)
440270	golgin A8 family member B	GOLGA8B	Homo sapiens (human)
23015	golgin A8 family member A	GOLGA8A	Homo sapiens (human)
727832	golgin A6 family like 6 (gene/pseudogene)	GOLGA6L6	Homo sapiens (human)
283685	golgin A6 family like 2	GOLGA6L2	Homo sapiens (human)
283767	golgin A6 family like 1	GOLGA6L1	Homo sapiens (human)
2803	golgin A4	GOLGA4	Homo sapiens (human)
2802	golgin A3	GOLGA3	Homo sapiens (human)
2801	golgin A2	GOLGA2	Homo sapiens (human)
2799	glucosamine (N-acetyl)-6-sulfatase	GNS Aliases: N-acetylglucosamine-6-sulfatase Sanfilippo disease IIID	Homo sapiens (human)	brain cancer cancer diarrhea epilepsy fundus dystrophy hypertrichosis hypertrophic cardiomyopathy 1 intellectual disability learning disability low tension glaucoma lysosomal storage disease melanoma mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis rheumatoid arthritis sensorineural hearing loss skin melanoma visual epilepsy
2798	gonadotropin releasing hormone receptor	GNRHR	Homo sapiens (human)
84572	N-acetylglucosamine-1-phosphate transferase subunit gamma	GNPTG Aliases: CAB56184 GlcNAc-phosphotransferase gamma-subunit c316G12.3	Homo sapiens (human)	Fabry disease Laron syndrome achondroplasia alexia aortic valve disease 2 aortic valve insufficiency aortic valve stenosis chylomicron retention disease cone-rod dystrophy dyslexia fundus albipunctatus glycoproteinosis lipid storage disease lysosomal storage disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucolipidosis III gamma mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis myopia osteochondrodysplasia retinitis pigmentosa scoliosis stuttering
79158	N-acetylglucosamine-1-phosphate transferase subunits alpha and beta	GNPTAB Aliases: KIAA1208 MGC4170	Homo sapiens (human)	Ebola hemorrhagic fever Fabry disease Laron syndrome Legg-Calve-Perthes disease Scheuermann's disease achondroplasia alexia anemia aortic valve insufficiency arrhythmogenic right ventricular cardiomyopathy autistic disorder cancer capillary hemangioma cardiomyopathy cavernous hemangioma chromophobe renal cell carcinoma chylomicron retention disease clear cell renal cell carcinoma clubfoot collecting duct carcinoma congenital central hypoventilation syndrome congestive heart failure corneal dystrophy craniosynostosis disease of metabolism dyslexia embryoma endomyocardial fibrosis enterocele familial hypertrophic cardiomyopathy glycoproteinosis hemangioma hypertrophic cardiomyopathy inguinal hernia intellectual disability keratosis follicularis learning disability lipid storage disease lysosomal storage disease macrocytic anemia megalocornea mixed sleep apnea mongolian spot mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucolipidosis mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis multiple epiphyseal dysplasia nonpapillary renal cell carcinoma obstructive sleep apnea omphalocele osteochondrodysplasia papillary renal cell carcinoma pseudoxanthoma elasticum renal carcinoma renal cell carcinoma retinal degeneration retinal disease retinitis sarcomatoid renal cell carcinoma scoliosis sleep apnea spinal cord disease stuttering syringomyelia umbilical hernia
64841	glucosamine-phosphate N-acetyltransferase 1	GNPNAT1 Aliases: FLJ10607 Gpnat1	Homo sapiens (human)	cancer diabetes mellitus diabetic ketoacidosis keratosis follicularis spinulosa decalvans type 2 diabetes mellitus

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