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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 **421926 - 421950** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
1386	activating transcription factor 2	ATF2	Homo sapiens (human)
1385	cAMP responsive element binding protein 1	CREB1	Homo sapiens (human)
1384	carnitine O-acetyltransferase	CRAT	Homo sapiens (human)
1380	complement C3d receptor 2	CR2	Homo sapiens (human)
1379	complement C3b/C4b receptor 1 like	CR1L	Homo sapiens (human)
1378	complement C3b/C4b receptor 1 (Knops blood group)	CR1	Homo sapiens (human)
1376	carnitine palmitoyltransferase 2	CPT2 Aliases: CPTASE	Homo sapiens (human)	Chanarin-Dorfman syndrome Meckel syndrome Pearson syndrome Reye syndrome X-linked dilated cardiomyopathy abdominal obesity-metabolic syndrome 1 acute myocardial infarction arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis attention deficit hyperactivity disorder autosomal dominant polycystic kidney disease beta thalassemia brain disease brain edema breast cancer breast carcinoma cancer carcinoma cardiomyopathy carnitine palmitoyltransferase I deficiency carnitine palmitoyltransferase II deficiency cataract chronic fatigue syndrome chronic kidney disease clubfoot colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy disease of metabolism embryoma encephalitis encephalomyelitis endomyocardial fibrosis epilepsy essential thrombocythemia familial hyperlipidemia familial periodic paralysis fibromyalgia glycogen storage disease II glycogen storage disease V hepatitis C hepatitis hepatocellular carcinoma hydrocephalus hydronephrosis hyperglycemia hypertrophic cardiomyopathy hypoglycemia influenza isolated elevated serum creatine phosphokinase levels kidney failure large intestine cancer lipid metabolism disorder liver cancer liver cirrhosis medium chain acyl-CoA dehydrogenase deficiency microcephaly mitochondrial metabolism disease mitochondrial myopathy mitochondrial trifunctional protein deficiency multiple acyl-CoA dehydrogenase deficiency muscular disease myelitis myelodysplastic syndrome myocardial infarction myoglobinuria myopathy myositis neurogenic arthropathy neuroleptic malignant syndrome obesity ovarian cancer pancytopenia placental insufficiency polycystic ovary syndrome primary pulmonary hypertension prostate cancer prostate carcinoma pseudosarcomatous fibromatosis psoriatic arthritis sarcomatoid carcinoma sick sinus syndrome silent myocardial infarction status epilepticus steatotic liver disease systemic primary carnitine deficiency disease thalassemia type 2 diabetes mellitus urea cycle disorder very long chain acyl-CoA dehydrogenase deficiency viral infectious disease visual epilepsy
1375	carnitine palmitoyltransferase 1B	CPT1B Aliases: CPT1-M M-CPT1 carnitine O-palmitoyltransferase 1B	Homo sapiens (human)	Balo concentric sclerosis Down syndrome Pearson syndrome acute myocardial infarction adrenoleukodystrophy bladder carcinoma cancer central nervous system disease chronic recurrent multifocal osteomyelitis colitis congestive heart failure coronary thrombosis embryoma gastroenteritis hepatitis hepatocellular carcinoma ileitis ileocolitis liver cancer morbid obesity myocardial infarction narcolepsy post-traumatic stress disorder restless legs syndrome silent myocardial infarction steatotic liver disease systemic primary carnitine deficiency disease urinary bladder cancer very long chain acyl-CoA dehydrogenase deficiency
1374	carnitine palmitoyltransferase 1A	CPT1A Aliases: CPT1-L L-CPT1	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 D-bifunctional protein deficiency Niemann-Pick disease type C1 Niemann-Pick disease Pearson syndrome Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myeloid leukemia acute myocardial infarction alcoholic hepatitis alveolar rhabdomyosarcoma amnestic disorder beta thalassemia breast cancer breast carcinoma cancer carcinoma cardiomyopathy carnitine palmitoyltransferase I deficiency cataract 4 multiple types cerebral degeneration chronic fatigue syndrome chronic kidney disease colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysthymic disorder embryoma encephalitis encephalomyelitis end stage renal disease endomyocardial fibrosis epilepsy esophagus squamous cell carcinoma essential thrombocythemia familial hyperlipidemia familial hypertrophic cardiomyopathy giant cell glioblastoma glioblastoma hepatitis C hepatitis hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinism hypertrophic cardiomyopathy hypoglycemia inflammatory bowel disease isolated elevated serum creatine phosphokinase levels large intestine cancer lipid metabolism disorder liver cancer liver carcinoma liver cirrhosis lymphangioleiomyomatosis major depressive disorder medium chain acyl-CoA dehydrogenase deficiency melancholic depression melanoma metabolic dysfunction-associated steatohepatitis mitochondrial trifunctional protein deficiency multiple acyl-CoA dehydrogenase deficiency multiple sclerosis myelitis myelodysplastic syndrome myocardial infarction nasopharynx carcinoma neurotic disorder obesity obsolete melancholia osteoporosis placental insufficiency polycystic ovary syndrome primary pulmonary hypertension prostate cancer prostate carcinoma psoriatic arthritis renal tubular acidosis retrograde amnesia sarcomatoid carcinoma sick sinus syndrome silent myocardial infarction skin melanoma speech disorder steatotic liver disease stomach cancer stomach carcinoma sudden infant death syndrome systemic primary carnitine deficiency disease thalassemia type 2 diabetes mellitus urea cycle disorder very long chain acyl-CoA dehydrogenase deficiency visual epilepsy
1373	carbamoyl-phosphate synthase 1	CPS1	Homo sapiens (human)
1371	coproporphyrinogen oxidase	CPOX	Homo sapiens (human)
1370	carboxypeptidase N subunit 2	CPN2	Homo sapiens (human)
1369	carboxypeptidase N subunit 1	CPN1	Homo sapiens (human)
1368	carboxypeptidase M	CPM Aliases: renal carboxypeptidase urinary carboxypeptidase B	Homo sapiens (human)	adult liposarcoma anthracosilicosis anxiety disorder aphasia asbestosis atrial fibrillation breast cancer breast carcinoma cancer childhood liposarcoma colorectal cancer colorectal carcinoma embryoma endometriosis of ovary endometriosis generalized anxiety disorder inflammatory liposarcoma kidney failure large intestine cancer lipoma liposarcoma lung adenocarcinoma lung cancer multiple symmetric lipomatosis pleomorphic lipoma pleomorphic liposarcoma proliferative diabetic retinopathy sclerosing liposarcoma silicosis well-differentiated liposarcoma
1363	carboxypeptidase E	CPE	Homo sapiens (human)
1362	carboxypeptidase D	CPD	Homo sapiens (human)
1361	carboxypeptidase B2	CPB2	Homo sapiens (human)
1359	carboxypeptidase A3	CPA3	Homo sapiens (human)
1356	ceruloplasmin	CP	Homo sapiens (human)
1353	cytochrome c oxidase copper chaperone COX11	COX11	Homo sapiens (human)
1317	solute carrier family 31 member 1	SLC31A1	Homo sapiens (human)
1314	COPI coat complex subunit alpha	COPA	Homo sapiens (human)
1312	catechol-O-methyltransferase	COMT	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 B-cell lymphoma Balo concentric sclerosis Clostridium difficile colitis Cockayne syndrome DiGeorge syndrome Dowling-Degos disease Down syndrome Gilles de la Tourette syndrome Graves' disease Hirschsprung's disease Horner's syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Kleine-Levin syndrome Langerhans-cell histiocytosis Laron syndrome Lewy body dementia Lynch syndrome Meckel syndrome Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Parkinsonism Pick's disease Reye syndrome Wernicke-Korsakoff syndrome Wolfram syndrome 1 Wolfram syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acne acquired immunodeficiency syndrome acrodermatitis acute myocardial infarction adenocarcinoma adenoma adrenal gland cancer adrenoleukodystrophy adult lymphoma agnosia alcohol dependence alcohol use disorder alexia allergic asthma alternating hemiplegia of childhood amnestic disorder amphetamine abuse androgen insensitivity syndrome anencephaly anorexia nervosa antisocial personality disorder anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy 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 autism spectrum disorder autistic disorder autonomic neuropathy autosomal dominant polycystic kidney disease avoidant personality disorder bipolar disorder bladder carcinoma borderline personality disorder breast cancer breast carcinoma breast fibrocystic disease bronchus cancer bronchus carcinoma bulimia nervosa bullous congenital ichthyosiform erythroderma cancer cannabis abuse cannabis dependence cardiovascular system disease carpal tunnel syndrome cataract central nervous system disease central nervous system lymphoma central nervous system origin vertigo central sleep apnea cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood disintegrative disease childhood kidney cell carcinoma childhood lymphoma choanal atresia cholecystolithiasis choledocholithiasis cholelithiasis chromophobe renal cell carcinoma chromosome 17p13.1 deletion syndrome chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma cleft palate clubfoot cocaine abuse cocaine dependence cognitive disorder collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma communicating hydrocephalus conduct disorder congenital diarrhea 5 with tufting enteropathy congenital hypothyroidism congenital ptosis conversion disorder corneal neovascularization coronary artery disease coronary thrombosis craniosynostosis cribriform carcinoma critical illness polyneuropathy cryptorchidism degenerative disc disease delusional disorder dementia dental caries dental fluorosis dentin caries depressive disorder desquamative interstitial pneumonia diabetes mellitus diabetic ketoacidosis diarrhea disease of mental health dissociative disorder distal myopathy double outlet right ventricle drug dependence drug psychosis duodenum cancer dyslexia dysthymic disorder dystonia eating disorder eclampsia embryoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis epilepsy episodic kinesigenic dyskinesia 1 episodic kinesigenic dyskinesia 2 esophagitis esophagus squamous cell carcinoma essential hypertension eumycotic mycetoma female breast carcinoma fibrodysplasia ossificans progressiva fibromyalgia gallbladder disease gastroesophageal reflux disease generalized anxiety disorder glaucoma glucose intolerance granular cell carcinoma head and neck squamous cell carcinoma heart cancer heart disease hepatitis C hepatocellular carcinoma heroin dependence herpes simplex holoprosencephaly 1 holoprosencephaly human immunodeficiency virus infectious disease hydrocephalus hypercalcemia hypertension hypertensive encephalopathy hyperthyroidism hypertropia hypoparathyroidism hypospadias hypothyroidism imperforate anus impulse control disorder inappropriate ADH syndrome inflammatory and toxic neuropathy inguinal hernia intellectual disability intermittent explosive disorder intrinsic asthma irritable bowel syndrome isolated cleft palate kidney cancer kleptomania large intestine cancer late onset Parkinson's disease lateral meningocele syndrome learning disability leiomyoma lingual-facial-buccal dyskinesia lissencephaly liver cancer liver carcinoma liver disease lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder male infertility mechanical strabismus melancholic depression meningoencephalitis microcephaly microglandular adenosis microphthalmia migraine without aura migraine mitral valve stenosis mood disorder morphine dependence multiple sclerosis myelitis myelomeningocele myeloproliferative disorder with eosinophilia myocardial infarction myofibroma myositis ossificans myositis myxedema narcissistic personality disorder narcolepsy neonatal abstinence syndrome nephrocalcinosis nervous system disease neuroblastoma neurocirculatory asthenia neurodegenerative disease neuropathy neurotic disorder nicotine dependence nodular prostate non-Hodgkin lymphoma nutmeg liver obesity obsessive-compulsive disorder obsessive-compulsive personality disorder obsolete T-cell lymphoblastic leukemia/lymphoma obsolete constipation obsolete dyspepsia obsolete major affective disorder 1 obsolete major affective disorder 2 obsolete melancholia obsolete ymphosarcoma obstructive hydrocephalus obstructive sleep apnea omphalocele ophthalmoplegia opiate dependence optic atrophy osteoarthritis osteochondritis dissecans osteoporosis otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma panic disorder papillary renal cell carcinoma paranoid schizophrenia parapsoriasis patent ductus arteriosus patent foramen ovale pathological gambling peptic esophagitis peripheral nervous system disease pheochromocytoma phobic disorder phosphorus metabolism disease placental insufficiency polycystic ovary syndrome polyhydramnios polyneuropathy post-traumatic stress disorder pre-eclampsia prediabetes syndrome premature ejaculation premature menopause primary immunodeficiency disease primary ovarian insufficiency progressive pseudorheumatoid arthropathy of childhood prostate cancer prostate carcinoma prostatic adenoma pseudohypoparathyroidism psoriasis psychotic disorder ptosis purpura pustulosis of palm and sole rectal benign neoplasm rectum adenocarcinoma rectum cancer recurrent hypersomnia renal carcinoma renal cell carcinoma renal hypoplasia reticulate acropigmentation of Kitamura reticulosarcoma retrograde amnesia rumination disorder sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder schizotypal personality disorder scoliosis seasonal affective disorder seborrheic dermatitis seborrheic infantile dermatitis seborrheic keratosis secondary Parkinson disease senile degeneration of brain sickle cell anemia silent myocardial infarction small intestine cancer social phobia somatization disorder somatoform disorder spina bifida sporadic breast cancer squamous cell carcinoma stomach cancer stomach carcinoma strabismus subacute delirium substance abuse substance-related disorder systemic lupus erythematosus tethered spinal cord syndrome tetralogy of Fallot thrombocytopenia thrombophilia thyrotoxicosis tibial muscular dystrophy tongue squamous cell carcinoma transient myeloproliferative syndrome tricuspid atresia tubular adenocarcinoma type 2 diabetes mellitus umbilical hernia uremia urinary bladder cancer urinary system benign neoplasm urinary system cancer uterine corpus cancer uterine fibroid varicose veins velocardiofacial syndrome ventricular septal defect vesicoureteral reflux visual epilepsy vitiligo withdrawal disorder xeroderma pigmentosum group A xeroderma pigmentosum group B xeroderma pigmentosum group C xeroderma pigmentosum group D xeroderma pigmentosum group E xeroderma pigmentosum group F xeroderma pigmentosum group G xeroderma pigmentosum variant type xeroderma pigmentosum
1311	cartilage oligomeric matrix protein	COMP	Homo sapiens (human)
1310	collagen type XIX alpha 1 chain	COL19A1	Homo sapiens (human)

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