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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 **422376 - 422400** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
391	ras homolog family member G	RHOG	Homo sapiens (human)
389	ras homolog family member C	RHOC	Homo sapiens (human)
388	ras homolog family member B	RHOB	Homo sapiens (human)
387	ras homolog family member A	RHOA Aliases: RHOH12 Rho12	Homo sapiens (human)
378	ARF GTPase 4	ARF4	Homo sapiens (human)	Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome autosomal dominant polycystic kidney disease breast cancer cystic kidney disease giant cell glioblastoma glioblastoma hepatitis C high grade glioma ovarian cancer ovarian carcinoma
377	ARF GTPase 3	ARF3	Homo sapiens (human)
374	amphiregulin	AREG	Homo sapiens (human)
372	archain 1	ARCN1	Homo sapiens (human)
368	ATP binding cassette subfamily C member 6	ABCC6	Homo sapiens (human)
367	androgen receptor	AR	Homo sapiens (human)
362	aquaporin 5	AQP5	Homo sapiens (human)
361	aquaporin 4	AQP4	Homo sapiens (human)
360	aquaporin 3 (Gill blood group)	AQP3	Homo sapiens (human)
359	aquaporin 2	AQP2	Homo sapiens (human)
358	aquaporin 1 (Colton blood group)	AQP1	Homo sapiens (human)
356	Fas ligand	FASLG	Homo sapiens (human)
355	Fas cell surface death receptor	FAS	Homo sapiens (human)
354	kallikrein related peptidase 3	KLK3	Homo sapiens (human)
353	adenine phosphoribosyltransferase	APRT	Homo sapiens (human)	Albright's hereditary osteodystrophy 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 Barrett's esophagus Becker muscular dystrophy Bloom syndrome Brucella melitensis brucellosis Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome Carney complex Danon disease Duchenne muscular dystrophy Gerstmann-Straussler-Scheinker syndrome Gorham's disease Graves' disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Japanese encephalitis Langerhans-cell histiocytosis Lesch-Nyhan syndrome Lown-Ganong-Levine syndrome Marfan syndrome McCune Albright syndrome Meckel syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Peutz-Jeghers syndrome Pick's disease Q fever Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia Werdnig-Hoffmann disease Werner syndrome Wolff-Parkinson-White syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 acquired hyperkeratosis acrodermatitis acrodysostosis acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction acute promyelocytic leukemia adenine phosphoribosyltransferase deficiency adenocarcinoma adenoma adenosarcoma adrenal gland cancer adrenal gland hyperfunction adrenoleukodystrophy adult T-cell leukemia/lymphoma adult acute lymphocytic leukemia adult fibrosarcoma adult hepatocellular carcinoma adult medulloblastoma alcohol dependence alcohol use disorder allergic asthma amyloidosis amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anaplastic astrocytoma anterior horn cell disease arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis atrichia with papular lesions atrioventricular block attention deficit hyperactivity disorder autistic disorder autoimmune polyendocrine syndrome autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal dominant polycystic kidney disease autosomal recessive distal hereditary motor neuronopathy 1 autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bacterial infectious disease bacterial sepsis benign mesothelioma bile duct adenocarcinoma bile duct cancer bile duct carcinoma bladder carcinoma bone osteosarcoma brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ cherubism childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood hepatocellular carcinoma childhood leukemia childhood medulloblastoma childhood optic nerve glioma childhood osteosarcoma childhood spinal muscular atrophy cholangiocarcinoma cholera chondrosarcoma choriocarcinoma chromophobe renal cell carcinoma chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation congenital muscular dystrophy congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma cystic fibrosis cystinosis cystinuria dengue disease depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis diarrhea diffuse large B-cell lymphoma disease of metabolism distal arthrogryposis distal myopathy duodenum cancer dysentery dysthymic disorder embryoma encephalitis encephalomyelitis endocarditis endocrine exophthalmos endometrial cancer endometrial carcinoma endomyocardial fibrosis epilepsy episodic kinesigenic dyskinesia 1 esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension exostosis facioscapulohumeral muscular dystrophy familial hyperlipidemia familial hypertrophic cardiomyopathy familial retinoblastoma fibrillary astrocytoma fibrodysplasia ossificans progressiva fibrolamellar carcinoma fibromyalgia fibrosarcoma fibrous dysplasia follicular adenoma fragile X syndrome galactosemia gallbladder cancer gallbladder carcinoma gemistocytic astrocytoma giant cell glioblastoma glaucoma glioblastoma gliosarcoma glomerulonephritis glucose intolerance glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease IV glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease V glycogen storage disease VI glycogen storage disease VII glycogen storage disease glycoproteinosis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart cancer heart disease hepatitis B hepatitis C hepatitis hepatoblastoma hepatocellular carcinoma hereditary breast ovarian cancer syndrome high grade glioma hyperglycemia hypertension hyperthyroidism hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy hypoglycemia hypoparathyroidism hypothalamic disease idiopathic interstitial pneumonia immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome impulse control disorder influenza intermittent explosive disorder interstitial nephritis intestinal infectious disease intrahepatic cholangiocarcinoma intrinsic asthma irritant dermatitis juvenile pilocytic astrocytoma juvenile spinal muscular atrophy keratosis follicularis kidney cancer kidney disease kidney failure kleptomania large intestine cancer lateral sclerosis leishmaniasis leukemia leukoencephalopathy with vanishing white matter limb-girdle muscular dystrophy lipoatrophic diabetes mellitus lipodystrophy liver cancer liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder malignant astrocytoma malignant mesothelioma malignant pleural mesothelioma maturity-onset diabetes of the young measles medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma meningitis methemoglobinemia microcystic adenoma microphthalmia mitochondrial metabolism disease mitochondrial myopathy mixed glioma mongolian spot motor neuron disease mucolipidosis II alpha/beta mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis VI mucopolysaccharidosis multiple acyl-CoA dehydrogenase deficiency multiple endocrine neoplasia type 1 multiple myeloma multiple sclerosis muscular dystrophy myasthenia gravis myelitis myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myositis ossificans myositis nasopharynx carcinoma nephritis nephroblastoma nephrolithiasis nephrosis neuroblastoma neuroendocrine carcinoma neuroendocrine tumor neurofibromatosis 1 neurofibromatosis neuromuscular disease neuropathy neurotic disorder non-Hodgkin lymphoma nonpapillary renal cell carcinoma nutmeg liver obesity obsolete Cushing's syndrome obsolete Matthew-Wood syndrome obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oculopharyngeal muscular dystrophy optic nerve glioma osteoarthritis osteoblastoma osteomalacia osteosarcoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma parapsoriasis parathyroid gland disease periodontitis peripheral nervous system disease pheochromocytoma pilocytic astrocytoma placenta cancer pneumonia polycystic kidney disease 1 polycystic ovary syndrome polyneuropathy postinflammatory pulmonary fibrosis prediabetes syndrome primary hyperaldosteronism primary hyperoxaluria primary hyperparathyroidism primary immunodeficiency disease primary pigmented nodular adrenocortical disease primary pulmonary hypertension progeria progressive muscular atrophy prostate adenocarcinoma prostate cancer prostate carcinoma protoplasmic astrocytoma pseudohypoparathyroidism pseudopseudohypoparathyroidism pseudoxanthoma elasticum psoriasis psoriatic arthritis pulmonary fibrosis purine-pyrimidine metabolic disorder pustulosis of palm and sole pyelitis pyelonephritis pyoureter radiculopathy renal carcinoma renal cell carcinoma reticulosarcoma retinoblastoma rheumatoid arthritis rickets rippling muscle disease 2 sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia sick sinus syndrome silent myocardial infarction situs inversus skin melanoma skin squamous cell carcinoma small intestine cancer steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma sulfhemoglobinemia systemic lupus erythematosus thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma thyrotoxicosis trilateral retinoblastoma trypanosomiasis tuberculosis tuberous sclerosis 1 tuberous sclerosis 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 typhus uremia uric acid nephrolithiasis urinary bladder cancer urinary tract obstruction uterine corpus cancer viral infectious disease visceral leishmaniasis von Hippel-Lindau disease yellow fever
351	amyloid beta precursor protein	APP	Homo sapiens (human)
350	apolipoprotein H	APOH	Homo sapiens (human)
348	apolipoprotein E	APOE	Homo sapiens (human)
347	apolipoprotein D	APOD	Homo sapiens (human)	Alzheimer's disease gestational diabetes obesity status epilepticus type 2 diabetes mellitus vasculogenic impotence
346	apolipoprotein C4	APOC4	Homo sapiens (human)
345	apolipoprotein C3	APOC3	Homo sapiens (human)

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