GlyCosmos Portal

Table Filtering

Gene ID

Gene Name

Gene Symbol

Organism

Taxonomy ID

Disease Ontology

Disease Ontology ID

Gene Ontology

Gene Ontology ID

Display
results per page.

Clear

Submissions

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

Search results for "carbohydrate metabolic process"

Displaying entries **251 - 275** of **78965** in total

« First

‹ Prev

…

7

8

9

10

11

12

13

14

15

…

Next ›

Last »
Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
9331	beta-1,4-galactosyltransferase 6	B4GALT6 Aliases: UDP-Gal:glucosylceramide beta-1,4-galactosyltransferase beta4GalT-VI	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer multiple sclerosis skin disease
9334	beta-1,4-galactosyltransferase 5	B4GALT5 Aliases: beta4-GalT IV beta4GalT-V	Homo sapiens (human)	cancer central nervous system cancer colorectal cancer colorectal carcinoma diabetes mellitus diabetic ketoacidosis embryoma gliosarcoma high grade glioma large intestine cancer mixed glioma multiple sclerosis obesity type 2 diabetes mellitus
9348	N-deacetylase and N-sulfotransferase 3	NDST3 Aliases: HSST3	Homo sapiens (human)	Balo concentric sclerosis adrenoleukodystrophy anxiety disorder autism spectrum disorder azoospermia central nervous system disease depressive disorder generalized anxiety disorder intellectual disability major depressive disorder melancholic depression narcolepsy neurotic disorder obsolete melancholia schizophrenia
9365	klotho	KL Aliases: KLA alpha-klotho	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 Burkitt lymphoma Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Duchenne muscular dystrophy Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IgA glomerulonephritis Kummell's disease 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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Prader-Willi syndrome Prinzmetal angina Reye syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Smith-McCort dysplasia Werner syndrome X-linked Aarskog syndrome X-linked dominant hypophosphatemic rickets Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acromegaly actinic keratosis acute myocardial infarction acute pancreatitis adenocarcinoma adenoma adult respiratory distress syndrome alcohol dependence alcohol use disorder alternating hemiplegia of childhood amnestic disorder amyotrophic lateral sclerosis androgen insensitivity syndrome anemia aortic valve disease 1 aortic valve disease aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation autonomic neuropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant polycystic kidney disease autosomal recessive Robinow syndrome bacterial infectious disease bacterial sepsis beta thalassemia bicuspid aortic valve disease bipolar disorder bladder carcinoma bone disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer cardiomyopathy cardiovascular system disease carotid artery disease carotid artery thrombosis carotid stenosis cartilage disease central nervous system disease cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma chondrocalcinosis chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma chronic fatigue syndrome chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy congestive heart failure connective tissue disease coronary artery disease coronary stenosis coronary thrombosis cribriform carcinoma dedifferentiated liposarcoma dementia demyelinating disease depressive disorder diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism dysthymic disorder embryoma encephalitis encephalomyelitis end stage renal disease endomyocardial fibrosis enthesopathy epilepsy essential hypertension exostosis familial adenomatous polyposis familial hyperlipidemia familial nephrotic syndrome follicular adenoma fundus albipunctatus gastroenteritis giant cell glioblastoma glioblastoma glomerulonephritis granular cell carcinoma growth hormone secreting pituitary adenoma head and neck squamous cell carcinoma heart disease hematologic cancer hepatocellular carcinoma high grade glioma hypercalcemia hyperglycemia hyperinsulinism hyperparathyroidism hyperphosphatemia hyperphosphatemic familial tumoral calcinosis hyperpituitarism hypertension hypertrophic cardiomyopathy hypoglycemia hypophosphatemia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis infertility insulinoma intellectual disability intracranial embolism invasive ductal carcinoma kidney cancer kidney disease kidney failure kidney hypertrophy kwashiorkor large intestine cancer late onset Parkinson's disease learning disability lipoid nephrosis liposarcoma liver cancer liver cirrhosis localized scleroderma lung benign neoplasm lung cancer lung carcinoma lung large cell carcinoma lung non-small cell carcinoma lung small cell carcinoma lung squamous cell carcinoma macrocytic anemia major depressive disorder marasmus melancholic depression melanoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic adenoma microphthalmia middle cerebral artery infarction monoclonal gammopathy of uncertain significance mood disorder multiple myeloma multiple sclerosis muscular dystrophy musculoskeletal system disease myelitis myocardial infarction myositis nephritis nephrocalcinosis nephrolithiasis nephrosis nephrotic syndrome nervous system disease neurodegenerative disease neurotic disorder newborn respiratory distress syndrome nonpapillary renal cell carcinoma nutmeg liver nutrition disease obesity obsolete Matthew-Wood syndrome obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma obstructive sleep apnea osteitis fibrosa osteoarthritis osteomalacia osteonecrosis osteoporosis ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis papillary adenoma papillary renal cell carcinoma parathyroid adenoma parathyroid carcinoma parathyroid gland disease periarthritis phosphorus metabolism disease placental insufficiency pleomorphic liposarcoma polycystic kidney disease 1 porphyria cutanea tarda postinflammatory pulmonary fibrosis premature menopause priapism primary hyperparathyroidism primary ovarian insufficiency primary pulmonary hypertension progeria progressive muscular atrophy prostate cancer prostate carcinoma protein-energy malnutrition pulmonary emphysema pulmonary fibrosis pulmonary large cell neuroendocrine carcinoma pyoureter reflex sympathetic dystrophy relapsing-remitting multiple sclerosis renal carcinoma renal cell carcinoma renal osteodystrophy retinal disease retinitis pigmentosa 1 retinitis pigmentosa retinitis retrograde amnesia rheumatoid arthritis rickets sarcomatoid renal cell carcinoma schizophrenia scleroderma seborrheic keratosis secondary hyperparathyroidism sickle cell anemia silent myocardial infarction skin disease skin melanoma spondyloarthropathy spondylosis squamous cell carcinoma systemic scleroderma tendinitis thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland follicular carcinoma tongue squamous cell carcinoma 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 uremia ureteral obstruction uric acid nephrolithiasis urinary bladder cancer vascular dementia vascular disease
9370	adiponectin, C1Q and collagen domain containing	ADIPOQ	Homo sapiens (human)	Alzheimer's disease Behcet's disease Crohn's disease Graves' disease Kawasaki disease Mycobacterium avium complex disease Rett syndrome amyloidosis ankylosing spondylitis atherosclerosis autoimmune hepatitis biliary atresia bipolar disorder brain infarction breast cancer cardiomyopathy cardiovascular system disease chronic obstructive pulmonary disease colitis congestive heart failure coronary aneurysm coronary artery disease dementia diabetic retinopathy diffuse scleroderma end stage renal disease familial hyperlipidemia familial mediterranean fever gestational diabetes graft-versus-host disease hepatocellular carcinoma hyperinsulinism hyperthyroidism inflammatory bowel disease liver cirrhosis metabolic dysfunction-associated steatotic liver disease multiple sclerosis myocardial infarction obesity peripheral artery disease polycystic ovary syndrome primary open angle glaucoma proliferative diabetic retinopathy prostate adenocarcinoma pulmonary tuberculosis rheumatoid arthritis sleep apnea steatotic liver disease tongue squamous cell carcinoma type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis vascular disease
9435	carbohydrate sulfotransferase 2	CHST2 Aliases: C6ST	Homo sapiens (human)	amyotrophic lateral sclerosis bone osteosarcoma cancer extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue gastric lymphoma inflammatory bowel disease 1 inflammatory bowel disease osteosarcoma progressive muscular atrophy ulcerative colitis
9446	glutathione S-transferase omega 1	GSTO1	Homo sapiens (human)	Alzheimer's disease Parkinson's disease alcohol use disorder
9469	carbohydrate sulfotransferase 3	CHST3 Aliases: C6ST C6ST1 chondroitin 6 sulfotransferase 1	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Bartter disease Conn's syndrome Cowden syndrome Desbuquois dysplasia Hailey-Hailey disease Laron syndrome Larsen syndrome Larsen-like syndrome B3GAT3 type Ollier disease Rothmund-Thomson syndrome SOST-related sclerosing bone dysplasia Schwartz-Jampel syndrome 1 Silverman-Handmaker type dyssegmental dysplasia Sjogren's syndrome Waterhouse-Friderichsen syndrome X-linked spondyloepiphyseal dysplasia tarda achondroplasia acute promyelocytic leukemia adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenocortical carcinoma adrenoleukodystrophy adult fibrosarcoma agnosia alcoholic hepatitis alcoholic liver cirrhosis amblyopia aortic valve disease 1 aortic valve disease 2 aortic valve insufficiency aortic valve stenosis apparent mineralocorticoid excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atopic dermatitis 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 atrophy of testis autoimmune hepatitis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa 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 bicuspid aortic valve disease blastomycosis breast cancer breast carcinoma buphthalmos cancer cardiomyopathy cardiovascular system disease choriocarcinoma cleft palate cleidocranial dysplasia clubfoot communicating hydrocephalus congenital adrenal hyperplasia coronary artery disease craniosynostosis cutis laxa cystadenoma dermatitis developmental coordination disorder diabetes mellitus diabetic ketoacidosis diastrophic dysplasia embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis endomyocardial fibrosis enterocele esotropia essential hypertension fibrosarcoma follicular adenoma heart disease hepatitis hereditary multiple exostoses humeroradial synostosis hydrocephalus hydrophthalmos hyperopia hypertension hypertrophic cardiomyopathy hypogonadotropic hypogonadism 23 with or without anosmia inclusion body myositis intrahepatic cholestasis isolated cleft palate juvenile glaucoma keratoconjunctivitis sicca leiomyoma liver cirrhosis lung small cell carcinoma mal de Meleda microcystic adenoma mitral valve insufficiency mitral valve prolapse mitral valve stenosis monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia myofibroma neurogenic arthropathy obesity obsolete type 1 diabetes mellitus 9 obstructive hydrocephalus osteochondrodysplasia osteoporosis ovarian cancer ovarian carcinoma ovarian hyperstimulation syndrome papillary adenoma paracoccidioidomycosis patent foramen ovale placenta cancer polycystic ovary syndrome postural orthostatic tachycardia syndrome primary hyperaldosteronism primary pulmonary hypertension progressive familial intrahepatic cholestasis progressive pseudorheumatoid arthropathy of childhood pulmonary valve stenosis radioulnar synostosis restrictive dermopathy rheumatoid arthritis schizophrenia scoliosis senile degeneration of brain sensorineural hearing loss spondyloepiphyseal dysplasia congenita spondyloepiphyseal dysplasia with congenital joint dislocations strabismic amblyopia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tricuspid valve insufficiency tricuspid valve stenosis 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 uterine corpus cancer uterine fibroid varicose veins ventricular septal defect
9486	carbohydrate sulfotransferase 10	CHST10 Aliases: HNK-1ST	Homo sapiens (human)	Japanese encephalitis dengue disease schizophrenia viral infectious disease yellow fever
9526	mannose-P-dolichol utilization defect 1	MPDU1 Aliases: CDGIf Lec35 PQLC5 SL15 SLC66A5	Homo sapiens (human)	IgA glomerulonephritis acquired hyperkeratosis autosomal recessive congenital ichthyosis 1 blindness cancer cerebral degeneration congenital disorder of glycosylation Id congenital disorder of glycosylation If congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation congenital hypothyroidism congenital nystagmus craniosynostosis cystinuria dissociated nystagmus galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hypertropia hypothyroidism ichthyosis keratosis follicularis mechanical strabismus microcephaly mongolian spot myxedema obsolete congenital ichthyosiform erythroderma ophthalmoplegia optic atrophy pathologic nystagmus pseudoxanthoma elasticum spontaneous ocular nystagmus strabismus
9563	hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase	H6PD Aliases: 6-phosphogluconolactonase GDH/6PGL endoplasmic bifunctional protein H6PDH	Homo sapiens (human)	Alzheimer's disease B-cell lymphoma Laron syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acne aromatase excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis beta thalassemia breast cancer breast carcinoma cancer cardiovascular system disease cholangiocarcinoma colorectal cancer cone-rod dystrophy 2 cone-rod dystrophy coronary artery disease cortisone reductase deficiency 1 cortisone reductase deficiency dementia diabetes insipidus diabetes mellitus diabetic ketoacidosis diarrhea gallbladder disease giardiasis heart disease hemolytic anemia hyperandrogenism hyperinsulinism hypertrichosis hypoglycemia infertility intrahepatic cholangiocarcinoma large intestine cancer leishmaniasis liver disease luminal breast carcinoma A malaria multiple sclerosis neurohypophyseal diabetes insipidus obesity obsolete ymphosarcoma placental insufficiency polycystic ovary syndrome primary hyperoxaluria steatotic liver disease thalassemia type 2 diabetes mellitus visceral leishmaniasis
9572	nuclear receptor subfamily 1 group D member 1	NR1D1	Homo sapiens (human)	alcoholic liver cirrhosis brain small vessel disease hyperthyroidism hypothyroidism portal hypertension type 2 diabetes mellitus
9653	heparan sulfate 2-O-sulfotransferase 1	HS2ST1 Aliases: KIAA0448	Homo sapiens (human)	benign mastocytoma extracutaneous mastocytoma hypereosinophilic syndrome indolent systemic mastocytosis mast cell neoplasm mastocytosis melanoma skin melanoma
9695	ER degradation enhancing alpha-mannosidase like protein 1	EDEM1 Aliases: EDEM KIAA0212	Homo sapiens (human)	cystic fibrosis depressive disorder hepatitis C major depressive disorder melancholic depression melanoma neurotic disorder obsolete melancholia skin melanoma
9746	calsyntenin 3	CLSTN3	Homo sapiens (human)
9852	EPM2A interacting protein 1	EPM2AIP1	Homo sapiens (human)
9942	xylulokinase	XYLB	Homo sapiens (human)	cerebral infarction cerebrovascular disease
9962	solute carrier family 23 member 2	SLC23A2	Homo sapiens (human)
9963	solute carrier family 23 member 1	SLC23A1	Homo sapiens (human)
10007	glucosamine-6-phosphate deaminase 1	GNPDA1 Aliases: GNPDA GPI HLN KIAA0060 glucosamine-6-phosphate deaminase oscillin	Homo sapiens (human)
10020	glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase	GNE Aliases: Uae1 bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase	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 Bell's palsy GNE myopathy Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Paget's disease of bone Pick's disease Reye syndrome X-linked myopathy with excessive autophagy Zika fever amnestic disorder attention deficit hyperactivity disorder 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 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 cancer cardiomyopathy cerebral degeneration cholangiocarcinoma cholecystolithiasis choledocholithiasis cholelithiasis chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma congenital central hypoventilation syndrome congenital hypothyroidism dementia distal myopathy endomyocardial fibrosis epilepsy esophagitis facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis frontotemporal dementia gastroesophageal reflux disease hypertrophic cardiomyopathy hypothyroidism inclusion body myopathy with Paget disease of bone and frontotemporal dementia inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 inclusion body myositis inguinal hernia intrahepatic cholangiocarcinoma isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy mixed sleep apnea mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis muscular dystrophy myopathy myositis myxedema neuromuscular disease nonpapillary renal cell carcinoma 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 obstructive sleep apnea oculopharyngeal muscular dystrophy pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma peptic esophagitis renal carcinoma renal cell carcinoma retrograde amnesia sarcomatoid renal cell carcinoma scoliosis sialuria sleep apnea thrombocytopenia tibial muscular dystrophy visual epilepsy
10090	uronyl 2-sulfotransferase	UST Aliases: 2OST	Homo sapiens (human)	Crohn's colitis Crohn's disease ankylosing spondylitis arthritis arthropathy atrial fibrillation attention deficit hyperactivity disorder cancer endometriosis of ovary endometriosis of uterus endometriosis inflammatory bowel disease 1 inflammatory bowel disease osteoarthritis ulcerative colitis
10164	carbohydrate sulfotransferase 4	CHST4 Aliases: HEC-GLCNAC-6-ST LSST	Homo sapiens (human)	arthritis arthropathy cancer colitis colon cancer colon carcinoma colon mucinous adenocarcinoma colonic benign neoplasm colorectal cancer gastroenteritis ileitis ileocolitis large intestine cancer osteoarthritis
10165	solute carrier family 25 member 13	SLC25A13	Homo sapiens (human)	adult-onset type II citrullinemia citrullinemia common bile duct disease intrahepatic cholestasis neonatal-onset type II citrullinemia
10314	LanC like glutathione S-transferase 1	LANCL1	Homo sapiens (human)

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

Guidelines

International Collaboration

Acknowledgements