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	July 8, 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 **326 - 350** of **1582** in total

« First

‹ Prev

…

10

11

12

13

14

15

16

17

18

…

Next ›

Last »
Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
23305	acyl-CoA synthetase long chain family member 6	ACSL6 Aliases: ACS2 KIAA0837 LACS2 LACS5	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 Pick's disease Reye syndrome acute chest syndrome acute myeloid leukemia acute myocardial infarction amphetamine abuse androgen insensitivity syndrome arthritis arthropathy cancer cerebral degeneration congestive heart failure coronary thrombosis disease of mental health essential thrombocythemia hematologic cancer leukemia male infertility myelodysplastic syndrome myocardial infarction osteoarthritis plasmacytoma polycythemia vera polycythemia premature menopause primary ovarian insufficiency psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder silent myocardial infarction
116285	acyl-CoA synthetase medium chain family member 1	ACSM1 Aliases: MACS1	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 carcinoma cerebral palsy depressive disorder essential hypertension hemiplegia hypertension idiopathic scoliosis lung benign neoplasm lung carcinoma major depressive disorder melancholic depression neurotic disorder obsolete melancholia sarcomatoid carcinoma schizophrenia spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy
123876	acyl-CoA synthetase medium chain family member 2A	ACSM2A Aliases: A-923A4.1 MGC150530	Homo sapiens (human)	cerebral palsy hemiplegia spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy
348158	acyl-CoA synthetase medium chain family member 2B	ACSM2B Aliases: HXMA HYST1046 xenobiotic/medium chain fatty acid:CoA ligase	Homo sapiens (human)
6296	acyl-CoA synthetase medium chain family member 3	ACSM3 Aliases: SA	Homo sapiens (human)	IgA glomerulonephritis Kallmann syndrome Marfan syndrome Sheehan syndrome abdominal obesity-metabolic syndrome 1 anemia autism spectrum disorder autistic disorder bacterial sepsis brain cancer brain stem infarction breast cancer breast carcinoma cancer cardiovascular system disease cataract cerebral artery occlusion cerebral infarction cerebrovascular disease chronic kidney disease communicating hydrocephalus diabetes mellitus diabetic ketoacidosis embryoma epilepsy essential hypertension essential thrombocythemia generalized atherosclerosis heart disease hemosiderosis hepatocellular carcinoma hereditary coproporphyria hydrocephalus hyperglycemia hypertension hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism idiopathic scoliosis intracranial aneurysm intracranial vasospasm isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency liver cancer liver carcinoma macrocytic anemia obesity obstructive hydrocephalus ocular hypertension oculomotor nerve paralysis panhypopituitarism partial third-nerve palsy post-traumatic stress disorder prostate cancer prostate carcinoma senile degeneration of brain sensorineural hearing loss situs inversus tetralogy of Fallot thrombophilia thymus gland disease total third-nerve palsy transient cerebral ischemia tuberous sclerosis ulcerative colitis visual epilepsy
341392	acyl-CoA synthetase medium chain family member 4	ACSM4 Aliases: similar to olfactory specific medium-chain acyl CoA synthetase	Homo sapiens (human)
54988	acyl-CoA synthetase medium chain family member 5	ACSM5 Aliases: FLJ20581	Homo sapiens (human)
142827	acyl-CoA synthetase medium chain family member 6	ACSM6 Aliases: bA310E22.3	Homo sapiens (human)
84532	acyl-CoA synthetase short chain family member 1	ACSS1 Aliases: AceCS2L MGC33843 dJ568C11.3	Homo sapiens (human)	acute myocardial infarction bladder carcinoma cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary thrombosis embryoma lung cancer lung non-small cell carcinoma myocardial infarction papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction urinary bladder cancer
55902	acyl-CoA synthetase short chain family member 2	ACSS2 Aliases: ACS ACSA AceCS dJ1161H23.1	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 Crohn's colitis Crohn's disease Ewing sarcoma Klippel-Feil syndrome Marfan syndrome McCune Albright syndrome Pick's disease Reye syndrome Stevens-Johnson syndrome abdominal aortic aneurysm acquired immunodeficiency syndrome acute chest syndrome acute lymphoblastic leukemia acute myocardial infarction adult acute lymphocytic leukemia alcohol dependence alcohol use disorder aortic valve insufficiency appendicitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthropathy atherosclerosis atrial fibrillation bacterial sepsis bladder carcinoma breast cancer breast carcinoma cancer cardiac arrest cardiovascular system disease central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia cholecystolithiasis choledocholithiasis cholelithiasis chromophobe renal cell carcinoma chronic kidney disease chronic obstructive pulmonary disease clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital diaphragmatic hernia congestive heart failure coronary aneurysm coronary artery disease coronary thrombosis decubitus ulcer depressive disorder diabetes insipidus diabetes mellitus diabetic ketoacidosis disease of mental health distal arthrogryposis dysthymic disorder embryoma endometrial cancer endometrial carcinoma epithelioid sarcoma erythema multiforme esophageal cancer esophageal carcinoma esophageal disease esophagus squamous cell carcinoma essential hypertension familial adenomatous polyposis familial hypercholesterolemia gastroschisis giant cell glioblastoma glioblastoma gliosarcoma head and neck cancer heart disease hepatocellular carcinoma hiatus hernia high grade glioma human immunodeficiency virus infectious disease hypertension hypoplastic left heart syndrome impotence inflammatory bowel disease 1 inflammatory bowel disease insulinoma islet cell tumor kidney failure large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer leishmaniasis liver cancer liver carcinoma lung cancer lung non-small cell carcinoma lymphangioleiomyomatosis major depressive disorder melancholic depression mixed glioma morbid obesity myocardial infarction neuroendocrine carcinoma neuroendocrine tumor neurohypophyseal diabetes insipidus neurotic disorder nodular prostate nonpapillary renal cell carcinoma nutmeg liver obesity obsolete melancholia obstructive sleep apnea omphalocele orofacial cleft pancreatic adenocarcinoma pancreatic cancer papillary renal cell carcinoma peripheral artery disease pneumonia premature ejaculation primary hypertrophic osteoarthropathy prostate cancer prostate carcinoma prostatic adenoma psychologic dyspareunia psychotic disorder rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma retroperitoneal sarcoma sarcomatoid renal cell carcinoma septic arthritis silent myocardial infarction situs inversus spinal cancer spindle cell sarcoma spondylolisthesis steatotic liver disease stomach cancer stomach carcinoma stomach disease subacute delirium substance abuse substance-related disorder synovitis tenosynovitis thrombophilia thrombotic thrombocytopenic purpura tuberous sclerosis type 2 diabetes mellitus ulcerative colitis umbilical hernia uremia urinary bladder cancer urinary system benign neoplasm urinary system cancer uterine corpus cancer visceral leishmaniasis
79611	acyl-CoA synthetase short chain family member 3	ACSS3 Aliases: FLJ21963	Homo sapiens (human)	cancer embryoma stomach cancer stomach carcinoma
641371	acyl-CoA thioesterase 1	ACOT1 Aliases: ACH2 CTE-1 LACH2	Homo sapiens (human)	gastric adenocarcinoma hepatocellular carcinoma liver cancer
134526	acyl-CoA thioesterase 12	ACOT12 Aliases: Cach STARD15 StAR-related lipid transfer (START) domain containing 15 THEAL	Homo sapiens (human)	hepatocellular carcinoma leukodystrophy leukoencephalopathy with vanishing white matter liver cancer
10965	acyl-CoA thioesterase 2	ACOT2 Aliases: Mte1 ZAP128 mitochondrial acyl-CoA thioesterase 1	Homo sapiens (human)	coronary artery disease diabetes mellitus type 2 diabetes mellitus
122970	acyl-CoA thioesterase 4	ACOT4 Aliases: FLJ31235 PTE-Ib PTE2B	Homo sapiens (human)	cerebral infarction cerebrovascular disease
11332	acyl-CoA thioesterase 7	ACOT7 Aliases: ACH1 ACT BACH CTE-II LACH1 Long chain acyl-CoA thioester hydrolase MGC1126 brain acyl CoA hydrolase hBACH	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 Clouston syndrome Duchenne muscular dystrophy Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Plasmodium falciparum malaria Plasmodium vivax malaria Reye syndrome acute monocytic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenocortical carcinoma allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation bacterial infectious disease beta thalassemia blood coagulation disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral degeneration cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma chronic obstructive pulmonary disease clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer complex partial epilepsy congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma dementia depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea disease of mental health distal arthrogryposis dysentery dysthymic disorder eating disorder embryoma epilepsy esophagus squamous cell carcinoma female stress incontinence gallbladder disease gestational diabetes gestational trophoblastic neoplasm giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance granular cell carcinoma head and neck squamous cell carcinoma hepatitis A hepatitis hepatocellular carcinoma high grade glioma hypereosinophilic syndrome inclusion body myositis infertility intrinsic asthma kwashiorkor large intestine cancer leprosy liver cancer liver carcinoma liver disease lung benign neoplasm lung cancer lung carcinoma major depressive disorder malaria marasmus melancholic depression mixed glioma multiple sclerosis muscular dystrophy myocardial infarction neuroendocrine carcinoma neuroendocrine tumor neuropathy neurotic disorder nonpapillary renal cell carcinoma nutrition disease obsolete inherited blood coagulation disease obsolete melancholia obsolete type 1 diabetes mellitus 9 obstructive lung disease osteomyelitis ovarian cancer ovarian carcinoma papillary renal cell carcinoma peripheral nervous system disease peroxisome biogenesis disorder 7A pertussis polyneuropathy postpartum depression pre-eclampsia prediabetes syndrome primary open angle glaucoma primary ovarian insufficiency primary pulmonary hypertension progressive pseudorheumatoid arthropathy of childhood prostate cancer prostate carcinoma protein-energy malnutrition psychotic disorder pulmonary tuberculosis renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder scleroderma sick sinus syndrome silent myocardial infarction spermatic cord torsion systemic scleroderma temporal lobe epilepsy thalassemia tuberculosis tuberculous pneumothorax 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 urethral intrinsic sphincter deficiency viral infectious disease visual epilepsy
10005	acyl-CoA thioesterase 8	ACOT8 Aliases: NAP1 Nef (lentivirus myristoylated factor) associated protein 1 PTE-2 choloyl-CoA hydrolase hACTE-III hTE	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 Pick's disease Reye syndrome Thiel-Behnke corneal dystrophy acquired immunodeficiency syndrome bacterial sepsis cancer cerebral degeneration diabetes insipidus diarrhea embryoma hepatocellular carcinoma human immunodeficiency virus infectious disease hypophosphatemia liver cancer low tension glaucoma lung cancer lung non-small cell carcinoma neurohypophyseal diabetes insipidus parapsoriasis psoriasis pustulosis of palm and sole
55750	acylglycerol kinase	AGK Aliases: FLJ10842	Homo sapiens (human)	3-methylglutaconic aciduria Chanarin-Dorfman syndrome Sengers syndrome agnosia 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 breast cancer breast carcinoma cancer cardiomyopathy cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract central nervous system cancer cervical squamous cell carcinoma cervix uteri carcinoma in situ congenital muscular dystrophy congenital nystagmus corneal dystrophy developmental coordination disorder dissociated nystagmus distal myopathy embryoma endomyocardial fibrosis esophagus squamous cell carcinoma facioscapulohumeral muscular dystrophy familial hypertrophic cardiomyopathy familial periodic paralysis glaucoma gliosarcoma high grade glioma hypertrophic cardiomyopathy hypertropia lactic acidosis limb-girdle muscular dystrophy mechanical strabismus mitochondrial DNA depletion syndrome 12b mitochondrial metabolism disease mitochondrial myopathy mixed glioma muscular dystrophy myopathy myopia nasopharynx 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 oculopharyngeal muscular dystrophy ophthalmoplegia papillary adenocarcinoma papillary renal cell carcinoma pathologic nystagmus prostate cancer prostate carcinoma spontaneous ocular nystagmus squamous cell carcinoma strabismus thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma trichohepatoenteric syndrome 1
97	acylphosphatase 1	ACYP1	Homo sapiens (human)
98	acylphosphatase 2	ACYP2	Homo sapiens (human)	IgA glomerulonephritis bone osteosarcoma breast cancer bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma embryoma gastrointestinal system cancer gliosarcoma hepatocellular carcinoma high grade glioma kidney cancer large intestine cancer laryngeal squamous cell carcinoma liver cancer lung benign neoplasm lung cancer lung carcinoma microphthalmia mixed glioma obsolete Matthew-Wood syndrome osteomyelitis osteosarcoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma stomach cancer stomach carcinoma
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
55811	adenylate cyclase 10	ADCY10	Homo sapiens (human)
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
155	adrenoceptor beta 3	ADRB3	Homo sapiens (human)	Alzheimer's disease colitis congestive heart failure coronary artery disease cystic fibrosis diabetic retinopathy dilated cardiomyopathy 1H endometrial cancer gout hypertension metabolic dysfunction-associated steatotic liver disease obesity polycystic ovary syndrome rheumatoid arthritis type 2 diabetes mellitus
176	aggrecan	ACAN Aliases: CSPGCP aggrecan proteoglycan	Homo sapiens (human)	Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome Dowling-Degos disease Ehlers-Danlos syndrome Laron syndrome Lyme disease Marfan syndrome SADDAN Silverman-Handmaker type dyssegmental dysplasia Werner syndrome X-linked spondyloepiphyseal dysplasia tarda achondroplasia actinic keratosis amyloidosis anthracosilicosis aortic valve disease 1 aortic valve disease 2 aortic valve disease aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis atherosclerosis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome 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 bagassosis bicuspid aortic valve disease bone disease cancer cardiovascular system disease carpal tunnel syndrome cartilage disease cerebral infarction cerebrovascular disease cherubism chondroblastoma chondromalacia chondrosarcoma chordoma chorioamnionitis chronic interstitial cystitis ciliary body disease colon cancer colonic benign neoplasm colorectal cancer congestive heart failure connective tissue disease coronary artery disease degenerative disc disease dental fluorosis developmental and epileptic encephalopathy 39 diabetic ketoacidosis distal myopathy enterocele epithelioid sarcoma exostosis facioscapulohumeral muscular dystrophy 1 facioscapulohumeral muscular dystrophy heart disease hepatocellular carcinoma hereditary multiple exostoses hypochondroplasia hypogonadism hypogonadotropic hypogonadism 7 with or without anosmia immune system disease infantile myofibromatosis interstitial cystitis iris disease juvenile rheumatoid arthritis large intestine cancer laryngeal carcinoma laryngeal disease larynx cancer limb-girdle muscular dystrophy lipoma liver cancer mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis multiple epiphyseal dysplasia multiple sclerosis multiple symmetric lipomatosis muscular dystrophy neurogenic arthropathy nicotine dependence obesity obsessive-compulsive disorder obsessive-compulsive personality disorder 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 type 1 diabetes mellitus 9 oculopharyngeal muscular dystrophy osteoarthritis osteochondritis dissecans osteochondrodysplasia osteogenesis imperfecta panuveitis periarthritis peroxisome biogenesis disorder 5A pleomorphic lipoma pneumoconiosis polycystic ovary syndrome progeria progressive pseudorheumatoid arthropathy of childhood prune belly syndrome pseudoachondroplasia reticulate acropigmentation of Kitamura rheumatoid arthritis sarcoma schizophrenia scoliosis septic arthritis siderosis situs inversus spindle cell sarcoma spondylitis spondyloarthropathy spondyloepiphyseal dysplasia Kimberley type spondyloepiphyseal dysplasia congenita spondylosis status epilepticus tendinitis tracheal disease tropical spastic paraparesis tuberous sclerosis 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 uveitis

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

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements