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

Displaying entries **676 - 700** of **1582** in total

« First

‹ Prev

…

24

25

26

27

28

29

30

31

32

…

Next ›

Last »
Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
55556	enolase superfamily member 1	ENOSF1 Aliases: FUCD HSRTSBETA L-fuconate dehydratase TYMSAS rTS	Homo sapiens (human)	Down syndrome Hailey-Hailey disease Holt-Oram syndrome Klippel-Trenaunay syndrome Marfan syndrome Plasmodium falciparum malaria Rothmund-Thomson syndrome Rubinstein-Taybi syndrome VACTERL association Werner syndrome adult lymphoma arachnoiditis 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 cancer central nervous system cancer central nervous system lymphoma cerebral malaria childhood leukemia childhood lymphoma colorectal cancer colorectal carcinoma congenital central hypoventilation syndrome cutaneous mastocytosis cutis laxa diffuse cutaneous mastocytosis embryoma endometrial cancer endometrial carcinoma exanthem gliosarcoma hepatitis B herpes zoster high grade glioma intellectual disability large intestine cancer learning disability leukemia lymphoma mal de Meleda malaria mastocytosis meningitis microphthalmia with limb anomalies mixed glioma mixed sleep apnea nail-patella syndrome obsolete ymphosarcoma obstructive sleep apnea ovarian cancer ovarian carcinoma poikiloderma with neutropenia progeria rabies restrictive dermopathy situs inversus sleep apnea split hand-foot malformation 1 with sensorineural hearing loss stomach cancer stomach carcinoma thrombocytopenia-absent radius syndrome tuberous sclerosis urticaria pigmentosa uterine corpus cancer
1632	enoyl-CoA delta isomerase 1	ECI1 Aliases: 3,2 trans-enoyl-CoA isomerase	Homo sapiens (human)	achalasia carcinoma congenital diaphragmatic hernia dilated cardiomyopathy 1A dilated cardiomyopathy esophagitis gastroesophageal reflux disease hiatus hernia megaesophagus peptic esophagitis
10455	enoyl-CoA delta isomerase 2	ECI2 Aliases: ACBD2 DRS1 HCA88 Hepatocellular carcinoma-associated antigen 88 acyl-Coenzyme A binding domain containing 2	Homo sapiens (human)	aplastic anemia paroxysmal nocturnal hemoglobinuria prostate cancer prostate carcinoma pure red-cell aplasia
1962	enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase	EHHADH	Homo sapiens (human)	D-bifunctional protein deficiency Fanconi renotubular syndrome 3 Fanconi syndrome Laron syndrome Zollinger-Ellison syndrome achondroplasia amyloidosis bipolar disorder cancer carnitine palmitoyltransferase II deficiency cystinosis cystinuria cytochrome-c oxidase deficiency disease familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatocellular carcinoma hyperinsulinemic hypoglycemia hyperinsulinism liver cancer liver disease mitochondrial trifunctional protein deficiency osteomalacia prostate cancer prostate carcinoma proteinuria rickets spondyloepimetaphyseal dysplasia, Sponastrime type substance abuse substance-related disorder tuberculosis
1892	enoyl-CoA hydratase, short chain 1	ECHS1 Aliases: SCEH short chain enoyl-CoA hydratase	Homo sapiens (human)	3-methylglutaconic aciduria Balo concentric sclerosis Hailey-Hailey disease Leigh disease Rothmund-Thomson syndrome adrenoleukodystrophy alcohol dependence alcohol use disorder anemia 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 breast cancer breast carcinoma cancer cardiomyopathy central nervous system disease childhood onset GLUT1 deficiency syndrome 2 chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma cone-rod dystrophy congenital nystagmus congenital ptosis cutis laxa disease of metabolism dissociated nystagmus dystonia embryoma endomyocardial fibrosis epilepsy familial hypertrophic cardiomyopathy focal hand dystonia fundus albipunctatus generalized dystonia giant cell glioblastoma glioblastoma hepatitis A hepatitis hepatocellular carcinoma high grade glioma hypertrichosis hypertrophic cardiomyopathy hypertropia inherited metabolic disorder lactic acidosis leukodystrophy lingual-facial-buccal dyskinesia liver cancer liver carcinoma macrocytic anemia mal de Meleda mechanical strabismus mitochondrial metabolism disease narcolepsy nervous system disease neuropathy nonpapillary renal cell carcinoma obesity ophthalmoplegia optic atrophy overnutrition papillary renal cell carcinoma pathologic nystagmus peripheral nervous system disease periventricular leukomalacia ptosis pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency renal carcinoma renal cell carcinoma restrictive dermopathy retinitis pigmentosa sarcomatoid renal cell carcinoma sensorineural hearing loss spontaneous ocular nystagmus stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability 94 ventricular septal defect visual epilepsy
1942	ephrin A1	EFNA1 Aliases: ECKLG EPH-related receptor tyrosine kinase ligand 1 GMAN LERK1 Tumor necrosis factor alpha-induced protein 4 gastric cancer metastasis associated long noncoding RNA	Homo sapiens (human)	acute myocardial infarction adenocarcinoma adenoma allergic asthma arteriovenous malformation asthma benign giant cell tumor bladder carcinoma bone osteosarcoma botryoid rhabdomyosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer childhood osteosarcoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon carcinoma colorectal cancer colorectal carcinoma coronary thrombosis cribriform carcinoma diabetic ketoacidosis distal arthrogryposis embryoma embryonal rhabdomyosarcoma esophagus squamous cell carcinoma gliosarcoma granular cell carcinoma hepatocellular carcinoma high grade glioma intestinal benign neoplasm intestinal cancer intrinsic asthma large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma malignant pleural mesothelioma melanoma mixed glioma myocardial infarction nonpapillary renal cell carcinoma obsolete type 1 diabetes mellitus 9 osteosarcoma ovarian cancer ovarian carcinoma papillary renal cell carcinoma pre-eclampsia primary pulmonary hypertension renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma squamous cell carcinoma stomach cancer stomach carcinoma tongue squamous cell carcinoma transitional 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 urinary bladder cancer
1943	ephrin A2	EFNA2 Aliases: ELF-1 EPH-related receptor tyrosine kinase ligand 6 LERK6	Homo sapiens (human)	acute myeloid leukemia breast cancer breast carcinoma cancer cervical adenocarcinoma cervical cancer cervix carcinoma chronic granulomatous disease embryoma endometrial cancer endometrial carcinoma familial retinoblastoma gastrointestinal system cancer giant cell glioblastoma glioblastoma high grade glioma lupus erythematosus nasopharynx carcinoma nodular prostate pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma prostatic adenoma retinoblastoma stomach cancer stomach carcinoma systemic lupus erythematosus trilateral retinoblastoma uterine corpus cancer
1946	ephrin A5	EFNA5 Aliases: AF1 EPH-related receptor tyrosine kinase ligand 7 LERK7	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 Ambras type hypertrichosis universalis congenita IGSF1 deficiency syndrome Norum disease Pick's disease Reye syndrome Tangier disease abdominal aortic aneurysm abetalipoproteinemia acquired immunodeficiency syndrome acute lymphoblastic leukemia acute myeloid leukemia adult medulloblastoma amyotrophic lateral sclerosis anencephaly arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness breast cancer breast carcinoma bulimia nervosa cancer cardiovascular system disease cataract cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease childhood medulloblastoma chondrosarcoma choreaacanthocytosis colitis conduct disorder congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 coronary artery disease cystic fibrosis diffuse large B-cell lymphoma embryoma enophthalmos familial hypobetalipoproteinemia 1 gastric ulcer gastroenteritis heart disease hemiplegia hepatocellular carcinoma human immunodeficiency virus infectious disease hypobetalipoproteinemia hypolipoproteinemia hypothyroidism ileitis ileocolitis infertility inflammatory bowel disease 1 inflammatory bowel disease liver cancer lymphoblastic lymphoma medulloblastoma medullomyoblastoma melanotic medulloblastoma myxedema nicotine dependence nutmeg liver obsessive-compulsive disorder obsolete exophthalmos orbital disease peripheral vascular disease progressive muscular atrophy prostate cancer prostate carcinoma schizophrenia sclerocornea senile cataract spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy synovitis systemic lupus erythematosus tenosynovitis thrombocytopenia ulcerative colitis
2053	epoxide hydrolase 2	EPHX2 Aliases: ABHD20 bifunctional epoxide hydrolase sEH soluble epoxide hydrolase	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 Crohn's colitis Crohn's disease IgA glomerulonephritis Langerhans-cell histiocytosis Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sertoli cell-only syndrome Y-linked spermatogenic failure 1 abdominal obesity-metabolic syndrome 1 acute chest syndrome acute kidney failure acute myocardial infarction adenocarcinoma adenoma adult respiratory distress syndrome anorexia nervosa arcus senilis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation autism spectrum disorder autistic disorder blindness brain stem infarction bronchus cancer bronchus carcinoma cancer cardiovascular system disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical squamous cell carcinoma chronic kidney disease chronic obstructive pulmonary disease complement deficiency complex partial epilepsy congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma dementia depressive disorder diabetes mellitus embryoma essential hypertension exudative vitreoretinopathy 1 exudative vitreoretinopathy eyelid disease familial hypercholesterolemia gastrointestinal stromal tumor glomerulonephritis granular cell carcinoma heart disease hyperglycemia hypertension hypertrophic cardiomyopathy inflammatory bowel disease 1 inflammatory bowel disease kidney disease lobular neoplasia lung benign neoplasm lung cancer lung carcinoma lupus erythematosus lupus nephritis lymphoma major depressive disorder melancholic depression middle cerebral artery infarction myocardial infarction nephritis newborn respiratory distress syndrome non-Hodgkin lymphoma nutmeg liver obsolete melancholia obsolete ymphosarcoma oligospermia pancreatic cancer pancreatic carcinoma pneumonia primary pulmonary hypertension prostate cancer prostate carcinoma pulmonary emphysema pulmonary hypertension reticulosarcoma retinopathy of prematurity sarcoidosis schizophrenia sick sinus syndrome silent myocardial infarction sudden infant death syndrome systemic lupus erythematosus temporal lobe epilepsy tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis uveoparotid fever xanthomatosis
55500	ethanolamine kinase 1	ETNK1 Aliases: EKI EKI1	Homo sapiens (human)	aggressive systemic mastocytosis atypical chronic myeloid leukemia, BCR-ABL1 negative cancer chronic monocytic leukemia chronic myeloid leukemia chronic myelomonocytic leukemia disseminated eosinophilic collagen disease epilepsy heart conduction disease hypereosinophilic syndrome indolent systemic mastocytosis juvenile myelomonocytic leukemia mastocytosis microcephaly myeloid leukemia obsolete subacute myeloid leukemia seminoma systemic mastocytosis testicular cancer testicular germ cell cancer testis seminoma
55224	ethanolamine kinase 2	ETNK2 Aliases: EKI2 FLJ10761	Homo sapiens (human)	epilepsy heart conduction disease microcephaly
64850	ethanolamine-phosphate phospho-lyase	ETNPPL	Homo sapiens (human)	bipolar disorder borderline personality disorder cancer hepatocellular carcinoma intermittent explosive disorder liver cancer schizophrenia steatotic liver disease
55862	ethylmalonyl-CoA decarboxylase 1	ECHDC1 Aliases: dJ351K20.2	Homo sapiens (human)	bladder carcinoma breast cancer breast carcinoma melanoma ovarian cancer ovarian carcinoma skin melanoma urinary bladder cancer
2131	exostosin glycosyltransferase 1	EXT1 Aliases: Glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N- acetylglucosaminyltransferase N-acetylglucosaminyl-proteoglycan 4-beta-glucuronosyltransferase ttv	Homo sapiens (human)	Alzheimer's disease Cenani-Lenz syndactyly syndrome Cornelia de Lange syndrome 4 Cornelia de Lange syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Laron syndrome Legg-Calve-Perthes disease Lennox-Gastaut syndrome Leri-Weill dyschondrosteosis Maffucci syndrome Ollier disease Pick's disease Reye syndrome Ritter's disease Werner syndrome achondroplasia acute lymphoblastic leukemia adenocarcinoma adenoma adult acute lymphocytic leukemia anaplastic astrocytoma antisocial personality disorder arthritis arthropathy autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma cancer cartilage disease central nervous system cancer cerebral degeneration cervix uteri carcinoma in situ cherubism childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood leukemia chondroblastoma chondroma chondrosarcoma cleidocranial dysplasia clubfoot conduct disorder connective tissue disease cranial nerve disease cranial nerve palsy cribriform carcinoma cryoglobulinemia diabetes mellitus disease of mental health embryoma endometrial cancer endometrial carcinoma epilepsy exostosis familial hypercholesterolemia familial nephrotic syndrome fibrillary astrocytoma fibromyalgia frontotemporal dementia gallbladder disease gemistocytic astrocytoma gliosarcoma granular cell carcinoma head and neck squamous cell carcinoma hepatitis A hepatitis B hepatitis C hepatitis E hepatitis hepatocellular carcinoma hereditary multiple exostoses high grade glioma humeroradial synostosis hydrocephalus hyperostosis hypogonadism hypogonadotropic hypogonadism 7 with or without anosmia immune system disease intellectual disability juvenile myoclonic epilepsy juvenile pilocytic astrocytoma learning disability leukemia lipoid nephrosis liver cancer liver disease lupus nephritis malignant astrocytoma membranous glomerulonephritis metachondromatosis microcephaly mixed glioma mucopolysaccharidosis III mucopolysaccharidosis type IIIA multiple myeloma myositis nephrotic syndrome osteoarthritis osteonecrosis osteopoikilosis osteoporosis osteosarcoma periarthritis personality disorder pilocytic astrocytoma progeria protoplasmic astrocytoma psychotic disorder radioulnar synostosis rectal benign neoplasm rectum adenocarcinoma rectum cancer rheumatoid arthritis schizophrenia scoliosis spinal cord disease subependymal giant cell astrocytoma tendinitis thrombophilia trichorhinophalangeal syndrome type II tubular adenocarcinoma type 2 diabetes mellitus urinary tract obstruction uterine corpus cancer vasculitis vesicoureteral reflux visual epilepsy
2132	exostosin glycosyltransferase 2	EXT2 Aliases: Glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N- acetylglucosaminyltransferase N-acetylglucosaminyl-proteoglycan 4-beta-glucuronosyltransferase SOTV	Homo sapiens (human)	Alzheimer's disease Cenani-Lenz syndactyly syndrome Dent disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Laron syndrome Leri-Weill dyschondrosteosis Maffucci syndrome Marfan syndrome Ollier disease Pick's disease Reye syndrome achondroplasia adenosarcoma agnosia anemia arthritis arthropathy autoimmune disease autoimmune lymphoproliferative syndrome bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma cancer cartilage disease cerebral degeneration cherubism chondrosarcoma cleidocranial dysplasia clubfoot congenital hypothyroidism congenital nystagmus connective tissue disease cranial nerve disease cranial nerve palsy craniosynostosis cryptorchidism developmental and epileptic encephalopathy 36 developmental coordination disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus epilepsy esophagitis essential hypertension exostosis familial hypercholesterolemia frontotemporal dementia gastroesophageal reflux disease hereditary multiple exostoses humeroradial synostosis hyperostosis hypertension hypertropia hypothyroidism immune system disease intellectual disability large intestine cancer learning disability lupus nephritis macrocytic anemia mechanical strabismus membranous glomerulonephritis metachondromatosis microcephaly mucopolysaccharidosis III mucopolysaccharidosis type IIIA myxedema nephroblastoma nonsyndromic congenital nail disorder 9 obsolete constipation ophthalmoplegia osteoarthritis osteonecrosis osteosarcoma parietal foramina pathologic nystagmus peptic esophagitis periarthritis radioulnar synostosis scoliosis situs inversus spontaneous ocular nystagmus stereotypic movement disorder strabismus tendinitis tuberous sclerosis type 2 diabetes mellitus ventricular septal defect visual epilepsy
2134	exostosin like glycosyltransferase 1	EXTL1 Aliases: EXTL MGC70794 alpha-N-acetylglucosaminyltransferase II exostosin-L glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N- acetylglucosaminyltransferase glucuronyl-N-acetylglucosaminylproteoglycan alpha-1,4-N- acetylglucosaminyltransferase	Homo sapiens (human)	cancer embryoma hereditary multiple exostoses neuroblastoma
2135	exostosin like glycosyltransferase 2	EXTL2 Aliases: alpha-1,4-N-acteylhexosaminyltransferase	Homo sapiens (human)	autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 cancer chronic kidney disease hereditary multiple exostoses mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIC mucopolysaccharidosis osteopetrosis osteosclerosis
2137	exostosin like glycosyltransferase 3	EXTL3 Aliases: REG receptor REGR botv glucuronyl-galactosyl-proteoglycan 4-alpha-N-acetylglucosaminyltransferase	Homo sapiens (human)	MHC class II deficiency acute myeloid leukemia adenosine deaminase deficiency agnosia arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 bacterial sepsis brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cherubism chondrodysplasia punctata ciliary body disease cocaine abuse cocaine dependence colorectal cancer colorectal carcinoma coronary artery disease developmental coordination disorder endometriosis of uterus endometriosis epithelioid sarcoma exostosis giant cell glioblastoma glioblastoma head and neck cancer head and neck squamous cell carcinoma hereditary multiple exostoses hypereosinophilic syndrome intellectual disability iris disease large intestine cancer learning disability liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphopenia morphine dependence mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIC mucopolysaccharidosis multiple epiphyseal dysplasia nutmeg liver osteochondrodysplasia osteopetrosis osteosclerosis panuveitis periarthritis pulmonary embolism sarcoma scoliosis secondary syphilis severe combined immunodeficiency spindle cell sarcoma tendinitis tuberculosis uveitis
2224	farnesyl diphosphate synthase	FDPS Aliases: farnesyl pyrophosphate synthetase, dimethylallyltranstransferase, geranyltranstransferase	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 Chagas disease Pick's disease Plasmodium falciparum malaria Reye syndrome Werner syndrome anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis bone disease bone osteosarcoma brain cancer brain disease cancer cartilage disease cerebral degeneration chronic obstructive pulmonary disease colitis colon cancer colonic benign neoplasm congestive heart failure connective tissue disease coronary artery disease cutaneous leishmaniasis depressive disorder diabetes mellitus diabetic ketoacidosis dysthymic disorder embryoma gastroenteritis generalized anxiety disorder giant cell glioblastoma glioblastoma gonorrhea heart valve disease high grade glioma ileitis ileocolitis intestinal infectious disease leech infestation lymphoid leukemia major depressive disorder malignant fibrous histiocytoma melancholic depression melanoma microphthalmia multiple myeloma myeloid leukemia myiasis neurodegenerative disease neurotic disorder nutmeg liver obesity obsolete Matthew-Wood syndrome obsolete melancholia osteoporosis osteosarcoma pancreatic cancer pancreatic carcinoma phobic disorder photosensitive epilepsy photosensitivity disease pneumonia porokeratosis progeria prostate cancer prostate carcinoma pulmonary emphysema sickle cell anemia skin melanoma squamous cell carcinoma thyroid gland anaplastic carcinoma tongue squamous cell carcinoma toxoplasmosis trypanosomiasis type 2 diabetes mellitus
2222	farnesyl-diphosphate farnesyltransferase 1	FDFT1 Aliases: SQS squalene synthase	Homo sapiens (human)	Smith-Lemli-Opitz syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 acrodermatitis adenocarcinoma adenoma bronchus cancer bronchus carcinoma cancer cannabis abuse cannabis dependence cardiovascular system disease cataract chondrodysplasia punctata cocaine abuse cocaine dependence cribriform carcinoma dermatitis embryoma epilepsy familial hyperlipidemia familial mediterranean fever giant cell glioblastoma glioblastoma granular cell carcinoma heart disease hepatocellular carcinoma high grade glioma intellectual disability learning disability liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma melanoma mevalonic aciduria morbid obesity morphine dependence obesity phencyclidine abuse prostate cancer prostate carcinoma skin disease skin melanoma steatotic liver disease tubular adenocarcinoma visual cortex disease visual epilepsy
2171	fatty acid binding protein 5	FABP5	Homo sapiens (human)	prostate cancer psoriasis
3992	fatty acid desaturase 1	FADS1 Aliases: D5D FADS6 FADSD5 TU12 acyl-CoA (8-3)-desaturase delta-5 desaturase	Homo sapiens (human)	Crohn's colitis Crohn's disease abdominal obesity-metabolic syndrome 1 acute chest syndrome acute lymphoblastic leukemia adult acute lymphocytic leukemia age related macular degeneration alcohol use disorder allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atrial fibrillation attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bipolar I disorder bipolar disorder bone osteosarcoma borderline personality disorder breast cancer breast carcinoma cancer cardiovascular system disease cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia childhood osteosarcoma chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease degeneration of macula and posterior pole depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis embryoma essential hypertension gestational diabetes heart disease hepatocellular carcinoma hypertension inflammatory bowel disease 1 inflammatory bowel disease intermittent explosive disorder intrinsic asthma kwashiorkor large intestine cancer laryngeal squamous cell carcinoma liver cancer liver cirrhosis lung benign neoplasm lung carcinoma macular degeneration major depressive disorder marasmus melancholic depression neurotic disorder nutmeg liver nutrition disease obesity obsolete melancholia osteosarcoma pancreatic cancer pancreatic carcinoma polycystic ovary syndrome progressive pseudorheumatoid arthropathy of childhood protein-energy malnutrition rheumatoid arthritis schizophrenia steatotic liver disease stomach cancer stomach carcinoma type 2 diabetes mellitus ulcerative colitis vitiligo
9415	fatty acid desaturase 2	FADS2 Aliases: D6D DES6 FADSD6 SLL0262 TU13 delta-6-desaturase	Homo sapiens (human)	Crohn's colitis Crohn's disease Fabry disease Wolman disease abdominal obesity-metabolic syndrome 1 acquired immunodeficiency syndrome acute myocardial infarction age related macular degeneration alcohol use disorder allergic asthma alopecia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease asthma atherosclerosis atopic dermatitis atrial fibrillation attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bipolar I disorder bipolar disorder breast cancer breast carcinoma cancer cardiovascular system disease cerebral infarction cerebrovascular disease chronic kidney disease chylomicron retention disease colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism congestive heart failure coronary artery disease coronary thrombosis degeneration of macula and posterior pole depressive disorder dermatitis diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy discrete subaortic stenosis embryoma giant cell glioblastoma glioblastoma glomerulonephritis heart disease hemochromatosis type 1 hemochromatosis hepatitis hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hypothyroidism inflammatory bowel disease 1 inflammatory bowel disease intrinsic asthma kidney disease kwashiorkor large intestine cancer laryngeal squamous cell carcinoma lipid metabolism disorder lipid storage disease liver cancer lung benign neoplasm lung carcinoma macular degeneration major depressive disorder marasmus melancholic depression myocardial infarction myxedema nephritis nephrosis neurotic disorder nutmeg liver nutrition disease obesity obsolete melancholia polycystic ovary syndrome progressive pseudorheumatoid arthropathy of childhood protein-energy malnutrition psoriatic arthritis pyoureter rheumatoid arthritis schizophrenia silent myocardial infarction skin disease steatotic liver disease stomach cancer stomach carcinoma type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis vitiligo
2194	fatty acid synthase	FASN Aliases: 3-hydroxyacyl-[acyl-carrier-protein] dehydratase 3-oxoacyl-[acyl-carrier-protein] reductase 3-oxoacyl-[acyl-carrier-protein] synthase Acyl-[acyl-carrier-protein] hydrolase Enoyl-[acyl-carrier-protein] reductase FAS SDR27X1 [Acyl-carrier-protein] S-acetyltransferase [Acyl-carrier-protein] S-malonyltransferase short chain dehydrogenase/reductase family 27X, member 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 B-cell lymphoma Barrett's esophagus Japanese encephalitis Marinesco-Sjogren syndrome Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Niemann-Pick disease type C1 Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome X-linked dilated cardiomyopathy Zollinger-Ellison syndrome acoustic neuroma acute chest syndrome adenocarcinoma adenoma adrenal gland hyperfunction adult liposarcoma adult oligodendroglioma agnosia angiomatous meningioma arrhythmogenic right ventricular cardiomyopathy arthritis arthropathy autoimmune lymphoproliferative syndrome bacterial sepsis basal cell carcinoma benign breast phyllodes tumor benign meningioma bladder carcinoma blindness bone cancer bone osteosarcoma brain cancer breast cancer breast carcinoma breast malignant phyllodes tumor bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy central nervous system cancer cerebral convexity meningioma cerebral degeneration chikungunya childhood liposarcoma childhood oligodendroglioma childhood osteosarcoma chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia clear cell meningioma clear cell renal cell carcinoma clubfoot colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma cone-rod dystrophy congenital hypothyroidism congestive heart failure cribriform carcinoma dedifferentiated liposarcoma dengue disease dengue hemorrhagic fever depressive disorder diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma 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 dysplastic nevus syndrome embryoma encephalitis encephalomyelitis endometrial adenocarcinoma endometrial cancer endometrial carcinoma endomyocardial fibrosis epithelioid leiomyosarcoma esophageal cancer esophageal carcinoma esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension familial hyperlipidemia familial hypertrophic cardiomyopathy familial retinoblastoma fibrous meningioma fundus albipunctatus gastric adenocarcinoma gastrointestinal stromal tumor gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma granular cell tumor head and neck cancer hepatitis B hepatitis C hepatocellular carcinoma herpes simplex high grade glioma hyperglycemia hyperinsulinism hypertension hypertrophic cardiomyopathy hypothyroidism idiopathic interstitial pneumonia inflammatory bowel disease 1 inflammatory bowel disease inflammatory liposarcoma intellectual disability intraorbital meningioma intraventricular meningioma kidney cancer large intestine cancer learning disability leiomyoma leiomyosarcoma leukemia leukopenia liposarcoma liver cancer liver carcinoma luminal breast carcinoma A lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoplasmacyte-rich meningioma mantle cell lymphoma melanoma meningioma meningothelial meningioma metabolic dysfunction-associated steatotic liver disease microcystic meningioma microinvasive gastric cancer microphthalmia mixed glioma mixed oligodendroglioma-astrocytoma multiple myeloma muscular disease myelitis myofibroma myotonic dystrophy type 1 myotonic dystrophy type 2 myxedema myxoid leiomyosarcoma nasopharynx carcinoma neurofibromatosis obesity obsolete Cushing's syndrome obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma ocular cancer olfactory groove meningioma oligodendroglioma osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary renal cell carcinoma parasagittal meningioma patent ductus arteriosus pituitary adenoma pleomorphic adenoma carcinoma pleomorphic adenoma pleomorphic liposarcoma polycystic kidney disease 3 postinflammatory pulmonary fibrosis primary cerebellar degeneration primary hyperaldosteronism primary immunodeficiency disease prostate adenocarcinoma prostate cancer prostate carcinoma psammomatous meningioma pulmonary fibrosis renal carcinoma renal cell carcinoma renal osteodystrophy retinitis pigmentosa retinoblastoma rippling muscle disease 2 sarcomatoid carcinoma sclerosing liposarcoma sebaceous carcinoma secretory meningioma skin melanoma speech-language disorder-1 spinal meningioma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma sweat gland cancer thyroid gland papillary carcinoma tongue squamous cell carcinoma transitional cell carcinoma transitional meningioma trilateral retinoblastoma tuberculosis 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 ulcerative colitis urinary bladder cancer uterine corpus cancer uterine fibroid varicocele vestibular schwannomatosis viral infectious disease well-differentiated liposarcoma yellow fever
84188	fatty acyl-CoA reductase 1	FAR1 Aliases: FLJ22728 SDR10E1 short chain dehydrogenase/reductase family 10E, member 1	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 MASA syndrome Mast syndrome SPOAN syndrome Troyer syndrome dermatitis hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia microcephaly rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata rhizomelic chondrodysplasia punctate type 4

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