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 **551 - 575** of **1582** in total

« First

‹ Prev

…

19

20

21

22

23

24

25

26

27

…

Next ›

Last »
Gene ID	Gene Name ▼	Gene Symbol	Organism	Disease Ontology
11253	mannosidase alpha class 1B member 1	MAN1B1 Aliases: ER alpha 1,2-mannosidase ERMan1 ERManI MANA-ER MRT15 Man9GlcNAc2-specific processing alpha-mannosidase alpha 1,2-mannosidase endoplasmic Reticulum Class I alpha-mannosidase endoplasmic reticulum alpha-mannosidase 1 endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase 1	Homo sapiens (human)	Hailey-Hailey disease Rafiq syndrome Rothmund-Thomson syndrome agnosia alpha 1-antitrypsin deficiency autistic disorder 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 bladder carcinoma bulimia nervosa cancer cerebral degeneration choreatic disease congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation cutis laxa depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy focal epilepsy gallbladder disease hepatocellular carcinoma hyperopia intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer liver disease major depressive disorder mal de Meleda melancholic depression microcephaly neurotic disorder non-syndromic intellectual disability obsolete infantile epileptic encephalopathy obsolete melancholia oophoritis parametritis partial motor epilepsy pelvic inflammatory disease periventricular nodular heterotopia pyosalpinx restrictive dermopathy salpingitis stereotypic movement disorder syndactyly syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 urinary bladder cancer visual epilepsy
10905	mannosidase alpha class 1A member 2	MAN1A2 Aliases: MAN1B	Homo sapiens (human)	hepatocellular carcinoma liver cancer
4121	mannosidase alpha class 1A member 1	MAN1A1	Homo sapiens (human)	Gaucher's disease acquired immunodeficiency syndrome breast cancer cancer congenital disorder of glycosylation Ih congenital disorder of glycosylation type I congenital disorder of glycosylation diabetes mellitus human immunodeficiency virus infectious disease ovarian cancer ovarian carcinoma type 2 diabetes mellitus
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
4074	mannose-6-phosphate receptor, cation dependent	M6PR Aliases: CD-M6PR CD-MPR	Homo sapiens (human)	cancer depressive disorder dysthymic disorder embryoma major depressive disorder melancholic depression neurotic disorder obsolete melancholia prostate cancer prostate carcinoma
4360	mannose receptor C-type 1	MRC1 Aliases: CD206 CLEC13D CLEC13DL bA541I19.1 macrophage mannose receptor	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 Behcet's disease CD40 ligand deficiency CREST syndrome Clouston syndrome Down syndrome Duchenne muscular dystrophy EEC syndrome Evans' syndrome Ewing sarcoma Fanconi anemia complementation group A Fanconi anemia Guillain-Barre syndrome Hantavirus hemorrhagic fever with renal syndrome 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 Japanese encephalitis Leigh disease Lynch syndrome Marfan syndrome Marinesco-Sjogren syndrome Miller Fisher syndrome Muir-Torre syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome Sjogren-Larsson syndrome Sveinsson chorioretinal atrophy T-cell acute lymphoblastic leukemia X-linked hyper IgM syndrome X-linked ichthyosis abdominal obesity-metabolic syndrome 1 acquired hyperkeratosis acquired immunodeficiency syndrome acrodermatitis actinic keratosis adenocarcinoma adenoma adenosarcoma adult T-cell leukemia/lymphoma adult lymphoma alcoholic hepatitis allergic asthma allergic contact dermatitis amyotrophic lateral sclerosis anaplastic astrocytoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy aseptic meningitis aspergillosis asthma atherosclerosis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura autosomal dominant pseudohypoaldosteronism type 1 autosomal recessive pseudohypoaldosteronism type 1 bacterial sepsis basal cell carcinoma benign giant cell tumor benign mesothelioma bile duct adenocarcinoma bile duct carcinoma bipolar disorder black piedra bladder carcinoma bladder urothelial carcinoma brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma bulbar polio bullous pemphigoid cancer carcinoma cardiovascular system disease central nervous system cancer central nervous system lymphoma cerebral degeneration cerebral infarction cerebral palsy cerebral primitive neuroectodermal tumor cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma childhood cerebral astrocytoma childhood leukemia childhood lymphoma childhood testicular germ cell tumor childhood type dermatomyositis cholangiocarcinoma cholesteatoma choriocarcinoma chromophobe renal cell carcinoma chronic interstitial cystitis chronic lymphocytic leukemia chronic myeloid leukemia chronic obstructive pulmonary disease clear cell renal cell carcinoma clear cell sarcoma cleft palate coccidioidomycosis colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common variable immunodeficiency common wart complement deficiency congestive heart failure coronary artery disease craniosynostosis crescentic glomerulonephritis cribriform carcinoma cutaneous Paget's disease deafness-dystonia-optic neuronopathy syndrome dengue disease dermatitis dermatomyositis diabetes mellitus dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism distal arthrogryposis duodenum cancer dysplastic nevus syndrome ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 embryoma encephalitis encephalomyelitis endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometrial hyperplasia endometrioid ovary carcinoma endometriosis of uterus endometriosis epilepsy epithelioid leiomyosarcoma epithelioid sarcoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma exanthema subitum factor VIII deficiency fallopian tube cancer fallopian tube carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis female reproductive organ cancer fibrillary astrocytoma follicular adenoma gastroenteritis gastroparesis gemistocytic astrocytoma gestational trophoblastic neoplasm giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart cancer heart disease hematologic cancer hemiplegia hepatitis A hepatitis B hepatitis C hepatocellular carcinoma hereditary breast ovarian cancer syndrome herpes simplex high grade glioma histoplasmosis human immunodeficiency virus infectious disease hyper IgM syndrome idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileitis ileocolitis immune system disease immunodeficiency with hyper IgM type 3 in situ carcinoma inflammatory bowel disease influenza inherited metabolic disorder insulinoma interstitial cystitis interstitial lung disease intrahepatic cholangiocarcinoma intrinsic asthma islet cell tumor isolated cleft palate juvenile pilocytic astrocytoma keratoacanthoma kidney cancer large intestine cancer laryngeal disease leiomyosarcoma leishmaniasis leprosy leukemia liver cancer liver carcinoma lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung oat cell carcinoma lung small cell carcinoma lupus erythematosus lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 malignant astrocytoma malignant mesothelioma malignant teratoma mantle cell lymphoma mature teratoma measles medulloblastoma medulloepithelioma melanoma microcystic adenoma microphthalmia mixed glioma morbid obesity mucinous adenocarcinoma multiple myeloma mumps muscular dystrophy myelitis myositis myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 myxoid leiomyosarcoma nasopharynx carcinoma nephroblastoma neuroblastoma neurodegenerative disease neuroectodermal tumor neurofibromatosis 1 neurofibromatosis nodular prostate nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome obsolete T-cell lymphoblastic leukemia/lymphoma obsolete congenital ichthyosiform erythroderma obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete ymphosarcoma osteoarthritis ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma papillary adenocarcinoma papillary adenoma papillary renal cell carcinoma parapsoriasis pemphigus vulgaris pemphigus penis carcinoma in situ penis carcinoma periampullary adenocarcinoma pilocytic astrocytoma placenta cancer pneumocystosis pneumonia poliomyelitis polyp of middle ear postinflammatory pulmonary fibrosis primary cerebellar degeneration primary pulmonary hypertension progressive muscular atrophy prostate cancer prostate carcinoma prostatic adenoma protoplasmic astrocytoma prune belly syndrome pseudohypoaldosteronism psoriasis pulmonary fibrosis pulmonary tuberculosis pustulosis of palm and sole rapidly progressive glomerulonephritis rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma rheumatoid arthritis rubella sarcoidosis sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma sebaceous gland neoplasm seminoma situs inversus skin benign neoplasm skin cancer skin carcinoma skin melanoma small intestine adenocarcinoma small intestine cancer small intestine carcinoma spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spindle cell sarcoma sporadic breast cancer sporotrichosis squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma superficial mycosis supratentorial primitive neuroectodermal tumor syndromic X-linked intellectual disability 94 systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic scleroderma tarsal-carpal coalition syndrome teratoma testicular cancer testicular germ cell cancer testis seminoma thrombocytopenia due to platelet alloimmunization thrombocytopenia thymus lymphoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma tracheal disease transitional cell carcinoma transthyretin amyloidosis trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberculosis tuberculous pneumothorax tuberous sclerosis tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer uterine corpus cancer uveoparotid fever viral infectious disease viral meningitis visceral leishmaniasis visual epilepsy white piedra yellow fever
4351	mannose phosphate isomerase	MPI Aliases: mannose-6-phosphate isomerase	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 Zollinger-Ellison syndrome acute myeloid leukemia acute myocardial infarction antithrombin III deficiency anxiety disorder arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant cerebellar ataxia autosomal recessive hypercholesterolemia autosomal recessive polycystic kidney disease blindness blood coagulation disease campomelic dysplasia cancer carbohydrate metabolic disorder cardiovascular system disease celiac disease central nervous system cancer cerebral degeneration chronic kidney disease congenital disorder of glycosylation Ia congenital disorder of glycosylation Ib congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation congestive heart failure coronary artery disease coronary thrombosis craniometaphyseal dysplasia cryptococcosis cystic fibrosis developmental and epileptic encephalopathy 36 diabetes mellitus diabetic ketoacidosis diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy dry eye syndrome egg allergy elephantiasis embryoma epilepsy essential hypertension familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 gallbladder disease generalized anxiety disorder gliosarcoma heart disease hepatitis B high grade glioma hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypoglycemia laryngeal disease liver cirrhosis liver disease lymphedema marasmus mixed glioma myocardial infarction neurotic disorder nutmeg liver obsolete inherited blood coagulation disease phobic disorder placental insufficiency polycystic kidney disease 4 post-traumatic stress disorder postpartum depression protein C deficiency protein S deficiency protein-losing enteropathy schizophrenia silent myocardial infarction spinocerebellar ataxia type 6 steatotic liver disease thrombocytopenia thrombophilia tracheal disease tropical sprue type 2 diabetes mellitus visual epilepsy xerophthalmia
4153	mannose binding lectin 2	MBL2	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 adult acute lymphocytic leukemia Balo concentric sclerosis Bannayan-Riley-Ruvalcaba syndrome Behcet's disease Burkitt lymphoma Chagas disease Clostridium difficile colitis Coronavirus infectious disease Cowden syndrome Crohn's colitis Crohn's disease Cryptococcal meningitis Duchenne muscular dystrophy Evans' syndrome Graves' disease Guillain-Barre syndrome HELLP syndrome Henoch-Schoenlein purpura 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 Japanese encephalitis Kartagener syndrome Kawasaki disease Klebsiella pneumonia Legionnaires' disease Lyme disease Miller Fisher syndrome Pick's disease Plasmodium falciparum malaria Reye syndrome Richter's syndrome Sjogren's syndrome Streptococcus pneumonia Turner syndrome West Nile fever acquired immunodeficiency syndrome acrodermatitis acute interstitial pneumonia acute lymphoblastic leukemia acute myocardial infarction acute pancreatitis acute pericementitis acute poststreptococcal glomerulonephritis acute pyelonephritis adrenoleukodystrophy adult acute lymphocytic leukemia adult lymphoma adult respiratory distress syndrome age related macular degeneration aggressive periodontitis agranulocytosis allergic asthma allergic bronchopulmonary aspergillosis allergic rhinitis amyloidosis anal carcinoma in situ anemia angioedema ankylosing spondylitis anodontia anogenital venereal wart anthracosilicosis anthracosis antiphospholipid syndrome antithrombin III deficiency aortic valve insufficiency arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asbestosis aspergillosis asthma atherosclerosis atopic dermatitis autoimmune disease autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome autoimmune thrombocytopenic purpura autoimmune thyroiditis 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 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 meningitis bacterial pneumonia bacterial sepsis bacterial vaginosis bipolar disorder black piedra bone inflammation disease brain ischemia breast cancer breast carcinoma bronchiectasis bronchiolitis obliterans bronchiolitis bronchitis bronchopneumonia bronchopulmonary dysplasia bronchus cancer bronchus carcinoma cancer candidiasis cardiac arrest cardiomyopathy cardiovascular system disease carotid artery disease cataract 32 multiple types celiac disease central nervous system cancer central nervous system disease central nervous system lymphoma cerebral degeneration cerebral infarction cerebral malaria cerebral palsy cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood B-cell acute lymphoblastic leukemia childhood type dermatomyositis chorioamnionitis chromosome 10q23 deletion syndrome chronic fatigue syndrome chronic kidney disease chronic lymphocytic leukemia chronic obstructive pulmonary disease coccidioidomycosis colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma common cold common variable immunodeficiency common wart complement component 2 deficiency congenital hypothyroidism congenital muscular dystrophy conjunctivitis coronary aneurysm coronary artery disease coronary restenosis coronary thrombosis cryptosporidiosis cystic fibrosis cystitis degeneration of macula and posterior pole dengue disease dengue hemorrhagic fever dental caries dentin caries dermatitis dermatomyositis dermatophytosis diabetes insipidus diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease by infectious agent disseminated intravascular coagulation distal myopathy eclampsia embryoma encephalomyelitis end stage renal disease endometrial cancer endometrial carcinoma endomyocardial fibrosis enterobiasis epilepsy esophagus squamous cell carcinoma essential hypertension facioscapulohumeral muscular dystrophy fetal erythroblastosis filariasis follicular lymphoma fungal infectious disease gallbladder disease gastroenteritis gastrointestinal tularemia gestational diabetes giardiasis gliosarcoma glomerulonephritis glucose intolerance goiter gonadal dysgenesis heart disease hemiplegia hemolytic-uremic syndrome hepatitis B hepatitis C hepatitis hepatocellular carcinoma hereditary angioedema herpes simplex high grade glioma histoplasmosis human immunodeficiency virus infectious disease hypereosinophilic syndrome hyperglycemia hyperhomocysteinemia hypersensitivity vasculitis hypertension hyperthyroidism hypertrophic cardiomyopathy hypothyroidism ileitis ileocolitis immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome immune system disease immunoglobulin alpha deficiency inflammatory bowel disease 1 inflammatory bowel disease influenza intermediate coronary syndrome intestinal schistosomiasis intrinsic asthma invasive aspergillosis irritable bowel syndrome juvenile polyposis syndrome juvenile rheumatoid arthritis keratoconjunctivitis sicca kidney disease kidney failure large intestine cancer legionellosis leishmaniasis lepromatous leprosy leprosy leptospirosis leukemia leukopenia limb-girdle muscular dystrophy liver cancer liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lung disease lung non-small cell carcinoma lupus erythematosus lupus nephritis lymphoblastic lymphoma lymphoma macrocytic anemia macular degeneration malaria membranous glomerulonephritis meningitis meningococcal meningitis miliary tuberculosis mixed glioma multiple myeloma multiple sclerosis muscular dystrophy myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 myositis myxedema narcolepsy nephritis nephrosis nervous system disease neurocirculatory asthenia neurogenic arthropathy neurohypophyseal diabetes insipidus neuropathy neutropenia newborn respiratory distress syndrome non-suppurative otitis media nutmeg liver obesity 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 obsolete ymphosarcoma obstructive lung disease oculopharyngeal muscular dystrophy oral candidiasis osteoporosis otitis media ovarian cancer pancreatitis panic disorder parapsoriasis patent ductus arteriosus pemphigus vulgaris pemphigus perinatal necrotizing enterocolitis periodontal disease periodontitis periodontosis peripheral nervous system disease peripheral vascular disease placental insufficiency pneumonia polymyalgia rheumatica pre-eclampsia prediabetes syndrome primary biliary cholangitis primary ciliary dyskinesia 1 primary ciliary dyskinesia primary cutaneous T-cell non-Hodgkin lymphoma primary immunodeficiency disease primary open angle glaucoma prostate cancer prostate carcinoma protein C deficiency protein S deficiency psoriasis psoriatic arthritis pulmonary fibrosis pulmonary tuberculosis purpura fulminans pustulosis of palm and sole pyoureter renal osteodystrophy respiratory allergy respiratory failure rheumatic fever rheumatoid arthritis rhinitis rippling muscle disease 2 schistosomiasis selective IgA deficiency disease selective IgG deficiency disease sensorineural hearing loss severe acute respiratory syndrome severe congenital neutropenia sickle cell anemia silent myocardial infarction spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spondyloarthropathy spondylosis sporotrichosis stomach cancer stomach carcinoma sudden infant death syndrome superficial mycosis systemic lupus erythematosus systemic primary carnitine deficiency disease temporal arteritis thrombocytopenia thrombophilia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland disease thyrotoxicosis tonsillitis tooth agenesis toxic shock syndrome trichinosis trigonitis trypanosomiasis tuberculosis tuberculous pneumothorax 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 uremia urinary schistosomiasis urinary tract obstruction uterine cancer uterine corpus cancer vaginitis vascular disease vasculitis vasomotor rhinitis viral infectious disease viral meningitis visceral leishmaniasis visual epilepsy vitiligo vulvitis vulvovaginal candidiasis vulvovaginitis white piedra yellow fever
93432	maltase-glucoamylase 2 (putative)	MGAM2	Homo sapiens (human)
8972	maltase-glucoamylase	MGAM Aliases: MGA alpha-glucosidase	Homo sapiens (human)	Duchenne muscular dystrophy Fabry disease Gaucher's disease Gerstmann-Straussler-Scheinker syndrome Gorham's disease Japanese encephalitis adenocarcinoma adenoma amyotrophic lateral sclerosis arteriosclerotic cardiovascular disease atherosclerosis 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 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 brachydactyly type C brachydactyly breast cancer breast carcinoma cancer cardiomyopathy cardiovascular system disease chylomicron retention disease congenital disorder of glycosylation congenital muscular dystrophy coronary artery disease cribriform carcinoma cystic fibrosis cystinuria dengue disease depressive disorder diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy distal myopathy embryoma endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hypertrophic cardiomyopathy familial periodic paralysis galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease granular cell carcinoma heart disease hyperglycemia hypertrophic cardiomyopathy hypoglycemia limb-girdle muscular dystrophy lipid storage disease lysosomal storage disease major depressive disorder melancholic depression muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myotonic dystrophy type 1 myotonic dystrophy type 2 neuromuscular disease nutmeg liver obesity 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 constipation obsolete melancholia oculopharyngeal muscular dystrophy progressive muscular atrophy prolactinoma punctate palmoplantar keratoderma type III rippling muscle disease 2 squamous cell carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus viral infectious disease yellow fever
27349	malonyl-CoA-acyl carrier protein transacylase	MCAT Aliases: FASN2C MCT MCT1 MT NET62 [acyl-carrier-protein] S-malonyltransferase fabD	Homo sapiens (human)	B-cell lymphoma Barrett's esophagus Burkitt lymphoma Langerhans-cell histiocytosis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Richter's syndrome abdominal aortic aneurysm abdominal obesity-metabolic syndrome 1 actinic keratosis acute myeloid leukemia adenocarcinoma adenoma adult lymphoma benign mastocytoma bladder carcinoma bone osteosarcoma borderline personality disorder brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy central nervous system lymphoma cervical adenocarcinoma cervical cancer cervix carcinoma childhood lymphoma childhood osteosarcoma choriocarcinoma chromophobe renal cell carcinoma chronic lymphocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma congestive heart failure cribriform carcinoma depressive disorder diabetes mellitus diffuse large B-cell lymphoma distal arthrogryposis dysthymic disorder embryoma endomyocardial fibrosis epilepsy esophagus adenocarcinoma esophagus squamous cell carcinoma essential hypertension extracutaneous mastocytoma exudative vitreoretinopathy 1 exudative vitreoretinopathy familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 familial medullary thyroid carcinoma follicular lymphoma gastrointestinal stromal tumor gestational diabetes giant cell glioblastoma glioblastoma granular cell carcinoma hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinemic hypoglycemia hypertension hypertrophic cardiomyopathy idiopathic generalized epilepsy inflammatory bowel disease insulinoma intermittent explosive disorder invasive ductal carcinoma large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder malaria malignant pleural mesothelioma mast cell neoplasm mastocytosis melancholic depression melanoma microphthalmia multiple endocrine neoplasia type 2A multiple myeloma neuroblastoma neurotic disorder non-Hodgkin lymphoma nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome obsolete melancholia obsolete ymphosarcoma optic atrophy osteomalacia osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma placenta cancer premenstrual tension primary hyperparathyroidism primary pulmonary hypertension prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma reticulosarcoma retinopathy of prematurity rickets sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma thyroid gland medullary carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus urinary bladder cancer urticaria pigmentosa visual epilepsy
23417	malonyl-CoA decarboxylase	MLYCD Aliases: MCD hMCD	Homo sapiens (human)	Castleman disease Kaposi's sarcoma Kimura disease Laron syndrome Marfan syndrome Meesmann corneal dystrophy Schmid metaphyseal chondrodysplasia Senior-Loken syndrome achondroplasia acquired immunodeficiency syndrome acute kidney tubular necrosis adult lymphoma autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome cancer cardiomyopathy central nervous system lymphoma childhood lymphoma choline deficiency disease diabetes mellitus diarrhea endomyocardial fibrosis epilepsy essential hypertension familial hypertrophic cardiomyopathy familial nephrotic syndrome focal segmental glomerulosclerosis glomerulonephritis human immunodeficiency virus infectious disease hypertension hypertrophic cardiomyopathy hypoglycemia inherited metabolic disorder kidney disease lactic acidosis lipoid nephrosis liver cirrhosis lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 macular corneal dystrophy membranous glomerulonephritis metabolic dysfunction-associated steatotic liver disease microphthalmia multicentric Castleman disease nasopharynx carcinoma nephritis nephronophthisis 1 nephronophthisis nephrosclerosis nephrosis nephrotic syndrome normal pressure hydrocephalus obesity obsolete Matthew-Wood syndrome obsolete constipation obsolete ymphosarcoma oral tuberculosis primary immunodeficiency disease pyoureter situs inversus steatotic liver disease systemic Epstein-Barr virus positive T-cell lymphoma of childhood tuberculosis tuberous sclerosis 1 tuberous sclerosis type 2 diabetes mellitus visual epilepsy
10873	malic enzyme 3	ME3 Aliases: malate dehydrogenase (oxaloacetate-decarboxylating) (NADP(+))	Homo sapiens (human)	acute myeloid leukemia breast cancer breast carcinoma cancer idiopathic scoliosis pancreatic cancer pancreatic carcinoma
4200	malic enzyme 2	ME2 Aliases: NAD-dependent malic enzyme, mitochondrial malate dehydrogenase (oxaloacetate-decarboxylating)	Homo sapiens (human)	bipolar disorder cancer embryoma epilepsy generalized epilepsy with febrile seizures plus giant cell glioblastoma glioblastoma high grade glioma idiopathic generalized epilepsy leukemia lung benign neoplasm lung cancer lung non-small cell carcinoma microphthalmia obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder
4199	malic enzyme 1	ME1 Aliases: NADP-dependent malic enzyme malate dehydrogenase (oxaloacetate-decarboxylating) (NADP(+))	Homo sapiens (human)	Fanconi anemia complementation group A Fanconi anemia adenocarcinoma adenoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral infarction cerebrovascular disease cholangiocarcinoma clear cell renal cell carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure cribriform carcinoma depressive disorder diabetes mellitus dysthymic disorder embryoma epilepsy focal epilepsy giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma head and neck squamous cell carcinoma hepatocellular carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma kidney cancer kidney failure large cell carcinoma large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma lung squamous cell carcinoma major depressive disorder malignant teratoma mature teratoma melancholic depression mixed glioma neurotic disorder obesity obsolete melancholia partial motor epilepsy renal carcinoma renal cell carcinoma squamous cell carcinoma teratoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis uterine corpus sarcoma visual epilepsy
4191	malate dehydrogenase 2	MDH2	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 myocardial infarction adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenocortical carcinoma agnosia aniridia brain ischemia bronchiolo-alveolar adenocarcinoma brucellosis cancer carcinoma cerebral degeneration chromophobe renal cell carcinoma clear cell renal cell carcinoma cocaine dependence collecting duct carcinoma congenital adrenal hyperplasia congestive heart failure coronary thrombosis depressive disorder developmental and epileptic encephalopathy 51 diabetes mellitus diabetic ketoacidosis duodenum cancer dysthymic disorder dystonia embryoma endometrial cancer endometrial carcinoma epilepsy gastritis glomerulonephritis heart cancer heroin dependence hypercalcemia hypertensive retinopathy hypertropia kidney disease lung cancer lung non-small cell carcinoma major depressive disorder mechanical strabismus melancholic depression melanoma morphine dependence myocardial infarction nephritis nephrocalcinosis nephrosis neurotic disorder obsolete constipation obsolete melancholia ophthalmoplegia opiate dependence ovarian carcinoma panic disorder papillary renal cell carcinoma paraganglioma pheochromocytoma phosphorus metabolism disease prostate cancer prostate carcinoma proteinuria pyoureter renal carcinoma renal cell carcinoma renal osteodystrophy sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma small intestine cancer strabismus substance abuse substance-related disorder uterine cancer uterine corpus cancer visual epilepsy
4190	malate dehydrogenase 1	MDH1	Homo sapiens (human)	Creutzfeldt-Jakob disease Gerstmann-Straussler-Scheinker syndrome X-linked dilated cardiomyopathy adult respiratory distress syndrome amyotrophic lateral sclerosis cancer cone-rod dystrophy developmental and epileptic encephalopathy 88 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 embryoma fatal familial insomnia fundus albipunctatus lung cancer lung non-small cell carcinoma microphthalmia newborn respiratory distress syndrome obsolete Matthew-Wood syndrome pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma progressive muscular atrophy retinitis pigmentosa schizophrenia
57151	lysozyme like 6	LYZL6 Aliases: LYC1 PRO1485 TKAL754	Homo sapiens (human)
131375	lysozyme like 4	LYZL4 Aliases: LYC4 MGC26768	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 cerebral degeneration
119180	lysozyme like 2	LYZL2	Homo sapiens (human)	dental caries dentin caries
84569	lysozyme like 1	LYZL1 Aliases: LYC2 MGC33408	Homo sapiens (human)
254773	lysozyme g2	LYG2 Aliases: LYGA2 LYGH	Homo sapiens (human)
129530	lysozyme g1	LYG1 Aliases: LYGA1 SALW1939	Homo sapiens (human)	cancer
4069	lysozyme	LYZ Aliases: renal amyloidosis	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 Behcet's disease Burkitt lymphoma Crohn's colitis Crohn's disease Graves' disease Langerhans-cell histiocytosis Meier-Gorlin syndrome 1 Meier-Gorlin syndrome Pick's disease Reye syndrome Shwachman-Diamond syndrome Sjogren's syndrome abdominal obesity-metabolic syndrome 1 acinar cell carcinoma acne acquired immunodeficiency syndrome actinic keratosis acute myeloid leukemia adenocarcinoma adenoid cystic carcinoma adenoma alcohol dependence alcohol use disorder allergic rhinitis alternating hemiplegia of childhood amyloidosis anorexia nervosa aphthous stomatitis arachnoiditis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autoimmune polyendocrine syndrome type 1 autoimmune polyendocrine syndrome autonomic neuropathy bacterial infectious disease bacterial vaginosis biliary tract disease breast cancer breast carcinoma cancer candidiasis celiac disease central nervous system cancer central nervous system disease cerebral degeneration childhood leukemia cholestasis chronic ethmoiditis chronic monocytic leukemia chronic myelomonocytic leukemia chronic sphenoidal sinusitis colitis common cold complement deficiency congestive heart failure coronary artery disease craniosynostosis cribriform carcinoma dacryoadenitis dacryocystitis diabetes mellitus diabetic ketoacidosis diarrhea dysentery egg allergy endocrine exophthalmos essential hypertension exanthem familial hyperlipidemia familial mediterranean fever familial nephrotic syndrome familial visceral amyloidosis follicular adenoma gallbladder disease gastritis gastroduodenal Crohn's disease gastroenteritis gastrointestinal stromal tumor gastrointestinal system disease gingivitis gliosarcoma glomerulonephritis granular cell carcinoma hepatocellular carcinoma high grade glioma human immunodeficiency virus infectious disease hypertension hyperthyroidism hypohidrotic ectodermal dysplasia ileitis ileocolitis immune system disease inflammatory bowel disease 1 inflammatory bowel disease interstitial lung disease intestinal disease intestinal infectious disease jejunoileitis juvenile myelomonocytic leukemia juvenile rheumatoid arthritis keratoconjunctivitis sicca kidney disease kidney failure leukemia lipoid nephrosis liver cancer liver disease malignant fibrous histiocytoma mastitis meningitis mevalonic aciduria microcystic adenoma mixed glioma myeloid sarcoma nephritis nephrosis nephrotic syndrome nervous system disease neuropathy nodular prostate non-Langerhans-cell histiocytosis obsolete malignant histiocytosis obsolete ymphosarcoma obstructive jaundice oral candidiasis oral mucosa leukoplakia papillary adenoma parapsoriasis periodontal disease peripheral nervous system disease polyneuropathy post-traumatic stress disorder proctitis prostatic adenoma proteinuria psoriasis pulmonary tuberculosis purpura pustulosis of palm and sole pyoureter reticulohistiocytic granuloma rheumatoid arthritis salivary gland adenoid cystic carcinoma sarcoidosis seborrheic keratosis shigellosis sickle cell anemia skin disease spiradenoma stomach cancer stomach carcinoma systemic lupus erythematosus thyrotoxicosis tuberculosis tuberculous pneumothorax tubular adenocarcinoma type 2 diabetes mellitus ulcerative colitis uremia ureteral obstruction uveoparotid fever vaginitis vasomotor rhinitis vulvitis vulvovaginitis white sponge nevus
11313	lysophospholipase 2	LYPLA2 Aliases: APT-2 acyl-protein thioesterase 2	Homo sapiens (human)	familial combined hyperlipidemia melanoma skin melanoma

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