GlyCosmos Portal

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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	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 **651 - 675** of **1582** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
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
79143	membrane bound O-acyltransferase domain containing 7	MBOAT7 Aliases: BB1 LPIAT1 LPLAT LPLAT11 hMBOA-7 lysophosphatidylinositol acyltransferase lysophosphatidylinositol acyltransferase 1 lysophospholipid acyltransferase 11 lysophospholipid acyltransferase 7	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 adrenoleukodystrophy agnosia alcoholic hepatitis alcoholic liver cirrhosis attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autosomal recessive intellectual developmental disorder 57 cardiovascular system disease cerebral degeneration choreatic disease chronic kidney disease communicating hydrocephalus depressive disorder developmental coordination disorder diabetes mellitus diabetic ketoacidosis dysthymic disorder dystonia epilepsy focal epilepsy gallbladder disease heart disease hepatitis B hepatitis C hepatitis hepatocellular carcinoma hydrocephalus intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer liver cirrhosis liver disease major depressive disorder melancholic depression microcephaly neurotic disorder obesity obsolete infantile epileptic encephalopathy obsolete melancholia obstructive hydrocephalus partial motor epilepsy senile degeneration of brain steatotic liver disease stereotypic movement disorder stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 type 2 diabetes mellitus visual epilepsy
129642	membrane bound O-acyltransferase domain containing 2	MBOAT2 Aliases: FLJ14415 FLJ90298 LPLAT13 Lysophospholipid acyltransferase 2 lysophospholipid acyltransferase 13	Homo sapiens (human)	adrenoleukodystrophy
154141	membrane bound O-acyltransferase domain containing 1	MBOAT1 Aliases: LPEAT1 LPLAT14 MGC44669 dJ434O11.1 lysophosphatidylethanolamine acyltransferase 1 lysophospholipid acyltransferase 1 lysophospholipid acyltransferase 14	Homo sapiens (human)	brachydactyly-syndactyly syndrome cholestasis
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
8930	methyl-CpG binding domain 4, DNA glycosylase	MBD4 Aliases: MED1	Homo sapiens (human)	Evans' syndrome Hantavirus hemorrhagic fever with renal syndrome Marinesco-Sjogren syndrome abdominal aortic aneurysm achromatopsia acquired color blindness acute monocytic leukemia acute myeloid leukemia adenocarcinoma adenoma aortic aneurysm autistic disorder autoimmune thrombocytopenic purpura biliary atresia bladder carcinoma blue color blindness breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer cervical adenocarcinoma cervical cancer cervix carcinoma colon cancer colon carcinoma colonic benign neoplasm color blindness colorectal cancer colorectal carcinoma cribriform carcinoma disease of metabolism embryoma endometrial cancer endometrial carcinoma esophagus squamous cell carcinoma follicular adenoma gastrointestinal system cancer gliosarcoma granular cell carcinoma hepatocellular carcinoma high grade glioma large intestine cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma microcystic adenoma mixed glioma osteomyelitis papillary adenoma primary cerebellar degeneration red color blindness red-green color blindness rheumatoid arthritis sarcomatoid carcinoma scleroderma stomach cancer stomach carcinoma systemic lupus erythematosus systemic scleroderma temporal arteritis thrombocytopenia due to platelet alloimmunization thrombocytopenia tubular adenocarcinoma urinary bladder cancer uterine corpus cancer uveal melanoma
27430	methionine adenosyltransferase 2 non-catalytic beta subunit	MAT2B	Homo sapiens (human)
10747	MBL associated serine protease 2	MASP2 Aliases: MAP-2 Map19 mannose-binding lectin associated protein 19 mannose-binding lectin-associated serine protease 2 sMAP	Homo sapiens (human)	B-cell lymphoma Burkitt lymphoma Chagas disease Crohn's colitis Crohn's disease Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Kuhnt-Junius degeneration Langerhans-cell histiocytosis Stevens-Johnson syndrome Streptococcus pneumonia angioedema autoimmune disease autoimmune lymphoproliferative syndrome bacterial sepsis cancer cardiac arrest cardiomyopathy cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ chronic fatigue syndrome colorectal cancer colorectal carcinoma complement component 2 deficiency complement component 4a deficiency complement component 4b deficiency complement component 6 deficiency complement component 7 deficiency complement component 9 deficiency complement deficiency cystic fibrosis diabetes mellitus diabetic ketoacidosis diffuse large B-cell lymphoma embryoma encephalomyelitis endomyocardial fibrosis erythema multiforme esophagus squamous cell carcinoma follicular lymphoma frontotemporal dementia glomerulonephritis hepatitis C hepatocellular carcinoma hereditary angioedema hypersensitivity reaction type III disease hypertrophic cardiomyopathy immune system disease inflammatory bowel disease 1 inflammatory bowel disease kidney disease large intestine cancer lepromatous leprosy leprosy liver cancer lymphoma malaria multiple sclerosis nephritis nephrosis non-Hodgkin lymphoma obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma ovarian cancer ovarian carcinoma parapsoriasis pneumonia psoriasis pustulosis of palm and sole pyoureter reticulosarcoma rheumatic fever rheumatoid arthritis sarcoidosis severe acute respiratory syndrome sporotrichosis systemic lupus erythematosus trypanosomiasis tuberculosis 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 type I complement component 8 deficiency type II complement component 8 deficiency ulcerative colitis urinary schistosomiasis viral infectious disease
5648	MBL associated serine protease 1	MASP1 Aliases: C4/C2 activating component of Ra-reactive factor MAP-1 MASP MASP-3 Map44 mannose-binding lectin-associated serine protease 1	Homo sapiens (human)	3MC syndrome 1 3MC syndrome 2 3MC syndrome 3 3MC syndrome 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 Bloch-Sulzberger syndrome Klippel-Feil syndrome Lewy body dementia Marfan syndrome Pick's disease Reye syndrome acute myocardial infarction age related macular degeneration amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 6 arthritis arthropathy atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect atypical hemolytic-uremic syndrome bacterial infectious disease bacterial sepsis blepharophimosis blindness cancer cardiovascular system disease cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervix carcinoma cleft lip cleft palate cleidocranial dysplasia congenital ptosis coronary thrombosis craniosynostosis cryptorchidism cystic fibrosis degeneration of macula and posterior pole diabetes mellitus diabetic ketoacidosis disseminated intravascular coagulation esophagus squamous cell carcinoma gallbladder disease glaucoma glomerulonephritis heart disease hemolytic-uremic syndrome hepatitis C humeroradial synostosis hydronephrosis hypomelanosis of Ito inclusion body myopathy with Paget disease of bone and frontotemporal dementia inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1 intellectual disability isolated cleft palate kidney disease kidney failure learning disability liver cirrhosis liver disease lung squamous cell carcinoma lupus erythematosus macular degeneration microcephaly multiple sclerosis myocardial infarction nephritis omphalocele patent ductus arteriosus patent foramen ovale placental insufficiency prostate cancer prostate carcinoma ptosis pulmonary tuberculosis purpura fulminans radioulnar synostosis rheumatoid arthritis scoliosis sensorineural hearing loss silent myocardial infarction situs inversus spina bifida occulta spondylolisthesis squamous cell carcinoma systemic lupus erythematosus tongue squamous cell carcinoma tuberculosis tuberculous pneumothorax tuberous sclerosis type 2 diabetes mellitus umbilical hernia uremia vascular dementia ventricular septal defect
1432	mitogen-activated protein kinase 14	MAPK14	Homo sapiens (human)	Alzheimer's disease Parkinson's disease anti-basement membrane glomerulonephritis colon cancer colorectal carcinoma diabetic neuropathy gastric adenocarcinoma nasopharynx carcinoma osteoporosis rectum cancer
149175	mannosidase endo-alpha like	MANEAL Aliases: FLJ31434	Homo sapiens (human)	alternating hemiplegia of childhood autonomic neuropathy central nervous system disease nervous system disease neurodegenerative disease
79694	mannosidase endo-alpha	MANEA Aliases: FLJ12838 endomannosidase glycoprotein endo-alpha-1,2-mannosidase mandaselin	Homo sapiens (human)	anxiety disorder autoimmune disease autoimmune lymphoproliferative syndrome breast cancer cancer cocaine abuse cocaine dependence delusional disorder disease of mental health embryoma endocarditis immune system disease infective endocarditis morphine dependence panic disorder paranoid schizophrenia phobic disorder polycystic ovary syndrome psychotic disorder social phobia subacute bacterial endocarditis
4126	mannosidase beta	MANBA Aliases: beta-mannosidase A	Homo sapiens (human)	Fabry disease allergic asthma allergic disease alternating hemiplegia of childhood angiokeratoma ascending cholangitis asthma attention deficit hyperactivity disorder autonomic neuropathy beta-mannosidosis central nervous system disease cholangitis chronic kidney disease chylomicron retention disease colorectal cancer colorectal carcinoma complement deficiency congenital nystagmus dissociated nystagmus epilepsy intellectual disability intrinsic asthma large intestine cancer learning disability lipid storage disease lysosomal storage disease multiple sclerosis nervous system disease obsolete constipation pathologic nystagmus primary biliary cholangitis primary sclerosing cholangitis sarcoidosis sclerosing cholangitis sensorineural hearing loss speech disorder spontaneous ocular nystagmus suppurative cholangitis uveoparotid fever visual epilepsy
4123	mannosidase alpha class 2C member 1	MAN2C1	Homo sapiens (human)	alpha-mannosidosis breast cancer breast carcinoma carcinoma esophageal cancer esophageal carcinoma intellectual disability learning disability post-traumatic stress disorder prostate cancer prostate carcinoma sarcomatoid carcinoma
23324	mannosidase alpha class 2B member 2	MAN2B2 Aliases: EpMAN Epididymis-specific alpha-mannosidase KIAA0935 core-specific lysosomal alpha-1,6-Mannosidase	Homo sapiens (human)	cerebral infarction cerebrovascular disease primary immunodeficiency disease
4125	mannosidase alpha class 2B member 1	MAN2B1 Aliases: LAMAN lysosomal alpha-mannosidase	Homo sapiens (human)	IgA glomerulonephritis Klippel-Feil syndrome age related macular degeneration alpha-mannosidosis aspartylglucosaminuria cerebral degeneration congenital nystagmus degeneration of macula and posterior pole dissociated nystagmus fucosidosis gingival hypertrophy gingival overgrowth glycogen storage disease II hypertrichosis inguinal hernia intellectual disability learning disability lingual-facial-buccal dyskinesia lysosomal storage disease macular degeneration methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency movement disease mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis pathologic nystagmus retinal degeneration sensorineural hearing loss spondylolisthesis spontaneous ocular nystagmus
4122	mannosidase alpha class 2A member 2	MAN2A2 Aliases: HsT19662 MANA2X	Homo sapiens (human)	attention deficit hyperactivity disorder schizophrenia
4124	mannosidase alpha class 2A member 1	MAN2A1 Aliases: GOLIM7 golgi integral membrane protein 7	Homo sapiens (human)	autoimmune disease autoimmune lymphoproliferative syndrome cancer childhood acute lymphocytic leukemia congenital dyserythropoietic anemia type II congenital dyserythropoietic anemia diabetes mellitus embryoma giant cell glioblastoma glioblastoma hepatocellular carcinoma high grade glioma immune system disease liver cancer prostate cancer prostate carcinoma schizophrenia systemic lupus erythematosus type 2 diabetes mellitus
57134	mannosidase alpha class 1C member 1	MAN1C1 Aliases: HMIC	Homo sapiens (human)	cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma nonpapillary renal cell carcinoma papillary renal cell carcinoma pulmonary emphysema renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia
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
4099	myelin associated glycoprotein	MAG	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 Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 4 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease type 5 Charcot-Marie-Tooth disease Guillain-Barre syndrome Kearns-Sayre syndrome Lewy body dementia MASA syndrome Marfan syndrome Mast syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pelizaeus-Merzbacher disease Pick's disease Reye syndrome SPOAN syndrome Troyer syndrome acute myocardial infarction adrenoleukodystrophy agenesis of the corpus callosum with peripheral neuropathy alternating hemiplegia of childhood amyloidosis angioma serpiginosum arteriosclerotic cardiovascular disease astigmatism atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autonomic neuropathy brain stem infarction cancer capillary hemangioma cavernous hemangioma central nervous system cancer central nervous system disease cerebellar ataxia cerebellar disease cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease chorioangioma chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy compartment syndrome congenital diarrhea 5 with tufting enteropathy congenital nystagmus coronary artery disease coronary thrombosis critical illness polyneuropathy demyelinating disease demyelinating polyneuropathy depressive disorder disease of mental health dissociated nystagmus dysthymic disorder embryoma familial multiple nevi flammei gliosarcoma glomus tumor hemangioma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 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 high grade glioma histiocytoid hemangioma hyperopia immune system disease inflammatory and toxic neuropathy intellectual disability intramuscular hemangioma learning disability lesion of sciatic nerve leukodystrophy lymphangioma major depressive disorder melancholic depression melanoma meningoencephalitis middle cerebral artery infarction mixed glioma monoclonal gammopathy of uncertain significance monoclonal paraproteinemia motor peripheral neuropathy multiple sclerosis myocardial infarction nerve compression syndrome nervous system disease neuroblastoma neuromuscular disease neuropathy neurotic disorder obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia optic atrophy optic neuritis pancreatic cancer paraplegia pathologic nystagmus peripheral nervous system disease placental insufficiency plasma cell neoplasm poikiloderma with neutropenia polyneuropathy polyradiculoneuropathy prostate cancer prostate carcinoma psychotic disorder schizophrenia sciatic neuropathy secondary Parkinson disease silent myocardial infarction situs inversus skin melanoma spontaneous ocular nystagmus substance abuse substance-related disorder trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis
140733	mono-ADP ribosylhydrolase 2	MACROD2 Aliases: O-acetyl-ADP-ribose deacetylase MACROD2 dJ631M13.5	Homo sapiens (human)	Crohn's colitis Crohn's disease Kabuki syndrome acquired immunodeficiency syndrome acute myeloid leukemia autism spectrum disorder autistic disorder bipolar I disorder bipolar disorder cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma disease of mental health embryoma essential hypertension hepatocellular carcinoma human immunodeficiency virus infectious disease hypertension hypogonadotropic hypogonadism 21 with or without anosmia inflammatory bowel disease 1 inflammatory bowel disease intellectual disability large intestine cancer learning disability liver cancer malignant fibrous histiocytoma obesity psychotic disorder substance abuse substance-related disorder ulcerative colitis
28992	mono-ADP ribosylhydrolase 1	MACROD1 Aliases: LRP16	Homo sapiens (human)	acute monocytic leukemia atypical chronic myeloid leukemia, BCR-ABL1 negative bipolar disorder breast cancer breast carcinoma cancer cardiovascular system disease childhood leukemia chronic monocytic leukemia colorectal cancer colorectal carcinoma disease of metabolism embryoma endometrial cancer endometrial carcinoma gout heart disease hepatocellular carcinoma large intestine cancer leukemia liver cancer lymphoid leukemia monocytic leukemia myeloid leukemia nicotine dependence pancreatic cancer pancreatic carcinoma prolactinoma uterine corpus cancer

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