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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 **1026 - 1050** of **1582** in total

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Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
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
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
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
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
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
10905	mannosidase alpha class 1A member 2	MAN1A2 Aliases: MAN1B	Homo sapiens (human)	hepatocellular carcinoma liver cancer
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
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
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
4122	mannosidase alpha class 2A member 2	MAN2A2 Aliases: HsT19662 MANA2X	Homo sapiens (human)	attention deficit hyperactivity disorder schizophrenia
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
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
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
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
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
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
7841	mannosyl-oligosaccharide glucosidase	MOGS Aliases: CWH41 DER7 GCS1 glucosidase I processing A-glucosidase I	Homo sapiens (human)	Japanese encephalitis Turner syndrome Zika fever acquired hyperkeratosis actinic keratosis acute lymphoblastic leukemia acute myeloid leukemia adamantinoma agammaglobulinemia ameloblastoma blepharophimosis bronchus cancer bronchus carcinoma cancer cerebral degeneration chronic monocytic leukemia chronic myelomonocytic leukemia congenital disorder of glycosylation In congenital disorder of glycosylation Iq congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIb congenital disorder of glycosylation cystic fibrosis dengue disease epilepsy gonadal dysgenesis holoprosencephaly 1 holoprosencephaly juvenile myelomonocytic leukemia keratoacanthoma lung benign neoplasm lung cancer lung carcinoma lymphoblastic lymphoma malaria melanoma obesity optic atrophy pleomorphic xanthoastrocytoma sensorineural hearing loss skin melanoma viral infectious disease visual epilepsy yellow fever
4326	matrix metallopeptidase 17	MMP17 Aliases: MT4-MMP	Homo sapiens (human)	adenocarcinoma adenoma aortic aneurysm arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis breast adenocarcinoma breast cancer breast carcinoma cancer coronary artery disease cribriform carcinoma embryoma granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma migraine osteoporosis rheumatoid arthritis tubular adenocarcinoma
64386	matrix metallopeptidase 25	MMP25 Aliases: MT6-MMP	Homo sapiens (human)	X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 acoustic neuroma acute pericementitis adult fibrosarcoma aggressive periodontitis amelogenesis imperfecta hypomaturation type 2A2 amelogenesis imperfecta hypomaturation type 2A3 amelogenesis imperfecta hypomaturation type 2A4 amelogenesis imperfecta hypomaturation type 2A5 amelogenesis imperfecta type 1A amelogenesis imperfecta type 1B amelogenesis imperfecta type 1C amelogenesis imperfecta type 1E amelogenesis imperfecta type 1F amelogenesis imperfecta type 1G amelogenesis imperfecta type 1H amelogenesis imperfecta type 2A1 amelogenesis imperfecta type 3A amelogenesis imperfecta type 4 amelogenesis imperfecta anaplastic astrocytoma angiomatous meningioma arthritis arthropathy benign meningioma brain cancer breast cancer breast carcinoma cancer carcinoma cerebral convexity meningioma childhood cerebral astrocytoma clear cell meningioma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer dental fluorosis dentin dysplasia dentinogenesis imperfecta embryoma fibrillary astrocytoma fibrosarcoma fibrous meningioma gemistocytic astrocytoma giant cell glioblastoma glioblastoma in situ carcinoma intraorbital meningioma intraventricular meningioma juvenile pilocytic astrocytoma large intestine cancer laryngeal squamous cell carcinoma malignant astrocytoma melanoma meningioma meningothelial meningioma microcystic meningioma multiple myeloma multiple sclerosis olfactory groove meningioma osteoarthritis parasagittal meningioma periodontosis pilocytic astrocytoma pituitary adenoma protoplasmic astrocytoma psammomatous meningioma rheumatoid arthritis sarcomatoid carcinoma secretory meningioma skin melanoma spinal meningioma stomach cancer stomach carcinoma subependymal giant cell astrocytoma transitional meningioma
4241	melanotransferrin	MELTF Aliases: CD228 FLJ38863 MAP97 MGC4856 MTF1 MTf melanotransferrin membrane-bound transferrin-like protein	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 MHC class II deficiency Pick's disease Reye syndrome Roberts syndrome Zollinger-Ellison syndrome adenosine deaminase deficiency angiomyolipoma astigmatism bone osteosarcoma cancer carcinoma central nervous system cancer cerebral degeneration cerebral primitive neuroectodermal tumor cervical cancer cervix carcinoma childhood osteosarcoma colorectal cancer colorectal carcinoma dysplastic nevus syndrome embryoma gliosarcoma high grade glioma hyperinsulinism large intestine cancer lung adenocarcinoma lung cancer medulloblastoma medulloepithelioma melanoma melanotic neuroectodermal tumor mixed glioma neuroectodermal tumor obsolete SC phocomelia syndrome obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered osteosarcoma polycystic ovary syndrome sarcomatoid carcinoma severe combined immunodeficiency skin melanoma stomach cancer stomach carcinoma supratentorial primitive neuroectodermal tumor
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
129642	membrane bound O-acyltransferase domain containing 2	MBOAT2 Aliases: FLJ14415 FLJ90298 LPLAT13 Lysophospholipid acyltransferase 2 lysophospholipid acyltransferase 13	Homo sapiens (human)	adrenoleukodystrophy
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
10232	mesothelin	MSLN Aliases: CAK1 MPF	Homo sapiens (human)	acoustic neuroma adenocarcinoma adenoma adenosarcoma adult acute lymphocytic leukemia angiomatous meningioma anthracosilicosis asbestosis benign meningioma benign mesothelioma bile duct adenocarcinoma bile duct cancer bile duct carcinoma breast cancer bronchus cancer bronchus carcinoma byssinosis cancer carcinoma cerebral convexity meningioma cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervicitis cervix carcinoma childhood leukemia cholangiocarcinoma chronic salpingo-oophoritis clear cell meningioma colorectal cancer colorectal carcinoma common bile duct neoplasm cribriform carcinoma distal arthrogryposis embryoma endocervicitis endometrial cancer endometrial carcinoma endometrial serous adenocarcinoma essential hypertension fibrous meningioma gastric adenocarcinoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hematologic cancer hepatocellular carcinoma high grade glioma hypertension intrahepatic cholangiocarcinoma intraorbital meningioma intraventricular meningioma kidney failure large intestine cancer liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma malignant mesothelioma malignant pleural mesothelioma meningioma meningothelial meningioma microcystic meningioma microphthalmia mixed glioma nephroblastoma obsolete Matthew-Wood syndrome olfactory groove meningioma ovarian cancer ovarian carcinoma ovary serous adenocarcinoma pancreas disease pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatic ductal carcinoma parasagittal meningioma patent ductus arteriosus pituitary adenoma psammomatous meningioma salivary gland cancer sarcomatoid carcinoma secretory meningioma spinal meningioma stomach cancer stomach carcinoma thymic carcinoma thymoma transitional meningioma tubular adenocarcinoma uterine corpus cancer
65258	metallophosphoesterase 1	MPPE1 Aliases: Cdc1 PGAP5 post-GPI attachment to proteins 5	Homo sapiens (human)	bipolar disorder borderline personality disorder cancer cerebral malaria chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma hepatitis B hepatitis influenza intermittent explosive disorder malaria melanoma papillary renal cell carcinoma pneumonia renal cell carcinoma sarcomatoid renal cell carcinoma skin melanoma

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