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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

Search results for "galactosyltransferase activity"

Displaying entries **1 - 25** of **11012** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
28	ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase	ABO Aliases: A3GALNT A3GALT1	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 COVID-19 Chagas disease Chediak-Higashi syndrome Clostridium difficile colitis Crohn's colitis Crohn's disease Evans' syndrome Ewing sarcoma Gilbert syndrome Goodpasture syndrome Graves' disease Hirschsprung's disease IgA glomerulonephritis Japanese encephalitis Kawasaki disease MYH-9 related disease Marfan syndrome Papillon-Lefevre disease Pelger-Huet anomaly Pick's disease Plasmodium falciparum malaria Plasmodium vivax malaria Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia Takayasu's arteritis Waardenburg syndrome type 1 Waardenburg syndrome West Nile fever abdominal aortic aneurysm acquired immunodeficiency syndrome acute biphenotypic leukemia acute chest syndrome acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute myocardial infarction acute promyelocytic leukemia adenocarcinoma adenoma adult acute lymphocytic leukemia adult hepatocellular carcinoma adult lymphoma adult respiratory distress syndrome agammaglobulinemia agranulocytosis alcohol dependence alcohol use disorder allergic asthma allergic disease allergic rhinitis alopecia areata alopecia alternating hemiplegia of childhood anemia anencephaly angioedema angiomyolipoma antithrombin III deficiency anxiety disorder aortitis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy aspergillosis asthma atherosclerosis atopic dermatitis atrial fibrillation atrophic gastritis autistic disorder autoimmune disease autoimmune hemolytic anemia autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura autonomic neuropathy bacterial sepsis bacterial vaginosis bilateral breast cancer bilirubin metabolic disorder bipolar disorder black piedra bladder carcinoma blood group incompatibility brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease central nervous system disease central nervous system lymphoma cerebral degeneration cerebral infarction cerebral primitive neuroectodermal tumor cerebrovascular disease childhood acute lymphocytic leukemia childhood hepatocellular carcinoma childhood leukemia childhood lymphoma cholera choriocarcinoma chronic kidney disease chronic lymphocytic leukemia chronic myeloid leukemia clear cell renal cell carcinoma clitoris cancer coccidioidomycosis colorectal cancer colorectal carcinoma cone-rod dystrophy congenital heart disease congenital hemolytic anemia congestive heart failure contagious pustular dermatitis conversion disorder coronary artery disease coronary thrombosis cowpox crescentic glomerulonephritis cribriform carcinoma cystic fibrosis cystinuria delusional disorder dengue disease dermatitis diabetes mellitus diabetic ketoacidosis diarrhea diffuse large B-cell lymphoma dilated cardiomyopathy 1A dilated cardiomyopathy disease of mental health dissociative disorder duodenal ulcer echinococcosis eclampsia embryoma endometrial cancer endometrial carcinoma endomyocardial fibrosis enterobiasis epilepsy erythema infectiosum esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia exanthema subitum factor VIII deficiency familial adenomatous polyposis familial hypercholesterolemia familial hypertrophic cardiomyopathy familial mediterranean fever fetal erythroblastosis filariasis fundus albipunctatus galactosemia gallbladder carcinoma gastrointestinal system cancer generalized atherosclerosis gestational diabetes gestational trophoblastic neoplasm giant cell glioblastoma glaucoma glioblastoma glomerulonephritis glucose intolerance glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease goiter gonorrhea graft-versus-host disease granular cell carcinoma granulomatosis with polyangiitis heart cancer heart disease hematologic cancer hemoglobin C disease hemoglobin D disease hemoglobin E disease hemoglobinopathy hemolytic anemia hemolytic-uremic syndrome hepatitis B hepatitis C hepatitis hepatocellular carcinoma hereditary angioedema high grade glioma histoplasmosis human immunodeficiency virus infectious disease hypersensitivity vasculitis hypertension hyperthyroidism hypertrophic cardiomyopathy idiopathic scoliosis immune system disease infertility inflammatory bowel disease 1 inflammatory bowel disease influenza insulinoma intermittent claudication intestinal schistosomiasis intracranial vasospasm intrinsic asthma invasive ductal carcinoma islet cell tumor kidney angiomyolipoma kidney cancer kidney disease large intestine cancer leukemia leukopenia liver cancer liver cirrhosis low tension glaucoma lung benign neoplasm lung cancer lung carcinoma lung disease lymphocele lymphoma macrocytic anemia malaria malignant exocrine pancreas neoplasm mastitis medulloblastoma medulloepithelioma melancholic depression mevalonic aciduria microphthalmia milker's nodule mitral valve insufficiency mitral valve prolapse mood disorder multiple endocrine neoplasia type 1 multiple endocrine neoplasia type 2A multiple myeloma multiple sclerosis myelodysplastic syndrome myelomeningocele myocardial infarction nasopharynx carcinoma neonatal anemia neonatal jaundice nephritis nephrosis nervous system disease neuroectodermal tumor neuroendocrine carcinoma neuroendocrine tumor neurotic disorder neutropenia newborn respiratory distress syndrome nontoxic goiter nutmeg liver obesity obsessive-compulsive disorder obsolete Matthew-Wood syndrome obsolete embryonal Tumor with Multilayered Rosettes, C19MC-Altered obsolete major affective disorder 2 obsolete malignant histiocytosis obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oophoritis open-angle glaucoma oral submucous fibrosis osteoarthritis osteoporosis otitis media ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma pancreatic ductal adenocarcinoma pancreatitis parametritis paranoid schizophrenia parasitic helminthiasis infectious disease paratyphoid fever pelvic inflammatory disease peptic ulcer disease perinatal necrotizing enterocolitis peripheral artery disease peripheral vascular disease phobic disorder piebaldism pigment dispersion syndrome placenta cancer placental insufficiency platelet-type bleeding disorder 11 platelet-type bleeding disorder 3 platelet-type bleeding disorder 8 platelet-type bleeding disorder 9 pneumonia polyarteritis nodosa post-thrombotic syndrome postpartum depression postural orthostatic tachycardia syndrome prediabetes syndrome primary biliary cholangitis primary open angle glaucoma progressive familial intrahepatic cholestasis 1 prostate cancer prostate carcinoma protein C deficiency protein S deficiency psychotic disorder pulmonary embolism pulmonary sarcoidosis pure red-cell aplasia pyosalpinx pyoureter rapidly progressive glomerulonephritis rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma respiratory failure retinitis pigmentosa rheumatic fever rheumatoid arthritis rubella salpingitis sarcomatoid carcinoma schistosomiasis schizophrenia severe acute respiratory syndrome severe congenital neutropenia sickle cell anemia silent myocardial infarction situs inversus skin benign neoplasm skin cancer smallpox social phobia spina bifida sporadic breast cancer sporotrichosis squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma superficial mycosis supratentorial primitive neuroectodermal tumor tarsal-carpal coalition syndrome tendinitis tetanus tethered spinal cord syndrome thalassemia thrombocytopenia thrombophilia thrombotic thrombocytopenic purpura thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland disease thyrotoxicosis tongue squamous cell carcinoma transient cerebral ischemia transitional cell carcinoma trichinosis trypanosomiasis tuberous sclerosis 1 tuberous sclerosis tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus typhoid fever ulcerative colitis urinary bladder cancer urinary tract obstruction uterine corpus cancer vaginitis variola major variola minor vascular disease vascular hemostatic disease vasomotor rhinitis viral infectious disease visual epilepsy vitiligo von Willebrand's disease 1 von Willebrand's disease vulva cancer vulva carcinoma vulvitis vulvovaginitis white piedra yellow fever
2683	beta-1,4-galactosyltransferase 1	B4GALT1 Aliases: Beta-N-acetylglucosaminylglycopeptide beta-1,4-galactosyltransferase N-acetyllactosamine synthase beta4Gal-T1 lactose synthase A	Homo sapiens (human)	Dandy-Walker syndrome IgA glomerulonephritis arteriosclerotic cardiovascular disease atherosclerosis bladder carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer childhood leukemia chronic myeloid leukemia colorectal cancer colorectal carcinoma congenital disorder of glycosylation type IId congenital disorder of glycosylation coronary artery disease diabetic ketoacidosis embryoma endocrine system disease familial periodic paralysis hepatitis hepatocellular carcinoma isolated elevated serum creatine phosphokinase levels large intestine cancer leukemia liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma mastitis myopathy obsolete type 1 diabetes mellitus 9 rheumatoid arthritis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus urinary bladder cancer
3906	lactalbumin alpha	LALBA Aliases: HAMLET LYZG LYZL7 lactose synthase B lysozyme G	Homo sapiens (human)	breast cancer breast carcinoma cancer deficiency anemia embryoma eosinophilic esophagitis fibromyalgia gastroenteritis hypochromic anemia liver cirrhosis microcytic anemia milk allergy mitral valve stenosis multiple sclerosis myositis obesity polycystic ovary syndrome steatotic liver disease
7368	UDP glycosyltransferase 8	UGT8 Aliases: 2-hydroxyacylsphingosine 1-beta-galactosyltransferase	Homo sapiens (human)	Barrett's esophagus GM2 gangliosidosis adenocarcinoma adenoma adult oligodendroglioma adult respiratory distress syndrome allergic rhinitis anthracosilicosis anthracosis asbestosis brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer childhood oligodendroglioma classic galactosemia congenital hemolytic anemia cribriform carcinoma cystinuria dilated cardiomyopathy 1A dilated cardiomyopathy embryoma epilepsy esophagus adenocarcinoma favism galactokinase deficiency galactosemia gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease granular cell carcinoma hepatocellular carcinoma hereditary elliptocytosis high grade glioma liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma melanoma mixed glioma mixed oligodendroglioma-astrocytoma myotonic disease myotonic dystrophy type 1 myotonic dystrophy type 2 newborn respiratory distress syndrome oligodendroglioma pancreatic cancer pancreatic carcinoma parapsoriasis parietal foramina prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole skin melanoma split hand-foot malformation 1 split hand-foot malformation 2 split hand-foot malformation 3 split hand-foot malformation 4 split hand-foot malformation 5 split hand-foot malformation 6 split hand-foot malformation tubular adenocarcinoma vasomotor rhinitis visual epilepsy
8702	beta-1,4-galactosyltransferase 4	B4GALT4 Aliases: beta4Gal-T4	Homo sapiens (human)	prostate cancer prostate carcinoma
8703	beta-1,4-galactosyltransferase 3	B4GALT3 Aliases: beta4Gal-T3	Homo sapiens (human)	bladder carcinoma cancer cervical adenocarcinoma cervical cancer cervix carcinoma colorectal cancer colorectal carcinoma embryoma large intestine cancer neuroblastoma primary open angle glaucoma urinary bladder cancer
8704	beta-1,4-galactosyltransferase 2	B4GALT2 Aliases: Beta-N-acetylglucosaminylglycopeptide beta-1,4-galactosyltransferase N-acetyllactosamine synthase beta4Gal-T2 lactose synthase A	Homo sapiens (human)	attention deficit hyperactivity disorder cervical cancer colorectal cancer colorectal carcinoma diabetic cataract diabetic retinopathy large intestine cancer
8705	beta-1,3-galactosyltransferase 4	B3GALT4 Aliases: GalT4 beta3Gal-T4 ganglioside galactosyltransferase	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 Ehlers-Danlos syndrome Parkinson's disease Pick's disease Reye syndrome breast cancer cerebral degeneration colorectal cancer colorectal carcinoma large intestine cancer late onset Parkinson's disease osteogenesis imperfecta
8706	beta-1,3-N-acetylgalactosaminyltransferase 1 (Globoside blood group)	B3GALNT1 Aliases: B3GALANT1 GLOB P antigen synthase beta3Gal-T3 galT3 globoside synthase	Homo sapiens (human)	brain cancer cancer lung cancer lung non-small cell carcinoma pancreatic ductal adenocarcinoma
8707	beta-1,3-galactosyltransferase 2	B3GALT2 Aliases: beta3Gal-T2	Homo sapiens (human)
8708	beta-1,3-galactosyltransferase 1	B3GALT1 Aliases: beta3Gal-T1	Homo sapiens (human)	Peters plus syndrome adenocarcinoma adenoma cribriform carcinoma granular cell carcinoma tubular adenocarcinoma
8985	procollagen-lysine,2-oxoglutarate 5-dioxygenase 3	PLOD3 Aliases: LH3 Multifunctional procollagen lysine hydroxylase and glycosyltransferase LH3 lysyl hydroxlase 3	Homo sapiens (human)	bone disease bronchus cancer bronchus carcinoma cancer cartilage disease cataract central nervous system cancer central nervous system lymphoma clubfoot collagen disease congenital hypothyroidism connective tissue disease diaphragmatic eventration embryoma epidermolysis bullosa simplex Dowling-Meara type epidermolysis bullosa simplex Ogna type epidermolysis bullosa simplex with muscular dystrophy epidermolysis bullosa simplex epidermolysis bullosa esophageal cancer esophageal carcinoma gamma-glutamyl transpeptidase deficiency giant cell glioblastoma glioblastoma gliosarcoma hepatocellular carcinoma high grade glioma hypothyroidism liver cancer lung benign neoplasm lung cancer lung carcinoma lymphoma mixed glioma myopia myxedema nonsyndromic congenital nail disorder 9 obsolete ymphosarcoma placental insufficiency scoliosis sensorineural hearing loss thoracic aortic aneurysm
9331	beta-1,4-galactosyltransferase 6	B4GALT6 Aliases: UDP-Gal:glucosylceramide beta-1,4-galactosyltransferase beta4GalT-VI	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer multiple sclerosis skin disease
9334	beta-1,4-galactosyltransferase 5	B4GALT5 Aliases: beta4-GalT IV beta4GalT-V	Homo sapiens (human)	cancer central nervous system cancer colorectal cancer colorectal carcinoma diabetes mellitus diabetic ketoacidosis embryoma gliosarcoma high grade glioma large intestine cancer mixed glioma multiple sclerosis obesity type 2 diabetes mellitus
10317	beta-1,3-galactosyltransferase 5	B3GALT5 Aliases: B3GalT-V B3T5 GLCT5 GlcNAc-beta-1,3-galactosyltransferase 5 beta3Gal-T5 homolog of C. elegans Bt toxin resistance gene bre-5	Homo sapiens (human)	acute myeloid leukemia adenocarcinoma adenoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cribriform carcinoma granular cell carcinoma hepatocellular carcinoma large intestine cancer liver cancer pancreatic cancer pancreatic carcinoma tubular adenocarcinoma
10331	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3	B3GNT3 Aliases: B3GN-T3 B3GNT-3 HP10328 beta-1,3-N-acetylglucosaminyltransferase bGnT-3 beta3Gn-T3 putative type II membrane protein transmembrane protein 3	Homo sapiens (human)	cancer cervical adenocarcinoma cervical cancer cervix carcinoma common wart embryoma influenza lung cancer lung non-small cell carcinoma neuroblastoma
10678	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	B3GNT2 Aliases: B3GN-T1 B3GN-T2 B3GNT-2 BETA3GNT	Homo sapiens (human)	Graves' disease Walker-Warburg syndrome acute myocardial infarction cancer congenital muscular dystrophy-dystroglycanopathy type A1 coronary thrombosis hyperthyroidism myocardial infarction parapsoriasis prostate cancer prostate carcinoma psoriasis pustulosis of palm and sole schizophrenia silent myocardial infarction thyrotoxicosis transitional cell carcinoma
11285	beta-1,4-galactosyltransferase 7	B4GALT7 Aliases: XGALT-1 beta4Gal-T7 galactosyltransferase I	Homo sapiens (human)	Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome Hailey-Hailey disease IgA glomerulonephritis Laron syndrome Larsen-like syndrome B3GAT3 type Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Rothmund-Thomson syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome achondroplasia aortic valve disease 2 aortic valve stenosis arthritis arthropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive Robinow syndrome 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 bone disease cartilage disease chondrodysplasia-pseudohermaphroditism syndrome cleidocranial dysplasia clubfoot colitis collagen disease coloboma congenital disorder of glycosylation type IId congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 connective tissue disease cryptorchidism cutis laxa enophthalmos gastroenteritis gingivitis hepatocellular carcinoma humeroradial synostosis ileitis ileocolitis lipoatrophic diabetes mellitus lipodystrophy liver cancer mal de Meleda microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II mucopolysaccharidosis IV multiple epiphyseal dysplasia obsolete exophthalmos orbital disease osteoarthritis osteochondrodysplasia osteogenesis imperfecta pulmonary valve stenosis radioulnar synostosis restrictive dermopathy rheumatoid arthritis scoliosis skin disease spermatic cord torsion trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
14594	glycoprotein galactosyltransferase alpha 1, 3	Ggta1	Mus musculus (house mouse)
14595	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	B4galt1	Mus musculus (house mouse)	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease
16770	lactalbumin, alpha	Lalba	Mus musculus (house mouse)	gastroenteritis
22239	UDP galactosyltransferase 8A	Ugt8a	Mus musculus (house mouse)
23127	collagen beta(1-O)galactosyltransferase 2	COLGALT2 Aliases: KIAA0584 Procollagen galactosyltransferase	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 bone osteosarcoma breast cancer cerebral degeneration hepatitis A hepatitis lung benign neoplasm osteoarthritis osteosarcoma
24390	beta-1,4-galactosyltransferase 1	B4galt1	Rattus norvegicus (Norway rat)	congenital disorder of glycosylation type IId congenital disorder of glycosylation
24528	lactalbumin, alpha	Lalba	Rattus norvegicus (Norway rat)	gastroenteritis

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