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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 "hydrolase activity, acting on glycosyl bonds"

Displaying entries **76 - 100** of **16787** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
10333	toll like receptor 6	TLR6	Homo sapiens (human)	aspergillosis asthma bacterial pneumonia infective endocarditis perinatal necrotizing enterocolitis rhinitis tuberculosis
10591	2'-deoxynucleoside 5'-phosphate N-hydrolase 1	DNPH1 Aliases: dJ330M21.3 rcl	Homo sapiens (human)
10724	O-GlcNAcase	OGA Aliases: MEA5 NCOAT nuclear cytoplasmic O-GlcNAcase and acetyltransferase	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 Fabry disease GM1 gangliosidosis GM2 gangliosidosis, AB variant GM2 gangliosidosis Gaucher's disease Gilles de la Tourette syndrome Lewy body dementia Marfan syndrome Niemann-Pick disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Sandhoff disease Tay-Sachs disease Timothy syndrome abdominal obesity-metabolic syndrome 1 acoustic neuroma acute myocardial infarction alternating hemiplegia of childhood amnestic disorder amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis angiomatous meningioma anterior horn cell disease aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive distal hereditary motor neuronopathy 1 benign meningioma beta thalassemia breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease central nervous system disease cerebral convexity meningioma cerebral degeneration chronic kidney disease chylomicron retention disease clear cell meningioma colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ia congenital disorder of glycosylation type I congestive heart failure connective tissue benign neoplasm coronary artery disease coronary thrombosis cystitis dermatitis diabetes mellitus diabetic ketoacidosis dystonia embryoma encephalitis encephalomyelitis epilepsy epithelioid sarcoma essential hypertension fibrous meningioma gangliosidosis gastroenteritis gastrointestinal system disease gestational diabetes giant cell glioblastoma gingivitis glioblastoma glomerulonephritis glucose intolerance glycoproteinosis heart disease hepatocellular carcinoma hydronephrosis hypertension ileitis ileocolitis intestinal disease intraorbital meningioma intraventricular meningioma kidney disease kidney failure kwashiorkor large intestine cancer lateral sclerosis lingual-facial-buccal dyskinesia lipid storage disease lipoid nephrosis liver cancer liver cirrhosis long QT syndrome 8 lung cancer lung carcinoma lymphoplasmacyte-rich meningioma lysosomal storage disease marasmus membranous glomerulonephritis meningioma meningothelial meningioma microcystic meningioma microphthalmia motor neuron disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IVB mucopolysaccharidosis multiple acyl-CoA dehydrogenase deficiency multiple myeloma myelitis myocardial infarction nephritis nephrosis nervous system disease neurodegenerative disease nutrition disease obesity obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 olfactory groove meningioma ovarian cancer ovarian carcinoma panic disorder parasagittal meningioma pituitary adenoma prediabetes syndrome progressive familial intrahepatic cholestasis 1 progressive muscular atrophy progressive supranuclear palsy protein-energy malnutrition psammomatous meningioma pyoureter renal osteodystrophy retrograde amnesia sarcoma secondary Parkinson disease secretory meningioma silent myocardial infarction situs inversus sphingolipidosis spinal meningioma spindle cell sarcoma tauopathy thalassemia transitional meningioma tricuspid valve stenosis trigonitis tuberous sclerosis 1 tuberous sclerosis 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 visual epilepsy
10825	neuraminidase 3	NEU3	Homo sapiens (human)	Tay-Sachs disease alternating hemiplegia of childhood amnestic disorder autonomic neuropathy cancer carcinoma central nervous system disease chromophobe renal cell carcinoma clear cell adenocarcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer dissociative amnesia embryoma giant cell glioblastoma glioblastoma high grade glioma idiopathic interstitial pneumonia large intestine cancer lung cancer lung non-small cell carcinoma nervous system disease ovarian cancer ovarian carcinoma ovarian clear cell adenocarcinoma ovary adenocarcinoma papillary renal cell carcinoma postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma pulmonary fibrosis renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma
10855	heparanase	HPSE Aliases: HPA HPSE1 HSE1	Homo sapiens (human)	46,XY sex reversal 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 Barrett's esophagus 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 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 3 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 Crohn's colitis Crohn's disease Evans' syndrome Glanzmann's thrombasthenia Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma IgA glomerulonephritis Japanese encephalitis MHC class II deficiency Pick's disease Reye syndrome Sjogren's syndrome X-linked ichthyosis abdominal aortic aneurysm acrodermatitis acute lymphoblastic leukemia acute myocardial infarction acute pancreatitis adenocarcinoma adenoma adenosine deaminase deficiency adrenal gland cancer adult hepatocellular carcinoma adult lymphoma adult medulloblastoma adult oligodendroglioma agenesis of the corpus callosum with peripheral neuropathy ameloblastoma anaplastic astrocytoma anemia antithrombin III deficiency anxiety disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome autoimmune thrombocytopenic purpura basal cell carcinoma benign mesothelioma bile duct adenocarcinoma bile duct carcinoma bipolar disorder bladder carcinoma blood coagulation disease blood platelet disease bone marrow cancer bone osteosarcoma botryoid rhabdomyosarcoma brain cancer breast adenocarcinoma breast cancer breast carcinoma breast lymphoma bronchus cancer bronchus carcinoma cancer carcinoma cardiac arrest cardiomyopathy cardiovascular system disease carotid artery disease central nervous system cancer central nervous system lymphoma central retinal vein occlusion cerebral degeneration cerebral infarction cerebrovascular disease cervical adenocarcinoma cervical cancer cervical squamous cell carcinoma cervix carcinoma cervix uteri carcinoma in situ cherubism childhood cerebral astrocytoma childhood medulloblastoma childhood oligodendroglioma cholangiocarcinoma choriocarcinoma chromophobe renal cell carcinoma chronic ethmoiditis chronic fatigue syndrome chronic kidney disease chronic myeloid leukemia chronic sphenoidal sinusitis clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma corneal disease coronary artery disease coronary thrombosis cribriform carcinoma cutaneous fibrous histiocytoma dengue disease depressive disorder dermatitis dermoid cyst of ovary diabetes mellitus diabetic angiopathy diabetic ketoacidosis duodenum cancer dysthymic disorder embryoma embryonal rhabdomyosarcoma encephalitis encephalomyelitis endometrial cancer endometrial carcinoma endometriosis of uterus endometriosis endomyocardial fibrosis epithelioid sarcoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia exostosis exudative vitreoretinopathy 1 exudative vitreoretinopathy familial cold autoinflammatory syndrome 1 familial cold autoinflammatory syndrome 4 familial cold autoinflammatory syndrome familial nephrotic syndrome fibrillary astrocytoma focal segmental glomerulosclerosis follicular adenoma gallbladder cancer gallbladder carcinoma gastrointestinal system cancer gemistocytic astrocytoma generalized anxiety disorder giant cell glioblastoma gingival fibromatosis glaucoma glioblastoma gliosarcoma glomerulonephritis granular cell carcinoma gray platelet syndrome head and neck cancer head and neck squamous cell carcinoma heart cancer heart disease hepatic veno-occlusive disease hepatitis B hepatitis C hepatocellular carcinoma hepatoerythropoietic porphyria hereditary multiple exostoses hereditary neuropathy with liability to pressure palsies hidradenoma high grade glioma hyperglycemia hypertension hypertrophic cardiomyopathy immune system disease in situ carcinoma inflammatory bowel disease 1 inflammatory bowel disease intrahepatic cholangiocarcinoma invasive ductal carcinoma juvenile pilocytic astrocytoma keratoconjunctivitis sicca keratoconus kidney disease kidney failure large intestine cancer laryngeal squamous cell carcinoma leukemia lipoid nephrosis liver cancer liver cirrhosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus nephritis lymphoid leukemia lymphoma macrocytic anemia major depressive disorder malaria malignant astrocytoma malignant mesothelioma malignant pleural mesothelioma medulloblastoma medullomyoblastoma melancholic depression melanoma melanotic medulloblastoma membranous glomerulonephritis microcystic adenoma migraine mixed glioma mixed oligodendroglioma-astrocytoma motor peripheral neuropathy mucinous adenocarcinoma multiple myeloma multiple sclerosis myelitis myelodysplastic syndrome myeloid leukemia myeloproliferative neoplasm myocardial infarction myoma nasopharynx carcinoma nephritis nephrosis nephrotic syndrome neuroblastoma neurodegenerative disease neuroendocrine carcinoma neuroendocrine tumor neuropathy neurotic disorder nevoid basal cell carcinoma syndrome nodular prostate nonpapillary renal cell carcinoma nutmeg liver obesity obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete inherited blood coagulation disease obsolete melancholia obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oligodendroglioma osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma pancreatitis papillary adenocarcinoma papillary adenoma papillary carcinoma papillary renal cell carcinoma parapsoriasis periarthritis peripheral nervous system disease pheochromocytoma pilocytic astrocytoma placenta cancer platelet-type bleeding disorder 17 platelet-type bleeding disorder 18 porphyria cutanea tarda primary immunodeficiency disease proliferative diabetic retinopathy prostate cancer prostate carcinoma prostatic adenoma protein C deficiency protein S deficiency proteinuria protoplasmic astrocytoma psoriasis pustulosis of palm and sole qualitative platelet defect rabies renal carcinoma renal cell carcinoma retinal disease retinal vein occlusion retinitis retinopathy of prematurity rhabdomyosarcoma rheumatoid arthritis sarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma severe combined immunodeficiency silent myocardial infarction skin melanoma skin papilloma skin tag small intestine cancer spindle cell sarcoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma synovial sarcoma syringoma tendinitis thromboangiitis obliterans thrombocytopenia due to platelet alloimmunization thrombocytopenia thrombophilia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma tongue cancer tongue squamous cell carcinoma tuberculosis tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis urinary bladder cancer urofacial syndrome uterine corpus cancer vascular disease viral infectious disease von Willebrand's disease 1 von Willebrand's disease yellow fever
10905	mannosidase alpha class 1A member 2	MAN1A2 Aliases: MAN1B	Homo sapiens (human)	hepatocellular carcinoma liver cancer
11141	interleukin 1 receptor accessory protein like 1	IL1RAPL1 Aliases: IL1R8 OPHN4 TIGIRR-2	Homo sapiens (human)	B-cell lymphoma Bell's palsy Coffin-Lowry syndrome Klinefelter syndrome Marfan syndrome Meckel's diverticulum Patau syndrome X-linked adrenal hypoplasia congenita allergic asthma asthma attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome brain cancer breast cancer breast carcinoma cancer cardiovascular system disease chromosome Xp21 deletion syndrome clubfoot diffuse large B-cell lymphoma embryoma facial nerve disease facial paralysis heart disease hepatocellular carcinoma immune system disease intellectual disability intrinsic asthma learning disability liver cancer melanoma non-syndromic X-linked intellectual disability 21 non-syndromic X-linked intellectual disability obesity obsolete ymphosarcoma placental insufficiency pyloric stenosis rheumatoid arthritis situs inversus skin melanoma syndromic X-linked intellectual disability 94 tuberous sclerosis visual epilepsy vitiligo
11181	trehalase	TREH Aliases: MGC129621 TRE TREA alpha,alpha-trehalase alpha,alpha-trehalose glucohydrolase	Homo sapiens (human)	adult medulloblastoma autosomal dominant cerebellar ataxia bronchus cancer bronchus carcinoma cancer central nervous system cancer childhood medulloblastoma diabetes mellitus diabetic ketoacidosis diarrhea embryoma familial nephrotic syndrome giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis hepatocellular carcinoma herpes simplex high grade glioma kidney disease lipoid nephrosis liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma medulloblastoma medullomyoblastoma melanotic medulloblastoma mixed glioma nephritis nephrosis nephrotic syndrome type 1 nephrotic syndrome optic atrophy 1 optic atrophy pyoureter rheumatoid arthritis spinal cancer steatotic liver disease type 2 diabetes mellitus
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
11544	ADP-ribosylarginine hydrolase	Adprh	Mus musculus (house mouse)
11722	amylase 1, salivary	Amy1	Mus musculus (house mouse)
11871	ADP-ribosyltransferase 2a	Art2a	Mus musculus (house mouse)
11872	ADP-ribosyltransferase 2b	Art2b	Mus musculus (house mouse)
12091	galactosidase, beta 1	Glb1	Mus musculus (house mouse)	GM1 gangliosidosis type 1 GM1 gangliosidosis type 2 GM1 gangliosidosis type 3 GM1 gangliosidosis mucopolysaccharidosis IV mucopolysaccharidosis type IVB
12182	bone marrow stromal cell antigen 1	Bst1	Mus musculus (house mouse)
12494	CD38 antigen	Cd38	Mus musculus (house mouse)	type 1 diabetes mellitus type 2 diabetes mellitus
12654	chitinase 3 like 1	Chi3l1	Mus musculus (house mouse)	acute myeloid leukemia arteriosclerosis asthma bacterial meningitis breast cancer bronchopulmonary dysplasia chondrosarcoma chronic obstructive pulmonary disease colorectal carcinoma congestive heart failure coronary artery disease endometrial cancer glioblastoma hypertension lung non-small cell carcinoma melanoma multiple myeloma myocardial infarction ovarian cancer pre-eclampsia prostate carcinoma pulmonary fibrosis pulmonary sarcoidosis rheumatoid arthritis schizophrenia small cell carcinoma systemic scleroderma temporal arteritis type 1 diabetes mellitus type 2 diabetes mellitus
12655	chitinase-like 3	Chil3	Mus musculus (house mouse)	asthma sinusitis
12659	oviductal glycoprotein 1	Ovgp1	Mus musculus (house mouse)
14376	alpha glucosidase 2 alpha neutral subunit	Ganab	Mus musculus (house mouse)	polycystic kidney disease 3 polycystic kidney disease polycystic liver disease
14387	glucosidase, alpha, acid	Gaa	Mus musculus (house mouse)	glycogen storage disease II
14420	galactosylceramidase	Galc	Mus musculus (house mouse)	Creutzfeldt-Jakob disease Krabbe disease Mycoplasma pneumoniae pneumonia melanoma
14466	glucosylceramidase beta 1	Gba1	Mus musculus (house mouse)	Gaucher's disease perinatal lethal Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease type IIIC Gaucher's disease Lewy body dementia Netherton syndrome Parkinson's disease Parkinsonism late onset Parkinson's disease psoriasis
14667	GM2 ganglioside activator protein	Gm2a	Mus musculus (house mouse)	GM2 gangliosidosis, AB variant GM2 gangliosidosis
15211	hexosaminidase A	Hexa	Mus musculus (house mouse)	Tay-Sachs disease

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