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 **251 - 275** of **393515** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
2583	beta-1,4-N-acetyl-galactosaminyltransferase 1	B4GALNT1 Aliases: GD2 synthase, GM2 synthase beta1-4GalNAc-T	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 Henoch-Schoenlein purpura MASA syndrome Mast syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Richter's syndrome SPOAN syndrome Troyer syndrome alternating hemiplegia of childhood androgen insensitivity syndrome autonomic neuropathy breast cancer breast carcinoma cancer cataract central nervous system disease chromophobe renal cell carcinoma chronic lymphocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma coronary artery disease diabetic ketoacidosis dystonia embryoma eunuchism gastrointestinal system cancer giant cell glioblastoma glioblastoma hepatocellular carcinoma 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 hypersensitivity vasculitis hypogonadism intellectual disability intestinal benign neoplasm intestinal cancer learning disability lingual-facial-buccal dyskinesia liver cancer melanoma nervous system disease neuroblastoma nonpapillary renal cell carcinoma obsolete type 1 diabetes mellitus 9 ovarian cancer ovarian carcinoma papillary renal cell carcinoma paraplegia premature menopause pseudobulbar palsy renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma scoliosis skin melanoma 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
2584	galactokinase 1	GALK1	Homo sapiens (human)	cancer cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract classic galactosemia colorectal cancer colorectal carcinoma cutaneous fibrous histiocytoma cystinuria diabetic cataract disease of metabolism epidermolysis bullosa simplex localized type epidermolysis bullosa simplex galactokinase deficiency galactose epimerase deficiency galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hepatocellular carcinoma hidradenoma inherited metabolic disorder junctional epidermolysis bullosa non-Herlitz type junctional epidermolysis bullosa with pyloric atresia junctional epidermolysis bullosa large intestine cancer liver cancer placental insufficiency senile cataract skin papilloma skin tag syringoma
2585	galactokinase 2	GALK2 Aliases: GK2	Homo sapiens (human)	bronchus cancer bronchus carcinoma dental caries dentin caries lung adenocarcinoma lung cancer lung carcinoma
2588	galactosamine (N-acetyl)-6-sulfatase	GALNS Aliases: GALNAC6S GAS GalN6S Morquio syndrome N-acetylgalactosamine-6-sulfatase chondroitinase chondroitinsulfatase galactose-6-sulfate sulfatase mucopolysaccharidosis type IVA	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 GM1 gangliosidosis Laron syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome Wilson disease achondroplasia acne adenine phosphoribosyltransferase deficiency adenocarcinoma adenoma age related macular degeneration amyloidosis anthrax disease anxiety disorder arachnoiditis bacterial meningitis bacterial sepsis bacterial vaginosis bile duct adenocarcinoma bile duct carcinoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease cerebral degeneration cholangiocarcinoma chronic lymphocytic leukemia chronic obstructive pulmonary disease chronic ulcer of skin colorectal cancer colorectal carcinoma cribriform carcinoma degeneration of macula and posterior pole dental caries dentin caries diabetes mellitus diabetic ketoacidosis disease of mental health disease of metabolism embryoma enterocele generalized anxiety disorder glomerulonephritis granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hemochromatosis hole retinal cyst impetigo influenza inguinal hernia intrahepatic cholangiocarcinoma iron metabolism disease kidney disease large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lysosomal storage disease macular degeneration macular holes mastitis meningitis metachromatic leukodystrophy mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis VI mucopolysaccharidosis type IVB mucopolysaccharidosis multiple epiphyseal dysplasia myositis necrotizing fasciitis nephritis osteochondrodysplasia osteoporosis pharyngitis phobic disorder prostate cancer prostate carcinoma psychotic disorder pyoderma retinal perforation rheumatic fever scarlet fever scoliosis sensorineural hearing loss stomach cancer stomach carcinoma tonsillitis tuberculosis tubular adenocarcinoma type 2 diabetes mellitus vaginitis viral meningitis vulvitis vulvovaginitis
2589	polypeptide N-acetylgalactosaminyltransferase 1	GALNT1 Aliases: GalNAc-T1 polypeptide GalNAc transferase 1 protein-UDP acetylgalactosaminyltransferase 1	Homo sapiens (human)	colorectal cancer colorectal carcinoma congenital heart disease congestive heart failure heart valve disease hepatocellular carcinoma large intestine cancer liver cancer ovarian cancer ovarian carcinoma pulmonary valve stenosis stomach cancer stomach carcinoma
2590	polypeptide N-acetylgalactosaminyltransferase 2	GALNT2 Aliases: GalNAc-T2 polypeptide GalNAc transferase 2	Homo sapiens (human)	Crohn's colitis Crohn's disease abdominal obesity-metabolic syndrome 1 achondroplasia acute myeloid leukemia arteriosclerotic cardiovascular disease atherosclerosis cancer central nervous system cancer cerebral infarction cerebrovascular disease cholesterol-ester transfer protein deficiency chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma congenital disorder of glycosylation type II coronary artery disease diabetes mellitus embryoma essential hypertension familial hyperlipidemia gastric adenocarcinoma gliosarcoma hepatocellular carcinoma high grade glioma hyperalphalipoproteinemia 1 hyperglycemia hypertension hypochondroplasia inflammatory bowel disease 1 inflammatory bowel disease liver cancer mixed glioma nutmeg liver obesity papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia squamous cell carcinoma stomach cancer stomach carcinoma temporal arteritis tongue squamous cell carcinoma type 2 diabetes mellitus ulcerative colitis
2591	polypeptide N-acetylgalactosaminyltransferase 3	GALNT3 Aliases: GalNAc-T3 HFTC HHS polypeptide GalNAc transferase 3	Homo sapiens (human)	CHARGE syndrome X-linked dyskeratosis congenita adenocarcinoma adenoma angioid streaks arteriosclerotic cardiovascular disease atherosclerosis autosomal recessive hypophosphatemic rickets bronchus cancer bronchus carcinoma calcinosis calcium metabolism disease cancer carcinoma cerebral infarction cerebrovascular disease chondrocalcinosis chromophobe renal cell carcinoma chronic kidney disease clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma coronary artery disease cribriform carcinoma dental enamel hypoplasia dental pulp calcification dentin dysplasia diabetes mellitus diabetic ketoacidosis disease of metabolism dyskeratosis congenita embryoma endometriosis of uterus endometriosis gallbladder cancer gallbladder carcinoma granular cell carcinoma hypercalcemia hyperostosis hyperphosphatemia hyperphosphatemic familial tumoral calcinosis hypotrichosis 1 hypotrichosis large intestine cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma melanoma microphthalmia musculoskeletal system disease nephrocalcinosis nodular prostate nutmeg liver obsolete Matthew-Wood syndrome obsolete type 1 diabetes mellitus 9 osteoarthritis osteoporosis ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma phosphorus metabolism disease prostate cancer prostate carcinoma prostatic adenoma pulp degeneration renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma skin disease skin melanoma squamous cell carcinoma tongue squamous cell carcinoma 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 viral infectious disease
2592	galactose-1-phosphate uridylyltransferase	GALT	Homo sapiens (human)	acquired immunodeficiency syndrome agnosia androgen insensitivity syndrome bacterial sepsis blood coagulation disease cancer cataract cerebellar ataxia cerebellar disease classic galactosemia cystinuria diabetic cataract diarrhea disease of metabolism endometriosis of uterus endometriosis galactokinase deficiency galactose epimerase deficiency galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hemolytic anemia hepatocellular carcinoma human immunodeficiency virus infectious disease hypoglycemia hypogonadism inherited metabolic disorder intellectual disability kwashiorkor lactic acidosis learning disability liver cancer liver cirrhosis liver disease marasmus neonatal jaundice nutrition disease osteoporosis ovarian cancer ovarian carcinoma premature menopause primary ovarian insufficiency protein-energy malnutrition proteinuria speech-language disorder-1 trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
2595	glucosidase alpha, neutral C	GANC	Homo sapiens (human)	congenital dyserythropoietic anemia panic disorder
2597	glyceraldehyde-3-phosphate dehydrogenase	GAPDH	Homo sapiens (human)	ACTH-secreting pituitary adenoma 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 Burkitt lymphoma Cockayne syndrome Cornelia de Lange syndrome Crohn's colitis Crohn's disease Down syndrome Dubowitz syndrome Ewing sarcoma HELLP 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 IgA glomerulonephritis Japanese encephalitis Kawasaki disease Kennedy's disease Keshan disease Laron syndrome 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 Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Prader-Willi syndrome Reye syndrome Robinow syndrome Seckel syndrome Sertoli cell-only syndrome Silver-Russell syndrome Turner syndrome X-linked Aarskog syndrome X-linked spermatogenic failure 1 Zika fever achondroplasia acidophil adenoma acoustic neuroma acute lymphoblastic leukemia acute megakaryocytic leukemia acute poststreptococcal glomerulonephritis adenosarcoma adrenal adenoma adrenal cortex cancer alcohol dependence alcohol use disorder alcoholic cardiomyopathy alcoholic hepatitis allergic asthma amyloidosis amyotrophic lateral sclerosis angioimmunoblastic T-cell lymphoma angiomatous meningioma aortic aneurysm aortic valve disease 1 aortic valve disease 2 aortic valve stenosis arthritis arthropathy asthma autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome bacterial sepsis basal cell carcinoma benign meningioma bicuspid aortic valve disease bladder carcinoma bone osteosarcoma brain glioma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy central nervous system cancer cerebral convexity meningioma cerebral degeneration cervical cancer cervix carcinoma childhood osteosarcoma chondrodysplasia-pseudohermaphroditism syndrome chromophobe renal cell carcinoma chronic fatigue syndrome clear cell meningioma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease dengue disease dentatorubral-pallidoluysian atrophy developmental and epileptic encephalopathy 2 diabetes mellitus diabetic cataract diabetic retinopathy diffuse large B-cell lymphoma dysplastic nevus syndrome early infantile epileptic encephalopathy embryoma encephalitis encephalomyelitis endocrine exophthalmos endomyocardial fibrosis epilepsy esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma familial hypertrophic cardiomyopathy fasciitis fibrous meningioma follicular lymphoma ganglioneuroblastoma giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis gonadal dysgenesis granuloma annulare hepatitis B hepatitis C hepatitis D hepatocellular carcinoma hereditary spherocytosis high grade glioma hypertrophic cardiomyopathy hypopharynx cancer immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intestinal schistosomiasis intraorbital meningioma intraventricular meningioma intrinsic asthma kidney disease large intestine cancer laryngeal benign neoplasm laryngeal carcinoma larynx cancer late onset Parkinson's disease leishmaniasis liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphangioleiomyomatosis malaria melanoma membranous glomerulonephritis meningioma meningothelial meningioma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcystic meningioma microphthalmia middle cerebral artery infarction mixed glioma multiple endocrine neoplasia type 1 multiple myeloma multiple sclerosis myelitis nephritis nephroblastoma neuroblastoma neurodegenerative disease neuroectodermal tumor nonpapillary renal cell carcinoma obesity obsolete Matthew-Wood syndrome obsolete infantile epileptic encephalopathy obsolete ymphosarcoma olfactory groove meningioma oral squamous cell carcinoma osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma pancreatic adenocarcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma parapsoriasis parasagittal meningioma pituitary adenoma placental insufficiency pre-eclampsia progressive muscular atrophy progressive myoclonus epilepsy prolactinoma prostate cancer prostate carcinoma psammomatous meningioma psoriasis pustulosis of palm and sole reflex sympathetic dystrophy renal carcinoma renal cell carcinoma rheumatic heart disease sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia secretory meningioma sickle cell anemia skin melanoma sleeping sickness spinal meningioma spinal muscular atrophy status epilepticus stomach cancer stomach carcinoma tarsal-carpal coalition syndrome thymic carcinoma thymoma thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma transitional meningioma trypanosomiasis tuberculosis type 2 diabetes mellitus ulcerative colitis urinary bladder cancer viral infectious disease visceral leishmaniasis yellow fever
2619	growth arrest specific 1	GAS1	Homo sapiens (human)	Baraitser-Winter syndrome Fraser syndrome Goldenhar syndrome Kallmann syndrome Laron syndrome Marfan syndrome Moebius syndrome Muenke Syndrome Nance-Horan syndrome Potter's syndrome Sakati-Nyhan syndrome Sheehan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome achondroplasia allergic asthma asthma bilateral renal aplasia bladder carcinoma bone osteosarcoma branchiootic syndrome breast cancer breast carcinoma cancer cavernous hemangioma central nervous system cancer childhood osteosarcoma choanal atresia chorioangioma chromophobe renal cell carcinoma clear cell renal cell carcinoma cleft palate collecting duct carcinoma coloboma colorectal cancer colorectal carcinoma congenital hypothyroidism degenerative disc disease diabetes mellitus diabetic ketoacidosis disorder of sexual development duodenal atresia embryoma epilepsy gestational diabetes giant cell glioblastoma glioblastoma gliosarcoma glomerulonephritis glomus tumor hemangioma hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 1A hereditary sensory neuropathy hermaphroditism high grade glioma histiocytoid hemangioma holoprosencephaly 1 holoprosencephaly hypertropia hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism hypothyroidism intellectual disability intramuscular hemangioma intrinsic asthma isolated cleft palate isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency kidney disease large intestine cancer learning disability lymphangioma mechanical strabismus melanoma microcephaly mixed glioma myxedema nephritis nephrosis neuroblastoma neuropathy nevoid basal cell carcinoma syndrome nonpapillary renal cell carcinoma ophthalmoplegia orofaciodigital syndrome I orofaciodigital syndrome X osteosarcoma panhypopituitarism papillary adenocarcinoma papillary renal cell carcinoma peripheral nervous system disease placental insufficiency primary open angle glaucoma pseudohermaphroditism pyoureter rabies renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma scoliosis sensorineural hearing loss sensory peripheral neuropathy situs inversus skin melanoma solitary median maxillary central incisor stomach cancer stomach carcinoma strabismus tetralogy of Fallot thymus gland disease thyroid gland papillary carcinoma tuberous sclerosis type 2 diabetes mellitus urinary bladder cancer visual epilepsy
2629	glucosylceramidase beta 1	GBA1 Aliases: glucocerebrosidase	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 Burkitt lymphoma Canavan 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 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 Cogan syndrome DiGeorge syndrome Fabry disease 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 Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Lafora disease Langerhans-cell histiocytosis Laron syndrome Lewy body dementia Netherton syndrome Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease type C1 Niemann-Pick disease type C2 Niemann-Pick disease PCWH syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 2 Parkinson's disease 4 Parkinson's disease Parkinsonism Pick's disease REM sleep behavior disorder Reye syndrome Sjogren-Larsson syndrome Tay-Sachs disease Unverricht-Lundborg syndrome West Nile fever Wolman disease abdominal obesity-metabolic syndrome 1 achondroplasia acquired hyperkeratosis actinic keratosis adult lymphoma agenesis of the corpus callosum with peripheral neuropathy agnosia alternating hemiplegia of childhood amyotrophic lateral sclerosis anemia arthritis arthropathy atypical Gaucher's disease due to saposin c deficiency autonomic neuropathy autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis autosomal recessive osteopetrosis 7 blepharospasm brain disease cancer cardiac arrest central nervous system disease central nervous system lymphoma cerebral degeneration childhood lymphoma chylomicron retention disease communicating hydrocephalus congestive heart failure dementia dentatorubral-pallidoluysian atrophy depressive disorder developmental coordination disorder diffuse interstitial keratitis diffuse large B-cell lymphoma dissociated nystagmus dysthymic disorder dystonia early myoclonic encephalopathy ectropion embryoma endometriosis of uterus endometriosis esotropia essential hypertension essential tremor female stress incontinence fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome focal hand dystonia follicular lymphoma glucose intolerance hemopericardium hepatitis B hepatopulmonary syndrome hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 2 hydrocephalus hypertension hypomyelinating leukodystrophy 2 hypomyelinating leukodystrophy 3 hypomyelinating leukodystrophy 4 hypomyelinating leukodystrophy 6 hypomyelinating leukodystrophy 9 ichthyosis interstitial lung disease intracranial aneurysm keratosis follicularis late onset Parkinson's disease leukoencephalopathy with vanishing white matter leukopenia lingual-facial-buccal dyskinesia lipid storage disease liver cirrhosis lymphoma lysosomal storage disease macrocytic anemia major depressive disorder melancholic depression metachromatic leukodystrophy microcephaly mitral valve stenosis mongolian spot monocular esotropia motor peripheral neuropathy movement disease multiple myeloma nervous system disease neuroblastoma neurodegenerative disease neurotic disorder non-Hodgkin lymphoma obsolete congenital ichthyosiform erythroderma obsolete constipation obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obsolete ymphosarcoma obstructive hydrocephalus ophthalmoplegia osteoarthritis osteonecrosis osteopetrosis osteosclerosis pancytopenia pathologic nystagmus pericardial effusion placental insufficiency polyhydramnios prediabetes syndrome primary pulmonary hypertension progressive muscular atrophy progressive myoclonus epilepsy 4 progressive myoclonus epilepsy progressive supranuclear palsy proteinuria pseudoxanthoma elasticum psoriasis reticulosarcoma schizophrenia seborrheic keratosis secondary Parkinson disease senile degeneration of brain sensorineural hearing loss skin disease speech disorder sphingolipidosis spontaneous ocular nystagmus thrombocytopenia velocardiofacial syndrome
2632	1,4-alpha-glucan branching enzyme 1	GBE1 Aliases: Andersen disease glycogen branching enzyme glycogen storage disease type IV	Homo sapiens (human)	B-cell lymphoma Cauda equina syndrome Fabry disease Gerstmann-Straussler-Scheinker syndrome Gorham's disease Guillain-Barre syndrome Noonan syndrome 1 acute myeloid leukemia bronchus cancer bronchus carcinoma cancer cardiomyopathy carnitine palmitoyltransferase II deficiency cerebral infarction cerebrovascular disease chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy chronic ulcer of skin chylomicron retention disease congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A congestive heart failure contractures, pterygia, and spondylocarpotarsal fusion syndrome cystinuria cytochrome-c oxidase deficiency disease dementia diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy 1A dilated cardiomyopathy disease of metabolism embryoma endomyocardial fibrosis esophagus squamous cell carcinoma familial lipoprotein lipase deficiency familial periodic paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome galactosemia gallbladder disease glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease III glycogen storage disease IV glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease VI glycogen storage disease VII glycogen storage disease hypertrophic cardiomyopathy idiopathic scoliosis intellectual disability learning disability leukodystrophy lipid storage disease liver disease locked-in syndrome lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma megaconial type congenital muscular dystrophy melanoma mitochondrial metabolism disease mitochondrial myopathy mitochondrial trifunctional protein deficiency multiple sclerosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myopathy nemaline myopathy neurogenic bladder obsolete ymphosarcoma ovarian cancer ovarian carcinoma paraplegia polyhydramnios porphyria portal hypertension pulmonary tuberculosis quadriplegia rigid spine muscular dystrophy 1 skin melanoma
2639	glutaryl-CoA dehydrogenase	GCDH Aliases: ACAD5 GCD	Homo sapiens (human)	D-2-hydroxyglutaric aciduria 1 D-2-hydroxyglutaric aciduria Fleck corneal dystrophy alternating hemiplegia of childhood autonomic neuropathy basal ganglia disease blepharospasm brain disease brain ischemia central nervous system disease central nervous system origin vertigo cerebral palsy colorectal cancer colorectal carcinoma corneal dystrophy disease of metabolism dystonia epilepsy focal hand dystonia generalized dystonia glutaric acidemia I granular corneal dystrophy 2 hemiplegia hyperlysinemia hypoglycemia inherited metabolic disorder lactic acidosis large intestine cancer lattice corneal dystrophy lingual-facial-buccal dyskinesia liver cirrhosis malignant hyperthermia migraine movement disease nervous system disease oligohydramnios spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy speech disorder transient cerebral ischemia visual epilepsy
2641	glucagon	GCG	Homo sapiens (human)	Alzheimer's disease prediabetes syndrome
2645	glucokinase	GCK Aliases: HK4 hexokinase 4	Homo sapiens (human)	Chagas disease Fanconi anemia complementation group C Fanconi anemia Laron syndrome Marfan syndrome Werner syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 achondroplasia acute chest syndrome adult-onset Still's disease agnosia apraxia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis autoimmune disease autoimmune lymphoproliferative syndrome bronchus cancer bronchus carcinoma cancer cardiovascular system disease chronic fatigue syndrome congenital heart disease congenital ptosis coronary artery disease diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic retinopathy disease of metabolism embryoma encephalitis encephalomyelitis endocrine pancreas disease epilepsy essential hypertension familial adenomatous polyposis 1 familial adenomatous polyposis familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 familial hyperinsulinemic hypoglycemia 3 generalized anxiety disorder gestational diabetes glomerulonephritis glucose intolerance glucose metabolism disease heart disease hepatocellular carcinoma hyperglycemia hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypoglycemia hypoglycemic coma immune system disease insulinoma intellectual disability kidney disease learning disability leishmaniasis liver cancer liver carcinoma liver cirrhosis lung benign neoplasm lung cancer lung carcinoma maturity-onset diabetes of the young type 2 maturity-onset diabetes of the young type 3 maturity-onset diabetes of the young myelitis myotonic dystrophy type 1 myotonic dystrophy type 2 neonatal diabetes nephritis nephrosis neuropathy nutmeg liver obesity obsolete infantile epileptic encephalopathy obsolete type 1 diabetes mellitus 9 osteoarthritis pancreatic cancer pancreatic carcinoma peripheral nervous system disease permanent neonatal diabetes mellitus placental insufficiency polyneuropathy prediabetes syndrome progeria prostate cancer prostate carcinoma ptosis pyoureter retinal disease retinitis rheumatoid arthritis sensorineural hearing loss situs inversus steatotic liver disease syndromic X-linked intellectual disability 94 systemic lupus erythematosus transient neonatal diabetes mellitus trypanosomiasis 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 urea cycle disorder visceral leishmaniasis visual epilepsy
2648	lysine acetyltransferase 2A	KAT2A	Homo sapiens (human)	heart disease kidney disease lung non-small cell carcinoma
2650	glucosaminyl (N-acetyl) transferase 1	GCNT1 Aliases: C2GNT NAGCT2 beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N--acetylglucosaminyltransferase core 2 beta1,6 N-acetylglucosaminyltransferase-I	Homo sapiens (human)	adenocarcinoma adenoma bronchus cancer bronchus carcinoma cancer carcinoma colorectal cancer colorectal carcinoma cribriform carcinoma embryoma granular cell carcinoma large intestine cancer lung benign neoplasm lung cancer lung carcinoma neuroblastoma pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma sarcomatoid carcinoma seminoma testicular cancer testicular germ cell cancer tubular adenocarcinoma
2651	glucosaminyl (N-acetyl) transferase 2 (I blood group)	GCNT2 Aliases: IGNT Ii blood group NAGCT1 ULG3 bA360O19.2 bA421M1.1 unassigned linkage group 3	Homo sapiens (human)	abdominal obesity-metabolic syndrome 1 breast cancer breast carcinoma cancer cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cervical adenocarcinoma cervical cancer cervix carcinoma childhood acute lymphocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma esophagus squamous cell carcinoma gallbladder cancer gallbladder carcinoma hyperferritinemia-cataract syndrome kidney failure large intestine cancer melanoma skin melanoma tuberculosis uremia
2653	glycine cleavage system protein H	GCSH Aliases: lipoic acid-containing protein	Homo sapiens (human)	Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome 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 Seckel syndrome Silver-Russell syndrome Unverricht-Lundborg syndrome X-linked Aarskog syndrome amino acid metabolic disorder autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome blepharospasm brain disease breast cancer breast carcinoma cancer central nervous system lymphoma chondrodysplasia-pseudohermaphroditism syndrome early myoclonic encephalopathy embryoma epilepsy focal hand dystonia glycine encephalopathy intellectual disability learning disability lymphoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II multiple mitochondrial dysfunctions syndrome obsolete ymphosarcoma schizophrenia urea cycle disorder visual epilepsy
2673	glutamine--fructose-6-phosphate transaminase 1	GFPT1 Aliases: GFA GFAT GFAT1	Homo sapiens (human)	Bell's palsy Laron syndrome Machado-Joseph disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Zollinger-Ellison syndrome achondroplasia agnosia brain cancer breast cancer breast carcinoma cancer centronuclear myopathy clubfoot congenital myasthenic syndrome 12 congenital myasthenic syndrome 4C congenital myasthenic syndrome congenital ptosis congenital structural myopathy developmental coordination disorder diabetes mellitus diabetic ketoacidosis embryoma facial nerve disease facial paralysis familial hyperlipidemia familial periodic paralysis giant cell glioblastoma glioblastoma glomerulonephritis hepatitis B hepatocellular carcinoma high grade glioma hyperglycemia hyperinsulinism hypertropia isolated elevated serum creatine phosphokinase levels kidney disease liver cancer mechanical strabismus myopathy nasopharynx carcinoma nephritis nephrosis neuromuscular disease neuromuscular junction disease obesity ophthalmoplegia pancreatic cancer pancreatic carcinoma ptosis pyoureter scoliosis stomach cancer stomach carcinoma strabismus tubular aggregate myopathy 1 type 2 diabetes mellitus
2674	GDNF family receptor alpha 1	GFRA1 Aliases: GDNFR GFR-ALPHA-1 RET1L RETL1 TRNR1	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 Churg-Strauss syndrome Hirschsprung's disease Kennedy's disease Parkinsonism Pick's disease Reye syndrome acute promyelocytic leukemia adult cystic teratoma adult teratoma amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease autosomal recessive distal hereditary motor neuronopathy 1 bone osteosarcoma brain cancer brain ischemia breast cancer breast carcinoma breast fibrocystic disease cancer cerebral degeneration cerebral infarction cerebrovascular disease childhood osteosarcoma colorectal cancer colorectal carcinoma cystic teratoma embryoma embryonal cancer endemic goiter germ cell and embryonal cancer germ cell cancer hepatitis C hepatocellular carcinoma idiopathic scoliosis large intestine cancer lateral sclerosis lesion of sciatic nerve liver cancer malignant teratoma mature teratoma melanoma microglandular adenosis migraine without aura motor neuron disease neuroendocrine carcinoma neuroendocrine tumor neuropathy obsolete ymphosarcoma osteosarcoma pancreatic cancer pancreatic carcinoma peripheral nervous system disease polyarteritis nodosa polyneuropathy preretinal fibrosis progressive muscular atrophy prostate cancer prostate carcinoma renal agenesis rheumatoid arthritis schizophrenia sciatic neuropathy secondary Parkinson disease skin melanoma substernal goiter teratoma thrombophilia thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland medullary carcinoma vascular dementia vesicoureteral reflux
2675	GDNF family receptor alpha 2	GFRA2 Aliases: GDNFRB NTNRA RETL2 TRNR2	Homo sapiens (human)	Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Hirschsprung's disease Parkinsonism adenocarcinoma adenoma bipolar disorder cancer colorectal cancer colorectal carcinoma follicular adenoma frontotemporal dementia hepatocellular carcinoma large intestine cancer lingual-facial-buccal dyskinesia liver cancer microcystic adenoma neuroblastoma neuropathy pancreatic cancer pancreatic carcinoma papillary adenoma peripheral nervous system disease polyneuropathy preretinal fibrosis schizophrenia secondary Parkinson disease
2678	gamma-glutamyltransferase 1	GGT1	Homo sapiens (human)	ARC syndrome Aicardi-Goutieres syndrome Alagille 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 3 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Leber hereditary optic neuropathy Pick's disease Potter's syndrome Reye syndrome Werner syndrome abdominal obesity-metabolic syndrome 1 acute lymphoblastic leukemia acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adrenoleukodystrophy adult acute lymphocytic leukemia aflatoxins-related hepatocellular carcinoma alcohol dependence alcohol use disorder alcoholic liver cirrhosis allergic asthma ameloblastoma anthracosilicosis anthracosis arteriosclerotic cardiovascular disease arthritis arthrogryposis, renal dysfunction, and cholestasis 1 arthropathy asbestosis asthma atherosclerosis atrial fibrillation benign recurrent intrahepatic cholestasis bile duct adenocarcinoma bile duct carcinoma biliary atresia breast apocrine carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiovascular system disease central nervous system lymphoma cerebral degeneration cerebral infarction cerebrovascular disease childhood acute lymphocytic leukemia cholangiocarcinoma cholecystitis cholestasis chromophobe renal cell carcinoma chronic kidney disease citrullinemia clear cell renal cell carcinoma collecting duct carcinoma colorectal cancer colorectal carcinoma common wart coronary artery disease coronary stenosis coronary thrombosis cribriform carcinoma diabetes mellitus diabetic cataract diabetic ketoacidosis diabetic neuropathy diabetic retinopathy differentiated thyroid gland carcinoma distal arthrogryposis embryoma endometrial cancer endometrial carcinoma epithelioid leiomyosarcoma essential hypertension essential thrombocythemia exfoliation syndrome familial hyperlipidemia gallbladder cancer gallbladder carcinoma gallbladder disease gamma-glutamyl transpeptidase deficiency gelatinous drop-like corneal dystrophy gestational diabetes gestational trophoblastic neoplasm glucose intolerance glycogen storage disease VIII granular cell carcinoma head and neck cancer head and neck squamous cell carcinoma heart disease hepatitis B hepatitis C hepatitis hepatocellular carcinoma hyperglycemia hypertension idiopathic interstitial pneumonia idiopathic pulmonary fibrosis ileus inflammatory bowel disease inflammatory liposarcoma influenza intellectual disability interstitial lung disease intestinal obstruction intrahepatic cholangiocarcinoma intrahepatic cholestasis intrinsic asthma kidney failure large intestine cancer learning disability leiomyosarcoma leukemia liver cancer liver carcinoma liver cirrhosis liver disease lung benign neoplasm lung cancer lung carcinoma lymphoma maturity-onset diabetes of the young melanoma mitochondrial metabolism disease mitochondrial myopathy morbid obesity myelodysplastic syndrome myocardial infarction myxoid leiomyosarcoma nasopharynx carcinoma neonatal jaundice nodular prostate non-alcoholic fatty liver nonpapillary renal cell carcinoma nontoxic goiter nutmeg liver obesity obsolete dyspepsia obsolete ymphosarcoma osteoarthritis osteomalacia ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary adenocarcinoma papillary renal cell carcinoma peptic ulcer disease periodontitis polycystic ovary syndrome prediabetes syndrome primary biliary cholangitis progeria progressive familial intrahepatic cholestasis 1 progressive familial intrahepatic cholestasis progressive supranuclear palsy prostate cancer prostate carcinoma prostatic adenoma renal carcinoma renal cell carcinoma rickets sarcomatoid carcinoma sarcomatoid renal cell carcinoma sclerosing liposarcoma seminoma silent myocardial infarction skin benign neoplasm skin cancer skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma tauopathy testicular cancer testicular germ cell cancer testis seminoma thrombocytopenia thyroid gland papillary carcinoma tongue squamous cell carcinoma tubular adenocarcinoma type 2 diabetes mellitus uremia uterine corpus cancer viral infectious disease well-differentiated liposarcoma
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

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