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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 **726 - 750** of **1582** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
5208	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	PFKFB2	Homo sapiens (human)	bone osteosarcoma breast cancer cancer childhood acute lymphocytic leukemia diabetes mellitus embryoma giant cell glioblastoma glioblastoma high grade glioma melanoma osteosarcoma placental insufficiency skin melanoma stomach cancer type 2 diabetes mellitus
10007	glucosamine-6-phosphate deaminase 1	GNPDA1 Aliases: GNPDA GPI HLN KIAA0060 glucosamine-6-phosphate deaminase oscillin	Homo sapiens (human)
79611	acyl-CoA synthetase short chain family member 3	ACSS3 Aliases: FLJ21963	Homo sapiens (human)	cancer embryoma stomach cancer stomach carcinoma
8693	polypeptide N-acetylgalactosaminyltransferase 4	GALNT4 Aliases: GalNAc-T4 polypeptide GalNAc transferase 4	Homo sapiens (human)	acute chest syndrome arteriosclerotic cardiovascular disease atherosclerosis breast cancer cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease large intestine cancer prostate cancer prostate carcinoma
79071	ELOVL fatty acid elongase 6	ELOVL6 Aliases: FLJ23378 LCE MGC5487	Homo sapiens (human)	Fanconi anemia complementation group A Fanconi anemia Zollinger-Ellison syndrome accommodative esotropia acrodermatitis acute myeloid leukemia acute myocardial infarction allergic contact dermatitis amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis azoospermia bronchus cancer bronchus carcinoma cancer cone-rod dystrophy congestive heart failure coronary artery disease coronary thrombosis dermatitis diabetes mellitus disease of metabolism dissociative amnesia fundus albipunctatus hepatocellular carcinoma hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma myocardial infarction nodular prostate obesity parapsoriasis postinflammatory pulmonary fibrosis prostatic adenoma psoriasis psoriatic arthritis pulmonary fibrosis pustulosis of palm and sole retinitis pigmentosa silent myocardial infarction steatotic liver disease type 2 diabetes mellitus
2822	glycosylphosphatidylinositol specific phospholipase D1	GPLD1	Homo sapiens (human)	Budd-Chiari syndrome Norum disease Richter's syndrome Tangier disease abetalipoproteinemia acute myocardial infarction arteriosclerotic cardiovascular disease atherosclerosis brain infarction breast cancer breast carcinoma cancer carcinoma choreaacanthocytosis chronic lymphocytic leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease coronary thrombosis embryoma hypolipoproteinemia large intestine cancer melanoma myocardial infarction nutmeg liver osteoporosis papillary carcinoma prostate cancer prostate carcinoma rheumatoid arthritis sarcomatoid carcinoma silent myocardial infarction skin melanoma succinic semialdehyde dehydrogenase deficiency thyroid adenoma thyroid cancer thyroid gland carcinoma
3990	lipase C, hepatic type	LIPC Aliases: HL HTGL Triacylglycerol lipase	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 Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Kuhnt-Junius degeneration Pick's disease Reye syndrome Zollinger-Ellison syndrome abdominal obesity-metabolic syndrome 1 acute myocardial infarction age related macular degeneration arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation bacterial sepsis cancer cardiovascular system disease carotid artery disease carotid artery thrombosis carotid stenosis cerebral degeneration cerebral infarction cerebrovascular disease cholesterol-ester transfer protein deficiency chronic kidney disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital hypothyroidism congestive heart failure coronary artery disease coronary thrombosis degeneration of macula and posterior pole diabetes mellitus diabetic ketoacidosis embryoma end stage renal disease endometriosis of uterus endometriosis essential hypertension familial combined hyperlipidemia familial hypercholesterolemia familial hyperlipidemia familial nephrotic syndrome focal segmental glomerulosclerosis glomerulonephritis glucose intolerance glycogen storage disease II heart disease hepatitis hyperalphalipoproteinemia 1 hyperinsulinism hypertension hypothyroidism idiopathic scoliosis intermittent claudication ischemia kidney disease large intestine cancer lipid metabolism disorder lipoid nephrosis lung cancer lung non-small cell carcinoma macroglobulinemia macular degeneration marasmus myocardial infarction myxedema nephritis nephrosis nephrotic syndrome neurodegenerative disease nutmeg liver obesity obsolete lymphoplasmacytic lymphoma obsolete type 1 diabetes mellitus 9 peripheral artery disease peripheral vascular disease pre-eclampsia prediabetes syndrome protein-energy malnutrition pyoureter schizophrenia silent myocardial infarction 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 vascular disease
6514	solute carrier family 2 member 2	SLC2A2 Aliases: GLUT-2	Homo sapiens (human)	B-cell lymphoma Fanconi syndrome Laron syndrome X-linked dominant hypophosphatemic rickets abdominal obesity-metabolic syndrome 1 achondroplasia atopic dermatitis breast cancer breast carcinoma cancer carcinoma cardiovascular system disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cystinosis cystinuria dental caries dentin caries dermatitis diabetes mellitus diabetic ketoacidosis disease of metabolism embryoma essential hypertension familial adenomatous polyposis galactokinase deficiency galactosemia gastrinoma gestational diabetes glomerulonephritis glucose intolerance glucose metabolism disease glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease heart disease hepatitis C hepatocellular carcinoma hyperglycemia hypertension hypoglycemia hypokalemia hypophosphatemia insulinoma intestinal atresia islet cell tumor kidney disease kidney failure lactic acidosis large intestine cancer liver cancer lung squamous cell carcinoma maturity-onset diabetes of the young melanoma myelomeningocele neonatal diabetes nephritis nephrosis obesity obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma osteomalacia oxyphilic adenoma papillary renal cell carcinoma permanent neonatal diabetes mellitus placental insufficiency prediabetes syndrome pyoureter renal carcinoma renal cell carcinoma renal glycosuria renal oncocytoma rickets sarcomatoid carcinoma sarcomatoid renal cell carcinoma skin melanoma spondyloepimetaphyseal dysplasia, Sponastrime type squamous cell carcinoma steatotic liver disease tethered spinal cord syndrome tongue squamous cell carcinoma transient neonatal diabetes mellitus tropical sprue 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
54490	UDP glucuronosyltransferase family 2 member B28	UGT2B28	Homo sapiens (human)	Addison's disease adrenal cortical hypofunction cancer colorectal cancer colorectal carcinoma hepatocellular carcinoma large intestine cancer liver cancer primary cutaneous amyloidosis prostate cancer prostate carcinoma
221	aldehyde dehydrogenase 3 family member B1	ALDH3B1 Aliases: aldehyde dehydrogenase 3B1 aldehyde dehydrogenase 7	Homo sapiens (human)	Sjogren-Larsson syndrome chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma delusional disorder papillary renal cell carcinoma paranoid schizophrenia renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia
224	aldehyde dehydrogenase 3 family member A2	ALDH3A2 Aliases: FALDH fatty aldehyde dehydrogenase	Homo sapiens (human)	Cogan syndrome Laron syndrome Senior-Loken syndrome Sjogren-Larsson syndrome X-linked adrenal hypoplasia congenita achondroplasia acquired hyperkeratosis acrodermatitis age related macular degeneration allergic asthma alternating hemiplegia of childhood angioedema asthma 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 central nervous system disease cerebral palsy cone-rod dystrophy corneal disease degeneration of macula and posterior pole dental enamel hypoplasia dermatitis diabetic ketoacidosis epilepsy ethylmalonic encephalopathy fundus albipunctatus granuloma annulare hepatitis B ichthyosis intellectual disability intrinsic asthma keratoconus keratosis follicularis learning disability lipid metabolism disorder localized scleroderma locked-in syndrome lung cancer lung non-small cell carcinoma macular degeneration microcephaly mongolian spot mucopolysaccharidosis IV multiple epiphyseal dysplasia myopia nephronophthisis nervous system disease normal pressure hydrocephalus obsolete asthenopia obsolete congenital ichthyosiform erythroderma obsolete type 1 diabetes mellitus 9 osteochondrodysplasia papilloma paraplegia pseudoxanthoma elasticum quadriplegia retinal disease retinitis pigmentosa retinitis scleroderma scoliosis spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy squamous cell papilloma squamous papillomatosis systemic scleroderma 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 urticaria visual epilepsy
221927	BRCA1 associated ATM activator 1	BRAT1	Homo sapiens (human)
1431	citrate synthase	CS	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 Brill-Zinsser disease Graves' disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Pick's disease Poland syndrome Q fever Reye syndrome Sengers syndrome Siberian tick typhus Zollinger-Ellison syndrome adrenal gland cancer amyotrophic lateral sclerosis anaplastic astrocytoma autism spectrum disorder autistic disorder bacillary angiomatosis bacterial sepsis bipolar disorder cancer cardiomyopathy carnitine palmitoyltransferase II deficiency cerebral degeneration childhood cerebral astrocytoma chronic obstructive pulmonary disease congestive heart failure coronary artery disease depressive disorder dermoid cyst of ovary diabetes mellitus diabetic ketoacidosis dilated cardiomyopathy duodenum cancer dysthymic disorder embryoma endocarditis endomyocardial fibrosis fibrillary astrocytoma gangliocytoma ganglioneuroma gemistocytic astrocytoma giant cell glioblastoma glioblastoma heart cancer high grade glioma hyperinsulinism hyperthyroidism hypertrophic cardiomyopathy hypothyroidism juvenile pilocytic astrocytoma limb ischemia major depressive disorder malaria malignant astrocytoma melancholic depression mitochondrial DNA depletion syndrome 12b mitochondrial DNA depletion syndrome mitochondrial metabolism disease mitochondrial myopathy myocardial infarction myofibrillar myopathy neuroblastoma neurotic disorder obesity obsolete melancholia obsolete ymphosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma parapsoriasis peripheral artery disease pheochromocytoma pilocytic astrocytoma primary pulmonary hypertension progressive muscular atrophy protoplasmic astrocytoma psoriasis pustulosis of palm and sole retinal degeneration rickettsialpox small intestine cancer spondylocarpotarsal synostosis syndrome spotted fever steatotic liver disease subependymal giant cell astrocytoma thyrotoxicosis trypanosomiasis type 2 diabetes mellitus typhus
10394	proteoglycan 3, pro eosinophil major basic protein 2	PRG3 Aliases: MBP2 MBPH	Homo sapiens (human)	brain cancer cancer cerebral infarction cerebrovascular disease embryoma
3706	inositol-trisphosphate 3-kinase A	ITPKA Aliases: IP3-3KA IP3KA	Homo sapiens (human)	allergic asthma asthma bronchus cancer bronchus carcinoma cancer central nervous system cancer embryoma gliosarcoma high grade glioma intrinsic asthma lung cancer lung carcinoma mixed glioma
56052	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	ALG1 Aliases: CDG1K HMAT1 HMT-1 Mat-1	Homo sapiens (human)	B-cell lymphoma Cauda equina syndrome Creutzfeldt-Jakob disease Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Walker-Warburg syndrome amyotrophic lateral sclerosis type 1 breast cancer breast carcinoma breast fibroadenoma bronchus cancer bronchus carcinoma cancer cardiomyopathy cerebral degeneration cerebral infarction cerebrovascular disease colon cancer colonic benign neoplasm congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A1 diabetes mellitus endomyocardial fibrosis enophthalmos epilepsy familial hypertrophic cardiomyopathy familial nephrotic syndrome focal epilepsy glomerulonephritis goiter hepatocellular carcinoma hyperthyroidism hypertrophic cardiomyopathy hypogonadism kidney disease laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus nephritis lymphoma malignant pleural mesothelioma microcephaly nephritis nephrosis nephrotic syndrome type 1 nephrotic syndrome neurogenic bladder nodular goiter obsolete exophthalmos obsolete ymphosarcoma orbital disease partial motor epilepsy placental insufficiency pyoureter reticulosarcoma schizophrenia scoliosis systemic lupus erythematosus thyroid gland disease thyrotoxicosis type 2 diabetes mellitus urinary tract obstruction visual epilepsy
27230	stress associated endoplasmic reticulum protein 1	SERP1	Homo sapiens (human)
2135	exostosin like glycosyltransferase 2	EXTL2 Aliases: alpha-1,4-N-acteylhexosaminyltransferase	Homo sapiens (human)	autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 cancer chronic kidney disease hereditary multiple exostoses mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIC mucopolysaccharidosis osteopetrosis osteosclerosis
8802	succinate-CoA ligase GDP/ADP-forming subunit alpha	SUCLG1	Homo sapiens (human)	Leigh disease McCune Albright syndrome brain disease cardiomyopathy central nervous system cancer cerebral degeneration endomyocardial fibrosis epilepsy familial hypertrophic cardiomyopathy giant cell glioblastoma glioblastoma gliosarcoma high grade glioma hypertrophic cardiomyopathy hypoglycemia hypophosphatemia intellectual disability lactic acidosis learning disability methylmalonic acidemia mitochondrial DNA depletion syndrome 5 mitochondrial DNA depletion syndrome 9 mitochondrial DNA depletion syndrome mitochondrial encephalomyopathy mixed glioma skin disease stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 visual epilepsy
3418	isocitrate dehydrogenase (NADP(+)) 2	IDH2 Aliases: IDH-2	Homo sapiens (human)	2-hydroxyglutaric aciduria 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 Balo concentric sclerosis Burkitt lymphoma Cenani-Lenz syndactyly syndrome Chediak-Higashi syndrome D-2-hydroxyglutaric aciduria 1 D-2-hydroxyglutaric aciduria 2 D-2-hydroxyglutaric aciduria Duchenne muscular dystrophy Keshan disease Langerhans-cell histiocytosis Laron syndrome Maffucci syndrome Marinesco-Sjogren syndrome Ollier disease Pelger-Huet anomaly Peutz-Jeghers syndrome Pick's disease Reye syndrome Richter's syndrome T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia achondroplasia acoustic neuroma acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute promyelocytic leukemia adenocarcinoma adenoma adrenal cortex cancer adrenal gland cancer adrenoleukodystrophy adult acute lymphocytic leukemia adult astrocytic tumor adult lymphoma adult medulloblastoma adult oligodendroglioma alpha thalassemia-X-linked intellectual disability syndrome anaplastic astrocytoma anemia angioimmunoblastic T-cell lymphoma angiokeratoma aortic valve insufficiency aromatase excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atypical chronic myeloid leukemia, BCR-ABL1 negative autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy benign ependymoma benign mastocytoma bile duct adenocarcinoma bile duct cancer bile duct carcinoma biliary tract cancer bipolar disorder bone cancer bone giant cell tumor bone marrow cancer bone osteosarcoma bone remodeling disease brain cancer brain stem glioma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma cardiomyopathy cardiovascular system disease cavernous hemangioma cellular ependymoma central nervous system cancer central nervous system disease central nervous system lymphoma cerebral degeneration cerebral palsy cherubism childhood acute lymphocytic leukemia childhood acute myeloid leukemia childhood astrocytic tumor childhood cerebral astrocytoma childhood leukemia childhood lymphoma childhood medulloblastoma childhood oligodendroglioma childhood osteosarcoma childhood pilocytic astrocytoma cholangiocarcinoma chondroblastoma chondroma chondrosarcoma chorioangioma chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chronic ulcer of skin colitis colorectal cancer colorectal carcinoma cone-rod dystrophy congenital muscular dystrophy coronary artery disease cranial nerve disease cranial nerve palsy cribriform carcinoma degenerative disc disease demyelinating polyneuropathy diffuse infiltrative lymphocytosis syndrome diffuse large B-cell lymphoma disease of metabolism distal arthrogryposis distal myopathy duodenum cancer embryoma embryonal cancer endomyocardial fibrosis epilepsy epithelioid sarcoma esophagus squamous cell carcinoma essential hypertension essential thrombocythemia exanthem exostosis extracutaneous mastocytoma facioscapulohumeral muscular dystrophy familial hypertrophic cardiomyopathy familial retinoblastoma fibrillary astrocytoma focal epilepsy fundus albipunctatus ganglioglioma gastroenteritis gemistocytic astrocytoma germ cell and embryonal cancer germ cell cancer germinoma giant cell glioblastoma glioblastoma gliosarcoma glomus tumor goiter granular cell carcinoma head and neck squamous cell carcinoma heart cancer heart disease hemangioma hematologic cancer hematopoietic system disease hemiplegia hepatocellular carcinoma hepatocellular clear cell carcinoma hereditary multiple exostoses hidradenitis suppurativa hidradenitis high grade glioma histiocytoid hemangioma hydronephrosis hypertension hypertrophic cardiomyopathy ileitis ileocolitis indolent systemic mastocytosis inflammatory bowel disease inflammatory breast carcinoma inflammatory liposarcoma intellectual disability intrahepatic cholangiocarcinoma intramuscular hemangioma juvenile pilocytic astrocytoma kidney failure large intestine cancer learning disability leukemia limb-girdle muscular dystrophy liver cancer liver carcinoma luminal breast carcinoma A lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung squamous cell carcinoma lymphangioma lymphoblastic lymphoma lymphoid leukemia lymphoma macrocytic anemia malignant astrocytoma malignant fibrous histiocytoma mast cell neoplasm mastocytosis medulloblastoma medullomyoblastoma melanoma melanotic medulloblastoma meningioma mixed glioma mixed oligodendroglioma-astrocytoma mononeuritis multiplex mononeuropathy multiple myeloma muscular dystrophy myelodysplastic syndrome myelofibrosis myeloid leukemia myeloproliferative neoplasm myofibrillar myopathy 1 myofibrillar myopathy 3 myxopapillary ependymoma narcolepsy nervous system disease neurodegenerative disease neuroendocrine carcinoma neurofibromatosis 1 neurofibromatosis neuropathy non-Hodgkin lymphoma nontoxic goiter obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete ymphosarcoma oculopharyngeal muscular dystrophy olfactory neuroblastoma oligodendroglioma osteoarthritis osteoporosis osteosarcoma ovarian cancer ovarian carcinoma papillary carcinoma papillary ependymoma paraganglioma parathyroid adenoma parathyroid carcinoma partial motor epilepsy periarthritis peripheral T-cell lymphoma peripheral nervous system disease pheochromocytoma pilocytic astrocytoma pituitary adenoma pituitary cancer pituitary carcinoma plasmacytoma pleomorphic xanthoastrocytoma polycythemia vera polycythemia polyneuropathy pompholyx primary cerebellar degeneration prostate cancer prostate carcinoma protoplasmic astrocytoma pulmonary large cell neuroendocrine carcinoma reflex sympathetic dystrophy reticulosarcoma retinitis pigmentosa retinoblastoma rippling muscle disease 2 sarcoma sarcomatoid carcinoma sclerosing liposarcoma scoliosis sensorineural hearing loss skin melanoma small intestine cancer spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spindle cell hemangioma spindle cell sarcoma status epilepticus steatotic liver disease stomach cancer stomach carcinoma subependymal giant cell astrocytoma tanycytic ependymoma telangiectatic osteogenic sarcoma tendinitis thrombophilia thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland disease thyroid gland follicular carcinoma transitional cell carcinoma trilateral retinoblastoma tubular adenocarcinoma uremia urticaria pigmentosa visual epilepsy von Hippel-Lindau disease vulvar dystrophy well-differentiated liposarcoma
55862	ethylmalonyl-CoA decarboxylase 1	ECHDC1 Aliases: dJ351K20.2	Homo sapiens (human)	bladder carcinoma breast cancer breast carcinoma melanoma ovarian cancer ovarian carcinoma skin melanoma urinary bladder cancer
10333	toll like receptor 6	TLR6	Homo sapiens (human)	aspergillosis asthma bacterial pneumonia infective endocarditis perinatal necrotizing enterocolitis rhinitis tuberculosis
90161	heparan sulfate 6-O-sulfotransferase 2	HS6ST2 Aliases: HS6ST-2	Homo sapiens (human)	Paganini-Miozzo syndrome arthritis arthropathy idiopathic interstitial pneumonia idiopathic pulmonary fibrosis intellectual disability learning disability lung adenocarcinoma lung cancer myopia osteoarthritis stomach cancer stomach carcinoma
129642	membrane bound O-acyltransferase domain containing 2	MBOAT2 Aliases: FLJ14415 FLJ90298 LPLAT13 Lysophospholipid acyltransferase 2 lysophospholipid acyltransferase 13	Homo sapiens (human)	adrenoleukodystrophy
347527	arylsulfatase family member H	ARSH	Homo sapiens (human)	Marfan syndrome Richter's syndrome X-linked chondrodysplasia punctata 1 acquired immunodeficiency syndrome acrodermatitis alcoholic liver cirrhosis autosomal dominant chondrodysplasia punctata cancer childhood leukemia chondrodysplasia punctata chronic lymphocytic leukemia dermatitis dyschromatosis symmetrica hereditaria essential thrombocythemia gallbladder disease hepatitis human immunodeficiency virus infectious disease leukemia liver cirrhosis liver disease microphthalmia mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis mucosulfatidosis myelodysplastic syndrome neuroblastoma obsolete Matthew-Wood syndrome oculocerebrorenal syndrome rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 situs inversus tuberous sclerosis ventricular septal defect

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