GlyCosmos Portal

Displaying entries **51 - 75** of **186** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
182316	Putative glycosyltransferase C06E1.7	C06E1.7
181790	Ceramide glucosyltransferase 2	cgt-2	hypertension
181778	Alpha,alpha-trehalose-phosphate synthase [UDP-forming] 1	tps-1
181637	Trehalose-phosphatase	gob-1
181517	putative beta-mannosidase	C33G3.4	beta-mannosidosis
181413	Putative UDP-glucuronosyltransferase ugt-50;UDP-glucuronosyltransferase;glucuronosyltransferase	ugt-50
181323	Sphingomyelin phosphodiesterase 2	asm-2	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
181309	Heparan sulfate 2-O-sulfotransferase hst-2	hst-2
181205	UDP-glucuronosyltransferase	ugt-23
181160	Putative alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	gly-13
181007	UDP-Glucose Glycoprotein glucosylTransferase	uggt-1
181005	Alpha-1,3-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	gly-12
180644	Glycogenin-1	gyg-1	glycogen storage disease XV
180628	putative endochitinase	cht-1	acute myeloid leukemia arteriosclerosis asthma bacterial meningitis breast cancer bronchopulmonary dysplasia chondrosarcoma chronic obstructive pulmonary disease colorectal carcinoma congestive heart failure coronary artery disease cryptococcosis 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 silicosis sinusitis small cell carcinoma systemic scleroderma temporal arteritis type 1 diabetes mellitus type 2 diabetes mellitus
180607	GDP-fucose protein O-fucosyltransferase 1	pfut-1	Dowling-Degos disease
180601	Glyceraldehyde-3-phosphate dehydrogenase 3	gpd-3	Alzheimer's disease brain glioma diabetic retinopathy epilepsy lymphangioleiomyomatosis middle cerebral artery infarction obesity oral squamous cell carcinoma rheumatic heart disease
180583	ATP-dependent 6-phosphofructokinase 1	pfk-1.1	disease of metabolism glycogen storage disease VII glycogen storage disease
180533	Beta-hexosaminidase A	hex-1	Sandhoff disease Tay-Sachs disease lysosomal storage disease spinal muscular atrophy
180404	Putative UDP-glucuronosyltransferase ugt-46;glucuronosyltransferase	ugt-46
180302	Polypeptide N-acetylgalactosaminyltransferase 4;polypeptide N-acetylgalactosaminyltransferase	gly-4	congenital disorder of glycosylation type II
180290	Nucleoside hydrolase	Y43F8C.13
180244	Queuine tRNA-ribosyltransferase accessory subunit 2	tgt-2
180119	glycogenin glucosyltransferase	gyg-2	glycogen storage disease XV glycogen storage disease
179990	EGF domain-specific O-linked N-acetylglucosamine transferase;Heparan N-sulfatase	H12D21.10	Adams-Oliver syndrome
179890	N-acetylglucosaminyldiphosphodolichol N-acetylglucosaminyltransferase	algn-13	developmental and epileptic encephalopathy 36

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