GlyCosmos Portal

Displaying entries **26 - 50** of **186** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
190668	Beta-1,4-N-acetylgalactosaminyltransferase bre-4	bre-4	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease multiple sclerosis
187430	Beta-1,4-galactosyltransferase galt-1	galt-1
176332	Beta-1,4-mannosyltransferase bre-3	bre-3
180533	Beta-hexosaminidase A	hex-1	Sandhoff disease Tay-Sachs disease lysosomal storage disease spinal muscular atrophy
191628	C-mannosyltransferase dpy-19	dpy-19	spermatogenic failure 9
188169	Ceramide glucosyltransferase 1	cgt-1	hypertension
181790	Ceramide glucosyltransferase 2	cgt-2	hypertension
174001	Ceramide glucosyltransferase 3	cgt-3	hypertension
172508	Chitin synthase chs-1	chs-1
173405	Chitin synthase chs-2;chitin synthase	chs-2
177464	Chitinase-like protein C25A8.4	cht-3
175920	Chitobiosyldiphosphodolichol beta-mannosyltransferase	algn-1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
176231	Chondroitin sulfate synthase mig-22	mig-22
172851	Chondroitin sulfate synthase sqv-5;Hexosyltransferase	sqv-5	temtamy preaxial brachydactyly syndrome
172855	Dol-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-Dol alpha-1,2-glucosyltransferase	algn-10	long QT syndrome 2 nonsyndromic deafness
175065	Dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase	algn-3	congenital disorder of glycosylation Id congenital disorder of glycosylation
176874	Dolichol-phosphate mannosyltransferase subunit 1	dpm-1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
175886	Dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit stt-3	stt-3	congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix
178822	Dolichyl-phosphate beta-glucosyltransferase;dolichyl-phosphate beta-glucosyltransferase	algn-5	congenital disorder of glycosylation type I polycystic kidney disease
179990	EGF domain-specific O-linked N-acetylglucosamine transferase;Heparan N-sulfatase	H12D21.10	Adams-Oliver syndrome
187770	Endonuclease III homolog	nth-1	familial adenomatous polyposis 3
174423	Enolase	enol-1	Alzheimer's disease Parkinsonism aortic valve stenosis brain disease breast carcinoma hypertension migraine without aura neuroendocrine carcinoma prostate cancer toxic shock syndrome urinary bladder cancer visual epilepsy
178080	Exostosin-1 homolog	rib-1	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
176502	Exostosin-2 homolog	rib-2	hereditary multiple exostoses
177363	Fructose-2,6-bisphosphatase	pfkb-1.2	hyperinsulinism

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