GlyCosmos Portal

Danio rerio (zebrafish)

Summary

Taxonomy ID: 7955
PubChem Taxonomy: 7955

Genes (748) Glycans (175) Glycoproteins (596) Lectins (18) Pathways (261)

Displaying entries **101 - 125** of **748** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▼
798226	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2b	ndst2b	autism spectrum disorder azoospermia intellectual disability
557218	uronyl 2-sulfotransferase a	usta	attention deficit hyperactivity disorder
652952	O-linked N-acetylglucosamine (GlcNAc) transferase, tandem duplicate 2	ogt.2	aortic valve stenosis non-syndromic X-linked intellectual disability 106
337685	O-linked N-acetylglucosamine (GlcNAc) transferase, tandem duplicate 1	ogt.1	aortic valve stenosis congestive heart failure diabetes mellitus non-syndromic X-linked intellectual disability 106 type 2 diabetes mellitus
403143	sterile alpha and TIR motif containing 1	sarm1	amyotrophic lateral sclerosis neurodegenerative disease
327285	protein phosphatase 1, regulatory subunit 3B	ppp1r3b	alcohol use disorder
393807	protein phosphatase 1, regulatory subunit 3Cb	ppp1r3cb	alcohol use disorder type 2 diabetes mellitus
445376	ST6 beta-galactosamide alpha-2,6-sialyltranferase 1	st6gal1	alcohol use disorder high grade glioma
101669768	beta-1,4-glucuronyltransferase 1	b4gat1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A13 muscular dystrophy-dystroglycanopathy type B1
557187	ribitol xylosyltransferase 1	rxylt1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A10
571876	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)	pomgnt1	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2O congenital muscular dystrophy-dystroglycanopathy type A3 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy retinitis pigmentosa
563878	protein-O-mannosyltransferase 2	pomt2	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy congenital muscular dystrophy-dystroglycanopathy type A2 lissencephaly muscular dystrophy-dystroglycanopathy type B2 muscular dystrophy-dystroglycanopathy muscular dystrophy
569769	protein-O-mannosyltransferase 1	pomt1	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2K cardiomyopathy cleft lip congenital muscular dystrophy-dystroglycanopathy type A1 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy muscular dystrophy
571426	fukutin related protein	fkrp	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2I congenital muscular dystrophy-dystroglycanopathy type A5 dilated cardiomyopathy limb-girdle muscular dystrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy
324052	C1GALT1-specific chaperone 1	c1galt1c1	Tn polyagglutination syndrome hemolytic-uremic syndrome
799443	beta 3-glucosyltransferase a	b3glcta	Peters plus syndrome
564156	beta 3-glucosyltransferase b	b3glctb	Peters plus syndrome
768121	forkhead box O1 a	foxo1a	Parkinson's disease alveolar rhabdomyosarcoma congestive heart failure hepatocellular carcinoma metabolic dysfunction-associated steatotic liver disease prostate cancer
378450	heparan sulfate 6-O-sulfotransferase 2	hs6st2	Paganini-Miozzo syndrome
192334	beta-1,3-glucuronyltransferase 3 (glucuronosyltransferase I)	b3gat3	Larsen-like syndrome B3GAT3 type
373082	glycogen synthase 2	gys2	Lafora disease glycogen storage disease
394155	glycogen synthase 1 (muscle)	gys1	Lafora disease cardiovascular system disease
768123	DP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1, like	b4galt1l	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease
550425	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	b4galt1	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease
100006345	fukutin	fktn	Fukuyama congenital muscular dystrophy Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M dilated cardiomyopathy 1B dilated cardiomyopathy 1X muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B4 muscular dystrophy

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