GlyCosmos Portal

Xenopus laevis (African clawed frog)

Summary

Taxonomy ID: 8355
PubChem Taxonomy: 8355

Genes (478) Glycans (43) Glycoproteins (658) Lectins (20)

Displaying entries **26 - 50** of **478** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
100127336	beta 3-glucosyltransferase L homeolog	b3glct.L	Peters plus syndrome
495031	C1GALT1 specific chaperone 1 L homeolog	c1galt1c1.L	Tn polyagglutination syndrome hemolytic-uremic syndrome
108700090	C1GALT1 specific chaperone 1 S homeolog	c1galt1c1.S	Tn polyagglutination syndrome hemolytic-uremic syndrome
108698503	fukutin related protein L homeolog	fkrp.L	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 B5 muscular dystrophy
108699937	protein-O-mannosyltransferase 1 S homeolog	pomt1.S	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
108698684	protein-O-mannosyltransferase 2 L homeolog	pomt2.L	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
495292	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) S homeolog	pomgnt1.S	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2O congenital muscular dystrophy-dystroglycanopathy type A3 lissencephaly muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy retinitis pigmentosa
414570	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) L homeolog	pomgnt1.L	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2O congenital muscular dystrophy-dystroglycanopathy type A3 lissencephaly muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy retinitis pigmentosa
447370	oxoglutarate dehydrogenase like L homeolog	ogdhl.L	Yoon-Bellen neurodevelopmental syndrome
108718183	ST6 beta-galactosamide alpha-2,6-sialyltranferase 1 S homeolog	st6gal1.S	alcohol use disorder
108717116	ST6 beta-galactosamide alpha-2,6-sialyltranferase 1 L homeolog	st6gal1.L	alcohol use disorder
446517	mannosidase, endo-alpha L homeolog	manea.L	anxiety disorder cocaine dependence panic disorder
447694	O-linked N-acetylglucosamine (GlcNAc) transferase L homeolog	ogt.L	aortic valve stenosis non-syndromic X-linked intellectual disability 106
108717884	uronyl-2-sulfotransferase S homeolog	ust.S	attention deficit hyperactivity disorder
108715547	CMP-N-acetylneuraminate-beta-1,4-galactoside alpha-2,3-sialyltransferase	LOC108715547	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
443855	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 S homeolog	ndst1.S	autosomal recessive intellectual developmental disorder 46
108710821	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 L homeolog	ndst1.L	autosomal recessive intellectual developmental disorder 46
108708472	transmembrane and tetratricopeptide repeat containing 4 L homeolog	tmtc4.L	autosomal recessive nonsyndromic deafness
495521	collagen beta(1-O)galactosyltransferase 1 S homeolog	colgalt1.S	brain small vessel disease 3
100125229	collagen beta(1-O)galactosyltransferase 1 L homeolog	colgalt1.L	brain small vessel disease 3
380168	triosephosphate isomerase 1 S homeolog	tpi1.S	carbohydrate metabolic disorder triosephosphate isomerase deficiency
108697802	glycogen synthase 1 S homeolog	gys1.S	cardiovascular system disease
108696758	glycogen synthase 1 L homeolog	gys1.L	cardiovascular system disease
432177	glucosaminyl (N-acetyl) transferase 2 (I blood group), gene 2 S homeolog	gcnt2.2.S	cataract 13 with adult i phenotype cataract
432275	glucosaminyl (N-acetyl) transferase 2 (I blood group), gene 2 L homeolog	gcnt2.2.L	cataract 13 with adult i phenotype cataract

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