GlyCosmos Portal

Xenopus tropicalis (tropical clawed frog)

Summary

Taxonomy ID: 8364
PubChem Taxonomy: 8364

Genes (320) Glycans (10) Glycoproteins (267) Lectins (10) Pathways (145)

Displaying entries **26 - 50** of **320** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
780006	beta 3-glucosyltransferase	b3glct	Peters plus syndrome
448225	C1GALT1 specific chaperone 1	c1galt1c1	Tn polyagglutination syndrome hemolytic-uremic syndrome
100145309	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
448433	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
100490100	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
100158594	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
100145540	ribitol xylosyltransferase 1	rxylt1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A10
100170600	beta-1,4-glucuronyltransferase 1	b4gat1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A13 muscular dystrophy-dystroglycanopathy type B1
100491268	ST6 beta-galactosamide alpha-2,6-sialyltranferase 1	st6gal1	alcohol use disorder high grade glioma
448158	protein phosphatase 1 regulatory subunit 3C gene 2	ppp1r3c.2	alcohol use disorder
548704	protein phosphatase 1 regulatory subunit 3B	ppp1r3b	alcohol use disorder
553157	O-linked N-acetylglucosamine (GlcNAc) transferase	ogt	aortic valve stenosis congestive heart failure diabetes mellitus non-syndromic X-linked intellectual disability 106 type 2 diabetes mellitus
100145653	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	ndst3	autism spectrum disorder azoospermia intellectual disability
100217321	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	ndst2	autism spectrum disorder azoospermia intellectual disability
100380006	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 4	ndst4	autism spectrum disorder azoospermia intellectual disability
448393	exostosin glycosyltransferase 1	ext1	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
100487794	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1	c1galt1	autoimmune disease of blood
100496837	provisional ortholog of core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1	XB5871033	autoimmune disease of blood
100158632	phosphatidylinositol glycan anchor biosynthesis class A	piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
407846	ST6 beta-galactosamide alpha-2,6-sialyltranferase 2	st6gal2	autosomal recessive cutis laxa type IID developmental and epileptic encephalopathy 93
402789	ST3 beta-galactoside alpha-2,3-sialyltransferase 3	st3gal3	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15 retinitis pigmentosa 33 retinitis pigmentosa
100158586	transmembrane and tetratricopeptide repeat containing 4	tmtc4	autosomal recessive nonsyndromic deafness
550067	citrate synthase	cs	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
100488616	collagen beta(1-O)galactosyltransferase 1	colgalt1	brain small vessel disease 3
100038162	triosephosphate isomerase 1	tpi1	cancer carbohydrate metabolic disorder neurodegenerative disease ocular hypertension triosephosphate isomerase deficiency

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