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 **126 - 150** of **320** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
100127708	glucoside xylosyltransferase 1	gxylt1
100127746	ALG3, alpha-1,3- mannosyltransferase	alg3	congenital disorder of glycosylation Id congenital disorder of glycosylation
100135191	UDP glucuronosyltransferase 1 family, polypeptide A6	ugt1a6	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome bilirubin metabolic disorder breast cancer cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer type 1 diabetes mellitus type 2 diabetes mellitus
100144948	enolase 4	eno4
100144979	xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7	b4galt7	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
100145063	idnK, gluconokinase homolog (E. coli)	idnk
100145173	galactose-3-O-sulfotransferase 4, gene 6	gal3st4.6
100145200	solute carrier family 23 (ascorbic acid transporter), member 2	slc23a2
100145208	beta-1,4-N-acetyl-galactosaminyl transferase 1	b4galnt1	hereditary spastic paraplegia 26
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
100145490	xylosyltransferase I	xylt1	Desbuquois dysplasia kidney disease pseudoxanthoma elasticum type 1 diabetes mellitus
100145518	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1, gene 1	b4galt1.1	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease
100145540	ribitol xylosyltransferase 1	rxylt1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A10
100145551	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	mgat5	proteinuria
100145562	heparan sulfate 2-O-sulfotransferase 1	hs2st1
100145573	transmembrane and tetratricopeptide repeat containing 3	tmtc3	epilepsy lissencephaly 8
100145594	alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase D	mgat4d
100145625	ALG13 UDP-N-acetylglucosaminyltransferase subunit	alg13
100145653	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	ndst3	autism spectrum disorder azoospermia intellectual disability
100145701	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3, gene 2	b3gnt3.2
100145711	hyaluronan synthase 2	has2	diabetes insipidus middle cerebral artery infarction pulmonary hypertension
100145746	hyaluronan synthase 1 like	has1l	pulmonary hypertension
100145769	phosphatidylinositol glycan anchor biosynthesis class B	pigb
100145790	heparan sulfate-glucosamine 3-sulfotransferase 5	hs3st5
100151709	exostosin glycosyltransferase 2	ext2	hereditary multiple exostoses

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