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 **151 - 175** of **320** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
100380178	Beta-1,3-galactosyltransferase 2 like	b3galt2l
100380167	heparan sulfate-glucosamine 3-sulfotransferase 3A1	hs3st3a1
100380117	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3, gene 1	b3gnt3.1
100380058	UDP-glucose glycoprotein glucosyltransferase 1	uggt1
100380028	phosphatidylinositol glycan anchor biosynthesis class V	pigv	hyperphosphatasia with impaired intellectual development syndrome 1
100380006	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 4	ndst4	autism spectrum disorder azoospermia intellectual disability
100379780	chondroitin polymerizing factor	chpf
100379745	ALG14, UDP-N-acetylglucosaminyltransferase subunit	alg14	congenital myasthenic syndrome 15
100379720	carbohydrate (N-acetylglucosamine 6-O) sulfotransferase 7	chst7
100335040	fucosyltransferase 7 (alpha (1,3) fucosyltransferase)	fut7
100329192	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6	st6galnac6
100329191	ST3 beta-galactoside alpha-2,3-sialyltransferase 5	st3gal5	salt and pepper syndrome
100329190	ST3 beta-galactoside alpha-2,3-sialyltransferase 1	st3gal1
100217321	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	ndst2	autism spectrum disorder azoospermia intellectual disability
100216189	chondroitin polymerizing factor 2	chpf2
100170600	beta-1,4-glucuronyltransferase 1	b4gat1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A13 muscular dystrophy-dystroglycanopathy type B1
100170561	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2	b3gnt2
100158632	phosphatidylinositol glycan anchor biosynthesis class A	piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
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
100158586	transmembrane and tetratricopeptide repeat containing 4	tmtc4	autosomal recessive nonsyndromic deafness
100151709	exostosin glycosyltransferase 2	ext2	hereditary multiple exostoses
100145790	heparan sulfate-glucosamine 3-sulfotransferase 5	hs3st5
100145769	phosphatidylinositol glycan anchor biosynthesis class B	pigb
100145746	hyaluronan synthase 1 like	has1l	pulmonary hypertension
100145711	hyaluronan synthase 2	has2	diabetes insipidus middle cerebral artery infarction pulmonary hypertension

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