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 **76 - 100** of **320** in total

« First

‹ Prev

1

2

3

4

5

6

7

8

…

Next ›

Last »
Gene ID	Gene Name	Gene Symbol	Disease Ontology ▼
407846	ST6 beta-galactosamide alpha-2,6-sialyltranferase 2	st6gal2	autosomal recessive cutis laxa type IID developmental and epileptic encephalopathy 93
100158632	phosphatidylinositol glycan anchor biosynthesis class A	piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
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
448393	exostosin glycosyltransferase 1	ext1	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
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
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
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
100491268	ST6 beta-galactosamide alpha-2,6-sialyltranferase 1	st6gal1	alcohol use disorder high grade glioma
100170600	beta-1,4-glucuronyltransferase 1	b4gat1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A13 muscular dystrophy-dystroglycanopathy type B1
100145540	ribitol xylosyltransferase 1	rxylt1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A10
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
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
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
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
448225	C1GALT1 specific chaperone 1	c1galt1c1	Tn polyagglutination syndrome hemolytic-uremic syndrome
780006	beta 3-glucosyltransferase	b3glct	Peters plus syndrome
100496603	heparan sulfate 6-O-sulfotransferase 2	hs6st2	Paganini-Miozzo syndrome
496958	protein phosphatase 1, catalytic subunit, beta isozyme	ppp1cb	Noonan syndrome-like disorder with loose anagen hair 2 cancer
100124954	phosphoribosyl transferase domain containing 1	prtfdc1	Lesch-Nyhan syndrome
594895	beta-1,3-glucuronyltransferase 3	b3gat3	Larsen-like syndrome B3GAT3 type
100490155	glycogen synthase 1	gys1	Lafora disease cardiovascular system disease

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements