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 **51 - 75** of **320** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
496958	protein phosphatase 1, catalytic subunit, beta isozyme	ppp1cb	Noonan syndrome-like disorder with loose anagen hair 2 cancer
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
496628	protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)	pomgnt2	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
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
493476	protein O-glucosyltransferase 1	poglut1
779585	protein O-fucosyltransferase 2	pofut2	Down syndrome
496411	protein O-fucosyltransferase 1	pofut1	Dowling-Degos disease
734090	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	plod3	hepatocellular carcinoma hypothyroidism
100497115	phosphatidylinositol glycan anchor biosynthesis class Z	pigz
100380028	phosphatidylinositol glycan anchor biosynthesis class V	pigv	hyperphosphatasia with impaired intellectual development syndrome 1
493482	phosphatidylinositol glycan anchor biosynthesis class M	pigm
100145769	phosphatidylinositol glycan anchor biosynthesis class B	pigb
100158632	phosphatidylinositol glycan anchor biosynthesis class A	piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
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
100380006	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 4	ndst4	autism spectrum disorder azoospermia intellectual disability
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
496577	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1	ndst1	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
548940	mannose-P-dolichol utilization defect 1	mpdu1	congenital disorder of glycosylation If
496754	monoacylglycerol O-acyltransferase 2, gene 1	mogat2
734060	monoacylglycerol O-acyltransferase 1	mogat1
100487001	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B	mgat5b
100145551	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	mgat5	proteinuria
100489718	MGAT4 family member G	mgat4g

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