GlyCosmos Portal

Xenopus laevis (African clawed frog)

Summary

Taxonomy ID: 8355
PubChem Taxonomy: 8355

Genes (478) Glycans (43) Glycoproteins (658) Lectins (20)

Displaying entries **51 - 75** of **478** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
399170	AKT serine/threonine kinase 1 S homeolog	akt1.S	Cowden syndrome 6 Parkinson's disease Proteus syndrome bipolar disorder breast cancer chronic myeloid leukemia colon cancer colorectal cancer esophageal cancer esophagus squamous cell carcinoma idiopathic pulmonary fibrosis in situ carcinoma intermediate coronary syndrome invasive ductal carcinoma lung non-small cell carcinoma malignant astrocytoma myocardial infarction ovarian cancer pancreatic cancer pancreatic intraductal papillary-mucinous neoplasm prostate adenocarcinoma prostate cancer pulmonary tuberculosis renal cell carcinoma schizophrenia urinary bladder cancer vulva cancer
399204	UDP-glucose ceramide glucosyltransferase L homeolog	ugcg.L
399234	STT3A, subunit of the oligosaccharyltransferase complex (catalytic) L homeolog	stt3a.L	congenital disorder of glycosylation Iw
403360	dehydrogenase E1 and transketolase domain containing 1 L homeolog	dhtkd1.L	2-aminoadipic 2-oxoadipic aciduria Charcot-Marie-Tooth disease axonal type 2Q
414465	ST3 beta-galactoside alpha-2,3-sialyltransferase 2 gene 1 L homeolog	st3gal2.L
414536	heparan sulfate 2-O-sulfotransferase 1 S homeolog	hs2st1.S
414540	beta-1,4-galactosyltransferase 3 S homeolog	b4galt3.S
414570	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) L homeolog	pomgnt1.L	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2O congenital muscular dystrophy-dystroglycanopathy type A3 lissencephaly muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy retinitis pigmentosa
414590	mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase L homeolog	mgat2.L	congenital disorder of glycosylation type IIa
414623	fucosyltransferase 10 (alpha (1,3) fucosyltransferase) L homeolog	fut10.L
414647	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2 L homeolog	b3gnt2.L
414689	dolichyl-phosphate mannosyltransferase polypeptide 1, catalytic subunit L homeolog	dpm1.L	congenital disorder of glycosylation Ie
431849	ALG8, alpha-1,3-glucosyltransferase S homeolog	alg8.S	congenital disorder of glycosylation Ih polycystic liver disease
431874	beta-1,3-N-acetylgalactosaminyltransferase 2 L homeolog	b3galnt2.L	congenital muscular dystrophy-dystroglycanopathy type A11
431894	polypeptide N-acetylgalactosaminyltransferase 7 L homeolog	galnt7.L
431912	glycogen synthase 2 L homeolog	gys2.L
431927	ALG13, UDP-N-acetylglucosaminyltransferase subunit-like L homeolog	alg13l.L
432047	ALG10, alpha-1,2-glucosyltransferase S homeolog	alg10.S
432105	polypeptide N-acetylgalactosaminyltransferase 4 L homeolog	galnt4.L
432136	enolase superfamily member 1 S homeolog	enosf1.S
432177	glucosaminyl (N-acetyl) transferase 2 (I blood group), gene 2 S homeolog	gcnt2.2.S	cataract 13 with adult i phenotype cataract
432275	glucosaminyl (N-acetyl) transferase 2 (I blood group), gene 2 L homeolog	gcnt2.2.L	cataract 13 with adult i phenotype cataract
443852	protein phosphatase 1, catalytic subunit, beta isozyme L homeolog	ppp1cb.L	Noonan syndrome-like disorder with loose anagen hair 2
443855	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1 S homeolog	ndst1.S	autosomal recessive intellectual developmental disorder 46
443870	alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase A L homeolog	mgat4a.L	pancreatic cancer

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