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 ▼
407861	STT3A, subunit of the oligosaccharyltransferase complex (catalytic)	stt3a	congenital disorder of glycosylation Iw
394898	ALG11, alpha-1,2-mannosyltransferase	alg11	congenital disorder of glycosylation Ip
100497477	ALG9, alpha-1,2-mannosyltransferase	alg9	congenital disorder of glycosylation Il congenital disorder of glycosylation type I
594994	ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase	alg1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
100487779	dolichyl-phosphate (UDP-N-acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P transferase)	dpagt1	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
595052	ALG2, alpha-1,3/1,6-mannosyltransferase	alg2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
548388	ALG8, alpha-1,3-glucosyltransferase	alg8	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease
548874	ALG12, alpha-1,6-mannosyltransferase	alg12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
548940	mannose-P-dolichol utilization defect 1	mpdu1	congenital disorder of glycosylation If
496884	dolichyl-phosphate mannosyltransferase polypeptide 1, catalytic subunit	dpm1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
100127746	ALG3, alpha-1,3- mannosyltransferase	alg3	congenital disorder of glycosylation Id congenital disorder of glycosylation
496948	ALG6, alpha-1,3-glucosyltransferase	alg6	congenital disorder of glycosylation Ic congenital disorder of glycosylation type I
100485011	polypeptide N-acetylgalactosaminyltransferase 12	galnt12	colorectal cancer
100492586	heparan sulfate-glucosamine 3-sulfotransferase 2	hs3st2	colon cancer lung cancer lung non-small cell carcinoma pancreatic cancer
395003	diacylglycerol O-acyltransferase 2	dgat2	chronic kidney disease metabolic dysfunction-associated steatotic liver disease premature menopause steatotic liver disease
100038221	glucosaminyl (N-acetyl) transferase 2 (I blood group), gene 2	gcnt2.2	cataract 13 with adult i phenotype cataract
447974	fucosyltransferase 4	fut4	candidiasis
100495376	fucosyltransferase 6	fut6	candidiasis
548391	fucosyltransferase 9 (alpha (1,3) fucosyltransferase)	fut9	candidiasis
407879	protein phosphatase 1, catalytic subunit, gamma isozyme	ppp1cc	cancer congestive heart failure type 2 diabetes mellitus
100038162	triosephosphate isomerase 1	tpi1	cancer carbohydrate metabolic disorder neurodegenerative disease ocular hypertension triosephosphate isomerase deficiency
100488616	collagen beta(1-O)galactosyltransferase 1	colgalt1	brain small vessel disease 3
550067	citrate synthase	cs	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
100158586	transmembrane and tetratricopeptide repeat containing 4	tmtc4	autosomal recessive nonsyndromic deafness
402789	ST3 beta-galactoside alpha-2,3-sialyltransferase 3	st3gal3	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15 retinitis pigmentosa 33 retinitis pigmentosa

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