GlyCosmos Portal

Xenopus tropicalis (tropical clawed frog)

Summary

Taxonomy ID: 8364
PubChem Taxonomy: 8364

Genes (459) Glycans (10) Glycoproteins (269) Lectins (10) Pathways (156)

Displaying entries **376 - 400** of **459** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
496641	beta-1,3-N-acetylgalactosaminyltransferase 2	b3galnt2	congenital muscular dystrophy-dystroglycanopathy type A11
100216215	aspartate beta-hydroxylase domain containing 2	asphd2
613084	apelin receptor	aplnr
448576	adenomatosis polyposis coli down-regulated 1	apcdd1
100497477	ALG9, alpha-1,2-mannosyltransferase	alg9	congenital disorder of glycosylation Il congenital disorder of glycosylation type I
548388	ALG8, alpha-1,3-glucosyltransferase	alg8	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease
496948	ALG6, alpha-1,3-glucosyltransferase	alg6	congenital disorder of glycosylation Ic congenital disorder of glycosylation type I
448472	ALG5, dolichyl-phosphate beta-glucosyltransferase	alg5	congenital disorder of glycosylation type I polycystic kidney disease
100127746	ALG3, alpha-1,3- mannosyltransferase	alg3	congenital disorder of glycosylation Id congenital disorder of glycosylation
595052	ALG2, alpha-1,3/1,6-mannosyltransferase	alg2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
100379745	ALG14, UDP-N-acetylglucosaminyltransferase subunit	alg14	congenital myasthenic syndrome 15
549862	ALG13, UDP-N-acetylglucosaminyltransferase subunit-like	alg13l	developmental and epileptic encephalopathy 36
100145625	ALG13 UDP-N-acetylglucosaminyltransferase subunit	alg13
548874	ALG12, alpha-1,6-mannosyltransferase	alg12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
394898	ALG11, alpha-1,2-mannosyltransferase	alg11	congenital disorder of glycosylation Ip
548946	ALG10, alpha-1,2-glucosyltransferase	alg10	long QT syndrome 2 nonsyndromic deafness
594994	ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase	alg1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
548938	ADP-ribosylserine hydrolase	adprs	stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
100488158	ADAM metallopeptidase with thrombospondin type 1 motif 5	adamts5
100151734	ADAM metallopeptidase with thrombospondin type 1 motif 1	adamts1
493572	acid phosphatase 5, tartrate resistant	acp5
100144634	angiotensin I converting enzyme	ace
100489217	alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2-like	abo2
100497509	ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase) gene 4	abo.4	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome
549437	ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase) gene 3	abo.3	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome

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