GlyCosmos Portal

Danio rerio (zebrafish)

Summary

Taxonomy ID: 7955
PubChem Taxonomy: 7955

Genes (358) Glycans (175) Glycoproteins (592) Lectins (18) Pathways (252)

Displaying entries **1 - 25** of **358** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
30158	LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	lfng	spondylocostal dysostosis 3
30262	preproinsulin	ins	Alzheimer's disease cholangiocarcinoma diabetes mellitus diabetic retinopathy disease of metabolism gestational diabetes hyperinsulinism hypertension hyperuricemia insulinoma maturity-onset diabetes of the young type 10 maturity-onset diabetes of the young neonatal diabetes osteoarthritis pancreatic cancer pancreatic ductal carcinoma permanent neonatal diabetes mellitus prostate cancer sleep disorder steatotic liver disease type 1 diabetes mellitus 2 type 1 diabetes mellitus type 2 diabetes mellitus
192309	triosephosphate isomerase 1a	tpi1a	cancer carbohydrate metabolic disorder neurodegenerative disease ocular hypertension triosephosphate isomerase deficiency
192315	UDP-glucuronate decarboxylase 1	uxs1
192334	beta-1,3-glucuronyltransferase 3 (glucuronosyltransferase I)	b3gat3	Larsen-like syndrome B3GAT3 type
260350	hyaluronan synthase 2	has2	diabetes insipidus middle cerebral artery infarction pulmonary hypertension
266797	STT3 oligosaccharyltransferase complex catalytic subunit A	stt3a	congenital disorder of glycosylation Iw
282555	hyaluronan synthase 3	has3	pulmonary hypertension
286748	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7	b3gnt7
317743	glyceraldehyde-3-phosphate dehydrogenase	gapdh	Alzheimer's disease brain glioma diabetic retinopathy epilepsy lymphangioleiomyomatosis middle cerebral artery infarction obesity oral squamous cell carcinoma rheumatic heart disease
321664	aldolase b, fructose-bisphosphate	aldob	hereditary fructose intolerance syndrome liver benign neoplasm peritonitis type 2 diabetes mellitus
322339	citrate synthase	cs	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
322378	UDP glucuronosyltransferase 5 family, polypeptide A3	ugt5a3
322468	chitin synthase 1	chs1
322609	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3	st6galnac3
323918	STT3 oligosaccharyltransferase complex catalytic subunit B	stt3b	congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix
324052	C1GALT1-specific chaperone 1	c1galt1c1	Tn polyagglutination syndrome hemolytic-uremic syndrome
324407	chondroitin sulfate synthase 1	chsy1	temtamy preaxial brachydactyly syndrome
324510	glucosaminyl (N-acetyl) transferase 4a	gcnt4a
327285	protein phosphatase 1, regulatory subunit 3B	ppp1r3b	alcohol use disorder
327601	ALG8 alpha-1,3-glucosyltransferase	alg8	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease
334161	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	alg1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
336526	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5a	b3gnt5a
337131	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1, like b	c1galt1lb	autoimmune disease of blood
337225	chitinase domain containing 1	chid1

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