GlyCosmos Portal

Danio rerio (zebrafish)

Summary

Taxonomy ID: 7955
PubChem Taxonomy: 7955

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

Displaying entries **326 - 350** of **358** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
393326	ST3 beta-galactoside alpha-2,3-sialyltransferase 3a	st3gal3a	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
387303	globoside alpha-1,3-N-acetylgalactosaminyltransferase 1, like 4	gbgt1l4	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
378450	heparan sulfate 6-O-sulfotransferase 2	hs6st2	Paganini-Miozzo syndrome
373082	glycogen synthase 2	gys2	Lafora disease glycogen storage disease
369193	aldolase C, fructose-bisphosphate, b	aldocb	autoimmune disease of the nervous system borna disease hepatocellular carcinoma
368477	chondroitin sulfate synthase 3	chsy3
368327	dpy-19-like 1, like (H. sapiens)	dpy19l1l	spermatogenic failure 9
337685	O-linked N-acetylglucosamine (GlcNAc) transferase, tandem duplicate 1	ogt.1	aortic valve stenosis congestive heart failure diabetes mellitus non-syndromic X-linked intellectual disability 106 type 2 diabetes mellitus
337225	chitinase domain containing 1	chid1
337131	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1, like b	c1galt1lb	autoimmune disease of blood
336526	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 5a	b3gnt5a
334161	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	alg1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
327601	ALG8 alpha-1,3-glucosyltransferase	alg8	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease
327285	protein phosphatase 1, regulatory subunit 3B	ppp1r3b	alcohol use disorder
324510	glucosaminyl (N-acetyl) transferase 4a	gcnt4a
324407	chondroitin sulfate synthase 1	chsy1	temtamy preaxial brachydactyly syndrome
324052	C1GALT1-specific chaperone 1	c1galt1c1	Tn polyagglutination syndrome hemolytic-uremic syndrome
323918	STT3 oligosaccharyltransferase complex catalytic subunit B	stt3b	congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix
322609	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3	st6galnac3
322468	chitin synthase 1	chs1
322378	UDP glucuronosyltransferase 5 family, polypeptide A3	ugt5a3
322339	citrate synthase	cs	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
321664	aldolase b, fructose-bisphosphate	aldob	hereditary fructose intolerance syndrome liver benign neoplasm peritonitis type 2 diabetes mellitus
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
286748	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7	b3gnt7

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