GlyCosmos Portal

Danio rerio (zebrafish)

Summary

Taxonomy ID: 7955
PubChem Taxonomy: 7955

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

Displaying entries **201 - 225** of **358** in total

« First

‹ Prev

…

5

6

7

8

9

10

11

12

13

…

Next ›

Last »
Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
567859	collagen beta(1-O)galactosyltransferase 1b	colgalt1b	brain small vessel disease 3
568500	polypeptide N-acetylgalactosaminyltransferase 8a, tandem duplicate 2	galnt8a.2
568547	polypeptide N-acetylgalactosaminyltransferase 8a, tandem duplicate 1	galnt8a.1
568645	probable polypeptide N-acetylgalactosaminyltransferase 8	LOC568645
568868	interleukin 1 receptor accessory protein-like 1a	il1rapl1a	intellectual disability non-syndromic X-linked intellectual disability 21
568888	fucosyltransferase 11 (alpha (1,3) fucosyltransferase)	fut11	stomach cancer
568915	polypeptide N-acetylgalactosaminyltransferase like 6	galntl6
569036	YdjC chitooligosaccharide deacetylase homolog	ydjc
569353	heparan sulfate 6-O-sulfotransferase 3b	hs6st3b
569494	ALG12 alpha-1,6-mannosyltransferase	alg12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
569769	protein-O-mannosyltransferase 1	pomt1	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2K cardiomyopathy cleft lip congenital muscular dystrophy-dystroglycanopathy type A1 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy muscular dystrophy
570248	UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 2	galnt2	congenital disorder of glycosylation type II
570459	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1b	ndst1b	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
570828	beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase b	mgat3b
570913	UDP glucuronosyltransferase 5 family, polypeptide G1	ugt5g1
571003	UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 1b	b3galt1b
571246	heparan sulfate (glucosamine) 3-O-sulfotransferase 2	hs3st2	colon cancer lung cancer lung non-small cell carcinoma pancreatic cancer
571426	fukutin related protein	fkrp	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2I congenital muscular dystrophy-dystroglycanopathy type A5 dilated cardiomyopathy limb-girdle muscular dystrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy
571876	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)	pomgnt1	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2O congenital muscular dystrophy-dystroglycanopathy type A3 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy retinitis pigmentosa
572324	UDP-Gal:betaGal beta 1,3-galactosyltransferase polypeptide 6	b3galt6	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome spondyloepimetaphyseal dysplasia with joint laxity type 1
619261	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like 1	b3gntl1
641479	UDP glucuronosyltransferase 5 family, polypeptide A1	ugt5a1
641488	UDP glucuronosyltransferase 1 family, polypeptide A1	ugt1a1
641495	protein O-glucosyltransferase 1	poglut1	Dowling-Degos disease autosomal recessive limb-girdle muscular dystrophy type 2Z autosomal recessive limb-girdle muscular dystrophy
652952	O-linked N-acetylglucosamine (GlcNAc) transferase, tandem duplicate 2	ogt.2	aortic valve stenosis non-syndromic X-linked intellectual disability 106

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements