GlyCosmos Portal

Danio rerio (zebrafish)

Summary

Taxonomy ID: 7955
PubChem Taxonomy: 7955

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

Displaying entries **26 - 50** of **358** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
100002270	si:ch73-62b13.1	si:ch73-62b13.1
795008	si:ch211-269c21.2	si:ch211-269c21.2
563347	si:ch211-264e16.2	si:ch211-264e16.2
101886093	si:ch211-264e16.1	si:ch211-264e16.1
565671	si:ch211-236h17.3	si:ch211-236h17.3
563138	si:ch211-219a15.4	si:ch211-219a15.4
100329339	si:ch211-216b21.2	si:ch211-216b21.2
557187	ribitol xylosyltransferase 1	rxylt1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A10
403070	regucalcin	rgn	familial hyperlipidemia hepatocellular carcinoma stomach cancer
393985	queuine tRNA-ribosyltransferase 1	qtrt1
777617	protein-glucosylgalactosylhydroxylysine glucosidase	pgghg
563878	protein-O-mannosyltransferase 2	pomt2	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy congenital muscular dystrophy-dystroglycanopathy type A2 lissencephaly muscular dystrophy-dystroglycanopathy type B2 muscular dystrophy-dystroglycanopathy muscular dystrophy
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
393807	protein phosphatase 1, regulatory subunit 3Cb	ppp1r3cb	alcohol use disorder type 2 diabetes mellitus
327285	protein phosphatase 1, regulatory subunit 3B	ppp1r3b	alcohol use disorder
492773	protein O-mannose kinase	pomk	congenital muscular dystrophy-dystroglycanopathy type A12 hydrocephalus muscular dystrophy-dystroglycanopathy type C12
497644	protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)	pomgnt2	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
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
393905	protein O-glucosyltransferase 2	poglut2
641495	protein O-glucosyltransferase 1	poglut1	Dowling-Degos disease autosomal recessive limb-girdle muscular dystrophy type 2Z autosomal recessive limb-girdle muscular dystrophy
777668	protein O-fucosyltransferase 2	pofut2	Down syndrome
403029	protein O-fucosyltransferase 1	pofut1	Dowling-Degos disease
556077	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	plod3	hepatocellular carcinoma hypothyroidism
568645	probable polypeptide N-acetylgalactosaminyltransferase 8	LOC568645
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

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