GlyCosmos Portal

Danio rerio (zebrafish)

Summary

Taxonomy ID: 7955
PubChem Taxonomy: 7955

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

Displaying entries **226 - 250** of **358** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
724006	alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	mgat5	proteinuria
101884072	mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase, isozyme B	mgat5b
447806	mannose-P-dolichol utilization defect 1a	mpdu1a	congenital disorder of glycosylation If
415220	mannose-P-dolichol utilization defect 1b	mpdu1b	congenital disorder of glycosylation If
393526	methylthioadenosine phosphorylase	mtap	biliary tract benign neoplasm common bile duct neoplasm diaphyseal medullary stenosis with malignant fibrous histiocytoma pancreatic cancer
100329944	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1a	ndst1a	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
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
793524	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2a	ndst2a	autism spectrum disorder azoospermia intellectual disability
798226	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2b	ndst2b	autism spectrum disorder azoospermia intellectual disability
100317129	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	ndst3	autism spectrum disorder azoospermia intellectual disability
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
652952	O-linked N-acetylglucosamine (GlcNAc) transferase, tandem duplicate 2	ogt.2	aortic valve stenosis non-syndromic X-linked intellectual disability 106
560788	poly (ADP-ribose) polymerase 1	parp1	Alzheimer's disease Huntington's disease Parkinson's disease arthritis asthma autoimmune disease bacterial meningitis borna disease congestive heart failure idiopathic pulmonary fibrosis kidney failure leiomyoma liver cirrhosis middle cerebral artery infarction nephritis perinatal necrotizing enterocolitis stomach cancer stomach carcinoma transient cerebral ischemia type 2 diabetes mellitus ureteral obstruction
777617	protein-glucosylgalactosylhydroxylysine glucosidase	pgghg
791759	phosphatidylinositol glycan anchor biosynthesis, class A	piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
393448	phosphatidylinositol glycan anchor biosynthesis, class B	pigb	developmental and epileptic encephalopathy 80 sleeping sickness
393361	phosphatidylinositol glycan anchor biosynthesis, class M	pigm
100148642	phosphatidylinositol glycan anchor biosynthesis, class V	pigv	hyperphosphatasia with impaired intellectual development syndrome 1
556077	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	plod3	hepatocellular carcinoma hypothyroidism
503760	POC1 centriolar protein homolog B (Chlamydomonas), like	poc1bl
403029	protein O-fucosyltransferase 1	pofut1	Dowling-Degos disease
777668	protein O-fucosyltransferase 2	pofut2	Down syndrome
641495	protein O-glucosyltransferase 1	poglut1	Dowling-Degos disease autosomal recessive limb-girdle muscular dystrophy type 2Z autosomal recessive limb-girdle muscular dystrophy
393905	protein O-glucosyltransferase 2	poglut2
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

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