GlyCosmos Portal

Danio rerio (zebrafish)

Summary

Taxonomy ID: 7955
PubChem Taxonomy: 7955

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

Displaying entries **101 - 125** of **358** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
414848	RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	rfng
393985	queuine tRNA-ribosyltransferase 1	qtrt1
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
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
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
503760	POC1 centriolar protein homolog B (Chlamydomonas), like	poc1bl
556077	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	plod3	hepatocellular carcinoma hypothyroidism
100148642	phosphatidylinositol glycan anchor biosynthesis, class V	pigv	hyperphosphatasia with impaired intellectual development syndrome 1
393361	phosphatidylinositol glycan anchor biosynthesis, class M	pigm
393448	phosphatidylinositol glycan anchor biosynthesis, class B	pigb	developmental and epileptic encephalopathy 80 sleeping sickness
791759	phosphatidylinositol glycan anchor biosynthesis, class A	piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
777617	protein-glucosylgalactosylhydroxylysine glucosidase	pgghg
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
652952	O-linked N-acetylglucosamine (GlcNAc) transferase, tandem duplicate 2	ogt.2	aortic valve stenosis non-syndromic X-linked intellectual disability 106
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
100317129	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	ndst3	autism spectrum disorder azoospermia intellectual disability
798226	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2b	ndst2b	autism spectrum disorder azoospermia intellectual disability

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