GlyCosmos Portal

Danio rerio (zebrafish)

Summary

Taxonomy ID: 7955
PubChem Taxonomy: 7955

Genes (748) Glycans (175) Glycoproteins (596) Lectins (18) Pathways (261)

Displaying entries **226 - 250** of **748** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
30295	rhodopsin	rho
337596	Rh family B glycoprotein	rhbg
798402	rhomboid 5 homolog 1a (Drosophila)	rhbdf1a
403070	regucalcin	rgn	familial hyperlipidemia hepatocellular carcinoma stomach cancer
414848	RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	rfng
30512	ret proto-oncogene receptor tyrosine kinase	ret
100334698	reversion-inducing-cysteine-rich protein with kazal motifs	reck
393985	queuine tRNA-ribosyltransferase 1	qtrt1
436703	2-phosphoxylose phosphatase 1	pxylp1
799867	protein tyrosine phosphatase receptor type Fb	ptprfb
564097	patched domain containing 4	ptchd4
563834	protogenin homolog a (Gallus gallus)	prtga
322857	prominin 1a	prom1a
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
415107	popeye domain cAMP effector 1	popdc1
447803	paraoxonase 1	pon1
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

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