GlyCosmos Portal

Danio rerio (zebrafish)

Summary

Taxonomy ID: 7955
PubChem Taxonomy: 7955

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

Displaying entries **676 - 700** of **748** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
553772	SREBF pathway regulator in golgi 1	spring1
337596	Rh family B glycoprotein	rhbg
414848	RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	rfng
100007702	R-spondin 3	rspo3
436625	R-spondin 1	rspo1
503760	POC1 centriolar protein homolog B (Chlamydomonas), like	poc1bl
402892	ORAI calcium release-activated calcium modulator 1b	orai1b
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
436629	NUS1 dehydrodolichyl diphosphate synthase subunit	nus1
282673	NPC intracellular cholesterol transporter 2, tandem duplicate 1	npc2.1
791161	NALCN channel auxiliary factor 2	nalf2
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
793524	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2a	ndst2a	autism spectrum disorder azoospermia intellectual disability
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
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
493602	N-acylsphingosine amidohydrolase 2	asah2
553365	N-acetylglucosamine-1-phosphate transferase subunits alpha and beta	gnptab	mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucolipidosis
393141	MYC proto-oncogene, bHLH transcription factor b	mycb
30686	MYC proto-oncogene, bHLH transcription factor a	myca
445176	MFSD2 lysolipid transporter A, lysophospholipid b	mfsd2ab
492810	MFSD2 lysolipid transporter A, lysophospholipid a	mfsd2aa
493633	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	mfng
100149102	LysM, putative peptidoglycan-binding, domain containing 4	lysmd4

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