GlyCosmos Portal

Danio rerio (zebrafish)

Summary

Taxonomy ID: 7955
PubChem Taxonomy: 7955

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

Displaying entries **51 - 75** of **748** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
100317129	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	ndst3	autism spectrum disorder azoospermia intellectual disability
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
497279	exostosin glycosyltransferase 1a	ext1a	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
497280	exostosin glycosyltransferase 1b	ext1b	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
555344	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1a	c1galt1a	autoimmune disease of blood
337131	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1, like b	c1galt1lb	autoimmune disease of blood
557675	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1, like a	c1galt1la	autoimmune disease of blood
792692	aldolase C, fructose-bisphosphate, a	aldoca	autoimmune disease of the nervous system borna disease hepatocellular carcinoma
369193	aldolase C, fructose-bisphosphate, b	aldocb	autoimmune disease of the nervous system borna disease hepatocellular carcinoma
791759	phosphatidylinositol glycan anchor biosynthesis, class A	piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
393326	ST3 beta-galactoside alpha-2,3-sialyltransferase 3a	st3gal3a	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
407659	ST3 beta-galactoside alpha-2,3-sialyltransferase 3b	st3gal3b	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
560605	transmembrane O-mannosyltransferase targeting cadherins 4	tmtc4	autosomal recessive nonsyndromic deafness
393526	methylthioadenosine phosphorylase	mtap	biliary tract benign neoplasm common bile duct neoplasm diaphyseal medullary stenosis with malignant fibrous histiocytoma pancreatic cancer
322339	citrate synthase	cs	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
565862	collagen beta(1-O)galactosyltransferase 1a	colgalt1a	brain small vessel disease 3
567859	collagen beta(1-O)galactosyltransferase 1b	colgalt1b	brain small vessel disease 3
560753	triosephosphate isomerase 1b	tpi1b	cancer carbohydrate metabolic disorder neurodegenerative disease ocular hypertension triosephosphate isomerase deficiency
192309	triosephosphate isomerase 1a	tpi1a	cancer carbohydrate metabolic disorder neurodegenerative disease ocular hypertension triosephosphate isomerase deficiency
562250	fucosyltransferase 7 (alpha (1,3) fucosyltransferase)	fut7	candidiasis
503885	fucosyltransferase 9d	fut9d	candidiasis
796410	fucosyltransferase 9a	fut9a	candidiasis
100124609	zgc:165582	zgc:165582	candidiasis
792063	alpha(1,3)fucosyltransferase gene 2	ft2	candidiasis

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