GlyCosmos Portal

Drosophila melanogaster (fruit fly)

Summary

Taxonomy ID: 7227
PubChem Taxonomy: 7227

Genes (311) Glycans (91) Glycoproteins (923) Lectins (38) Pathways (597)

Displaying entries **101 - 125** of **311** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
35307	UDP-glycosyltransferase family 37 member A1	Ugt37A1	hepatitis B
35486	super sex combs	sxc	aortic valve stenosis congestive heart failure diabetes mellitus non-syndromic X-linked intellectual disability 106 type 2 diabetes mellitus
35569	Heparan sulfate C5-epimerase	Hsepi	cerebrovascular disease hypertension
35570	Post-GPI attachment to proteins 3	PGAP3	hyperphosphatasia with impaired intellectual development syndrome 4
35627	Polypeptide N-Acetylgalactosaminyltransferase 3	Pgant3	hyperphosphatemic familial tumoral calcinosis
35728	Glyceraldehyde 3 phosphate dehydrogenase 1	Gapdh1	Alzheimer's disease brain glioma diabetic retinopathy epilepsy lymphangioleiomyomatosis middle cerebral artery infarction obesity oral squamous cell carcinoma rheumatic heart disease
35792	uncharacterized protein	CG8708
35824	Maltase A1	Mal-A1	cystinuria
35825	Maltase A2	Mal-A2	cystinuria
35826	Maltase A3	Mal-A3	cystinuria
35848	beta-1,3-Galactosyltransferase II	beta3GalTII	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome spondyloepimetaphyseal dysplasia with joint laxity type 1
35859	Peptidoglycan recognition protein SC1a	PGRP-SC1a
35862	Peptidoglycan recognition protein SC2	PGRP-SC2
35886	Phosphoglucose isomerase	Pgi	Parkinson's disease acute lymphoblastic leukemia acute myeloid leukemia congenital hemolytic anemia congenital nonspherocytic hemolytic anemia heart disease intellectual disability neuromuscular disease
36060	Phosphofructokinase	Pfk	disease of metabolism glycogen storage disease VII glycogen storage disease
36079	Chondroitin sulfate N-acetylgalactosaminyltransferase	Csgalnact
36279	beta1,3-galactosyltransferase 1	GalT1
36564	O-fucosyltransferase 1	O-fut1	Dowling-Degos disease
36585	beta1,4-N-acetylgalactosaminyltransferase A	beta4GalNAcTA	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease multiple sclerosis
36614	tout-velu	ttv	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
36717	Polypeptide N-Acetylgalactosaminyltransferase 1	Pgant1	hyperphosphatemic familial tumoral calcinosis
36773	Dystroglycan	Dg	Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2P bronchopulmonary dysplasia congenital muscular dystrophy-dystroglycanopathy type A9 dilated cardiomyopathy inclusion body myositis lissencephaly muscular atrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy muscular dystrophy myocardial infarction primary biliary cholangitis type 2 diabetes mellitus
36841	Poly(ADP-ribose) polymerase 16	Parp16
36856	Dolichol kinase	Dolk	congenital disorder of glycosylation Im congenital disorder of glycosylation type I
36863	Amylase related	Amyrel

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