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 **26 - 50** of **311** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
3355116	Chitinase 10	Cht10	asthma cryptococcosis hypertension silicosis sinusitis
38223	Chitinase 2	Cht2	asthma cryptococcosis silicosis sinusitis
32259	Chondroitin polymerizing factor	Chpf
36079	Chondroitin sulfate N-acetylgalactosaminyltransferase	Csgalnact
32497	Chondroitin sulfate synthase	Chsy	temtamy preaxial brachydactyly syndrome
34215	Core 1 Galactosyltransferase A	C1GalTA	autoimmune disease of blood
34159	Defender against apoptotic cell death 1	Dad1
36856	Dolichol kinase	Dolk	congenital disorder of glycosylation Im congenital disorder of glycosylation type I
35240	Dolichyl-phosphate mannosyltransferase subunit 1	Dpm1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
8674033	Dolichyl-phosphate mannosyltransferase subunit 2	Dpm2	congenital disorder of glycosylation Iu
3885575	Dolichyl-phosphate mannosyltransferase subunit 3	Dpm3	congenital disorder of glycosylation type I muscular dystrophy-dystroglycanopathy type B15
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
33424	EGF-domain O-GlcNAc transferase	Eogt	Adams-Oliver syndrome
31553	ER GDP-fucose transporter	Efr
31154	ER degradation enhancer, mannosidase alpha-like 1	Edem1
34714	ER degradation enhancer, mannosidase alpha-like 2	Edem2	congenital disorder of glycosylation type II cystic fibrosis
33351	Enolase	Eno	Alzheimer's disease Parkinsonism aortic valve stenosis brain disease breast carcinoma hypertension migraine without aura neuroendocrine carcinoma prostate cancer toxic shock syndrome urinary bladder cancer visual epilepsy
33658	FIG4 phosphoinositide 5-phosphatase	FIG4	Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease Yunis-Varon syndrome amyotrophic lateral sclerosis type 11 bilateral parasagittal parieto-occipital polymicrogyria neurodegenerative disease
40599	GDP-mannose pyrophosphorylase B	Gmppb	autosomal recessive limb-girdle muscular dystrophy type 2T congenital muscular dystrophy-dystroglycanopathy A14 muscular dystrophy-dystroglycanopathy type B14 muscular dystrophy-dystroglycanopathy
33653	GS1-like	Gs1l
33935	Galactose-1-phosphate uridylyltransferase	Galt	classic galactosemia galactosemia
35216	Galactose-specific C-type lectin	Lectin-galC1
40875	Glucose dehydrogenase	Gld
37516	Glucosylceramide synthase	GlcT	hypertension
251900	Glucuronyltransferase I	GlcAT-I	Barrett's esophagus Larsen-like syndrome B3GAT3 type pulmonary fibrosis schizophrenia

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