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 **251 - 275** of **311** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
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
33653	GS1-like	Gs1l
33642	Trehalose-6-phosphate synthase 1	Tps1
33568	uncharacterized protein	CG31776
33556	Polypeptide N-Acetylgalactosaminyltransferase 2	Pgant2	congenital disorder of glycosylation type II
33512	alpha1,4-galactosyltransferase 1	alpha4GT1	pancreatic cancer
33485	uncharacterized protein	CG2983
33482	uncharacterized protein	CG18558
33481	uncharacterized protein	CG2975
33479	uncharacterized protein	CG3119
33461	Phosphoglycerate kinase	Pgk	Parkinson's disease cancer hemolytic anemia phosphoglycerate kinase 1 deficiency
33455	Transmembrane O-mannosyltransferase targeting cadherins 1	Tmtc1
33424	EGF-domain O-GlcNAc transferase	Eogt	Adams-Oliver syndrome
33386	Glycogen phosphorylase	Glyp	cholestasis glycogen storage disease V glycogen storage disease VI glycogen storage disease lactic acidosis
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
33307	tRNA-guanine transglycosylase	Tgt
33276	Transmembrane O-mannosyltransferase targeting cadherins 2	Tmtc2
33258	Post-GPI attachment to proteins 2	PGAP2	hyperphosphatasia with impaired intellectual development syndrome 3
33162	galectin	galectin
33082	Catalytic subunit 3A of the oligosaccharyltransferase complex	Stt3A	congenital disorder of glycosylation Iw
33023	Peritrophin A	Peritrophin-A
32974	Zwischenferment	Zw	Plasmodium falciparum malaria anemia cataract cerebrovascular disease cholestasis congenital hypothyroidism congenital nonspherocytic hemolytic anemia diabetes mellitus favism hemolytic anemia hepatic encephalopathy hepatocellular carcinoma hyperhomocysteinemia kidney disease malaria metabolic dysfunction-associated steatotic liver disease myocardial infarction neonatal jaundice obesity phenylketonuria renovascular hypertension transient cerebral ischemia type 1 diabetes mellitus type 2 diabetes mellitus
32918	Heparan sulfate 3-O sulfotransferase-B	Hs3st-B	colon cancer hereditary angioedema lung cancer lung non-small cell carcinoma pancreatic cancer
32896	twiggy	tgy
32854	uncharacterized protein	CG6659	spermatogenic failure 9

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