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 **1 - 25** of **311** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
37028	acyl-CoA oxidase 1	ACOX1	Mitchell syndrome obesity peroxisomal acyl-CoA oxidase deficiency peroxisomal disease steatotic liver disease
41104	ATPase H+ transporting accessory protein 2	ATP6AP2	X-linked parkinsonism-spasticity syndrome congenital disorder of glycosylation type II congenital disorder of glycosylation hypertension syndromic X-linked intellectual disability Hedera type syndromic X-linked intellectual disability
43183	Aldolase 1	Ald1	autoimmune disease of the nervous system borna disease hepatocellular carcinoma hereditary fructose intolerance syndrome liver benign neoplasm peritonitis type 2 diabetes mellitus
42146	ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase	Alg1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
326193	ALG10 alpha-1,2-glucosyltransferase	Alg10	long QT syndrome 2 nonsyndromic deafness
40402	ALG11, alpha-1,2-mannosyltransferase	Alg11	congenital disorder of glycosylation Ip
41191	Alg12 alpha-1,6-mannosyltransferase	Alg12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
43443	Alg13 UDP-N-acetylglucosaminyltransferase subunit	Alg13
32479	ALG14, UDP-N-acetylglucosaminyltransferase subunit	Alg14	congenital myasthenic syndrome 15
38374	ALG2, alpha-1,3/1,6-mannosyltransferase	Alg2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
37754	ALG3, alpha-1,3- mannosyltransferase	Alg3	congenital disorder of glycosylation Id congenital disorder of glycosylation
34711	Alg7 dolichyl-phosphate N-acetylglucosaminephosphotransferase	Alg7	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
43031	ALG9, alpha-1,2-mannosyltransferase	Alg9	congenital disorder of glycosylation Il congenital disorder of glycosylation type I
36932	Amylase distal	Amy-d
47764	Amylase proximal	Amy-p
36863	Amylase related	Amyrel
48224	Adenine phosphoribosyltransferase	Aprt	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
43565	Axin	Axn	Parkinson's disease cancer colon adenoma colon cancer colon carcinoma colorectal cancer colorectal carcinoma congenital heart disease craniosynostosis dilated cardiomyopathy endometrial adenocarcinoma esophagus squamous cell carcinoma familial adenomatous polyposis gallbladder cancer hepatoblastoma hepatocellular carcinoma liver cirrhosis lung adenocarcinoma lung cancer lung non-small cell carcinoma lung small cell carcinoma oral mucosa leukoplakia oral squamous cell carcinoma orofacial cleft transient cerebral ischemia urinary bladder cancer
34215	Core 1 Galactosyltransferase A	C1GalTA	autoimmune disease of blood
43394	uncharacterized protein	CG10000
33800	uncharacterized protein	CG11149
38561	uncharacterized protein	CG11357
38249	uncharacterized protein	CG13937
33760	uncharacterized protein	CG14024
43689	uncharacterized protein	CG1544	2-aminoadipic 2-oxoadipic aciduria Charcot-Marie-Tooth disease axonal type 2Q

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