GlyCosmos Portal

Drosophila melanogaster (fruit fly)

Summary

Taxonomy ID: 7227
PubChem Taxonomy: 7227

Genes (919) Glycans (91) Glycoproteins (697) Lectins (38) Pathways (494)

Displaying entries **1 - 25** of **919** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
37196	5-hydroxytryptamine (serotonin) receptor 1A	5-HT1A
37191	5-hydroxytryptamine (serotonin) receptor 1B	5-HT1B
32013	6-phosphogluconolactonase	Pgls
31806	8-oxoguanine DNA glycosylase	Ogg1	Graves' disease Parkinson's disease angiomyolipoma basal cell carcinoma breast cancer cataract cholangiocarcinoma coronary artery disease gestational diabetes head and neck squamous cell carcinoma hepatitis hypertension middle cerebral artery infarction ovarian cancer pancreatic cancer pre-eclampsia primary open angle glaucoma progressive supranuclear palsy prostate cancer pterygium renal cell carcinoma senile cataract status epilepticus transient cerebral ischemia transitional cell carcinoma type 2 diabetes mellitus
34170	A kinase anchor protein 200	Akap200
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
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
43031	ALG9, alpha-1,2-mannosyltransferase	Alg9	congenital disorder of glycosylation Il congenital disorder of glycosylation type I
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
33817	Accessory gland protein 26Aa	Acp26Aa
34162	Accessory gland protein 29AB	Acp29AB
40078	Accessory gland protein 76A	Acp76A
41625	Acetylcholine esterase	Ace
43826	Activin-beta	Actbeta
48224	Adenine phosphoribosyltransferase	Aprt	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
40180	Adenylyl cyclase 76E	Ac76E
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
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
34711	Alg7 dolichyl-phosphate N-acetylglucosaminephosphotransferase	Alg7	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
43671	Alkaline phosphatase 4	Alp4

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