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 **201 - 225** of **311** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
40055	UDP-glucose-glycoprotein glucosyltransferase	Uggt
40079	UDP-glycosyltransferase family 316 member A1	Ugt316A1	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer type 1 diabetes mellitus type 2 diabetes mellitus
40104	pipe	pip	attention deficit hyperactivity disorder
40314	fringe	fng	spondylocostal dysostosis 3
40402	ALG11, alpha-1,2-mannosyltransferase	Alg11	congenital disorder of glycosylation Ip
40442	Chitin synthase 2	Chs2
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
40875	Glucose dehydrogenase	Gld
40935	Phosphoribosylamidotransferase	Prat	hepatocellular carcinoma renal cell carcinoma
40981	neuronally altered carbohydrate	nac	congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc
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
41126	alpha-Mannosidase class II a	alpha-Man-IIa	congenital dyserythropoietic anemia schizophrenia systemic lupus erythematosus
41166	Calreticulin	Calr	Burkitt lymphoma Parkinson's disease acute myeloid leukemia colon cancer colon carcinoma colorectal cancer esophagus squamous cell carcinoma essential thrombocythemia gallbladder cancer hepatocellular carcinoma lung adenocarcinoma lung cancer lung non-small cell carcinoma myelofibrosis nasopharynx carcinoma neuroendocrine tumor oral squamous cell carcinoma ovarian cancer pancreatic ductal adenocarcinoma pancreatic ductal carcinoma sideroblastic anemia stomach cancer thrombocytosis vitamin B12 deficiency
41191	Alg12 alpha-1,6-mannosyltransferase	Alg12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
41334	UDP-glycosyltransferase family 35 member A1	Ugt35A1	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer type 1 diabetes mellitus type 2 diabetes mellitus
41379	Peptidoglycan recognition protein LB	PGRP-LB
41528	N-acetylneuraminic acid synthase	NANS	spondyloepimetaphyseal dysplasia, Genevieve-type
41573	UDP-glycosyltransferase family 37 member A2	Ugt37A2	Crigler-Najjar syndrome bilirubin metabolic disorder hyperthyroidism type 1 diabetes mellitus type 2 diabetes mellitus
41574	UDP-glycosyltransferase family 37 member A3	Ugt37A3	Crigler-Najjar syndrome Crohn's disease Gilbert syndrome alcoholic pancreatitis bilirubin metabolic disorder breast cancer cholangiocarcinoma cholecystolithiasis cholelithiasis endometrial cancer hepatitis B hyperthyroidism lung non-small cell carcinoma myeloid leukemia ovarian cancer pancreatic cancer type 1 diabetes mellitus type 2 diabetes mellitus
41823	Glycogen synthase	Glys	Lafora disease cardiovascular system disease glycogen storage disease
41867	Transmembrane O-mannosyltransferase targeting cadherins 4	Tmtc4	autosomal recessive nonsyndromic deafness
41913	alpha-Mannosidase class II b	alpha-Man-IIb
42115	slalom	sll	hypomyelinating leukodystrophy 26
42146	ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase	Alg1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
42254	Phosphatidylglycerophosphate synthase 1	PGS1

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