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 **76 - 100** of **311** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
43005	Catalytic subunit 3B of the oligosaccharyltransferase complex	Stt3B	congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix
42991	beta-4-galactosyltransferase 7	beta4GalT7	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
42761	Ribosomal protein S3	RpS3	intrinsic cardiomyopathy
42698	uncharacterized protein	CG31139	Dowling-Degos disease autosomal recessive limb-girdle muscular dystrophy type 2Z
42620	Pyruvate kinase	PyK	Gaucher's disease congenital nonspherocytic hemolytic anemia disease of metabolism hyperglycemia hypertension malaria metabolic dysfunction-associated steatotic liver disease pyruvate kinase deficiency of red cells type 2 diabetes mellitus
42571	gliolectin	glec
42538	UDP-glycosyltransferase family 49 member B2	Ugt49B2	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
42518	O-GlcNAcase	Oga	type 2 diabetes mellitus
42510	medial glomeruli	meigo
42493	rudimentary-like	r-l	orotic aciduria purine-pyrimidine metabolic disorder
42380	Heparan sulfate 6-O-sulfotransferase	Hs6st	Paganini-Miozzo syndrome hypogonadotropic hypogonadism 15 with or without anosmia
42254	Phosphatidylglycerophosphate synthase 1	PGS1
42146	ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase	Alg1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
42115	slalom	sll	hypomyelinating leukodystrophy 26
41913	alpha-Mannosidase class II b	alpha-Man-IIb
41867	Transmembrane O-mannosyltransferase targeting cadherins 4	Tmtc4	autosomal recessive nonsyndromic deafness
41823	Glycogen synthase	Glys	Lafora disease cardiovascular system disease glycogen storage disease
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
41573	UDP-glycosyltransferase family 37 member A2	Ugt37A2	Crigler-Najjar syndrome bilirubin metabolic disorder hyperthyroidism type 1 diabetes mellitus type 2 diabetes mellitus
41528	N-acetylneuraminic acid synthase	NANS	spondyloepimetaphyseal dysplasia, Genevieve-type
41379	Peptidoglycan recognition protein LB	PGRP-LB
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
41191	Alg12 alpha-1,6-mannosyltransferase	Alg12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
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
41126	alpha-Mannosidase class II a	alpha-Man-IIa	congenital dyserythropoietic anemia schizophrenia systemic lupus erythematosus

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