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 **301 - 325** of **919** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
41397	uncharacterized protein	CG14712
41379	Peptidoglycan recognition protein LB	PGRP-LB
41369	ninaG	ninaG
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
41302	Cadherin 86C	Cad86C
41286	Tachykinin-like receptor at 86C	TkR86C
41247	Synapsin	Syn
41206	uncharacterized protein	CG8516
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
41144	blistery	by
41126	alpha-Mannosidase class II a	alpha-Man-IIa	congenital dyserythropoietic anemia schizophrenia systemic lupus erythematosus
41123	uncharacterized protein	CG8135
41119	Odorant receptor 85f	Or85f
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
41072	uncharacterized protein	CG11970
41008	Odorant receptor 85c	Or85c
41007	Odorant receptor 85b	Or85b
40991	Odorant receptor 85a	Or85a
40981	neuronally altered carbohydrate	nac	congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc
40935	Phosphoribosylamidotransferase	Prat	hepatocellular carcinoma renal cell carcinoma
40918	Serine protease 7	Sp7
40875	Glucose dehydrogenase	Gld
40861	stranded at second	sas
40859	Spindle assembly abnormal 4	Sas-4