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 **876 - 900** of **919** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
31591	uncharacterized protein	CG34417
31579	knockdown	kdn	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
31574	uncharacterized protein	CG15894
31553	ER GDP-fucose transporter	Efr
31551	vanin-like	vanin-like
31547	Neprilysin 1	Nep1
31541	uncharacterized protein	CG4666
31517	Glycosylphosphatidylinositol anchor attachment 1	GAA1
31487	Post-GPI attachment to proteins 1	PGAP1	holoprosencephaly
31480	Sirtuin 4	Sirt4	metabolic dysfunction-associated steatotic liver disease
31457	Nutrient Amino Acid Transporter 1	NAAT1
31399	torsin	Torsin
31380	uncharacterized protein	CG3556
31364	Fasciclin 2	Fas2
31363	twenty-four	tyf
31358	brainiac	brn	pancreatic cancer
31329	Poly(ADP-ribose) glycohydrolase	Parg	borna disease brain infarction stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
31322	Dpr-interacting protein alpha	DIP-alpha
31309	dunce	dnc
31293	Notch	N	Adams-Oliver syndrome Alagille syndrome Alzheimer's disease CADASIL 1 Hajdu-Cheney syndrome adenocarcinoma adult T-cell leukemia/lymphoma alcohol use disorder aortic valve disease 1 brain cancer cancer central nervous system cancer cholangiocarcinoma colorectal cancer congenital heart disease endometrial cancer hemangiopericytoma infantile myofibromatosis intestinal cancer lateral meningocele syndrome lung adenocarcinoma lung large cell carcinoma lung small cell carcinoma multiple myeloma obesity pre-eclampsia pulmonary fibrosis retinopathy of prematurity transient cerebral ischemia
31292	kin of irre	kirre
31290	roughest	rst
31271	white	w
31270	uncharacterized protein	CG32795
31255	UDP-galactose transporter	Ugalt	bacterial infectious disease congenital disorder of glycosylation type IIm