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 **151 - 175** of **311** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
37950	Sialyltransferase	SiaT	alcohol use disorder high grade glioma
38076	UDP-galactose 4'-epimerase	Gale	galactose epimerase deficiency galactosemia thrombocytopenia
38106	uncharacterized protein	CG34056
38122	Lysozyme X	LysX	familial visceral amyloidosis
38125	Lysozyme B	LysB	familial visceral amyloidosis
38127	Lysozyme D	LysD	familial visceral amyloidosis
38128	Lysozyme E	LysE	familial visceral amyloidosis
38129	Lysozyme P	LysP	familial visceral amyloidosis
38130	Lysozyme S	LysS	familial visceral amyloidosis
38164	alpha1,3-fucosyltransferase D	FucTD
38223	Chitinase 2	Cht2	asthma cryptococcosis silicosis sinusitis
38249	uncharacterized protein	CG13937
38288	peptide O-xylosyltransferase	oxt	Desbuquois dysplasia kidney disease polycystic kidney disease pseudoxanthoma elasticum type 1 diabetes mellitus
38346	Polypeptide N-Acetylgalactosaminyltransferase 6	Pgant6
38355	Carnitine palmitoyltransferase 2	CPT2	brain disease lipid metabolism disorder muscular disease
38374	ALG2, alpha-1,3/1,6-mannosyltransferase	Alg2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
38446	Phosphatidylinositol glycan anchor biosynthesis class B	PIG-B	developmental and epileptic encephalopathy 80 sleeping sickness
38528	Hexosaminidase 1	Hexo1	Sandhoff disease Tay-Sachs disease lysosomal storage disease spinal muscular atrophy
38561	uncharacterized protein	CG11357
38736	sulfateless	sfl	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
38760	sugarless	sgl	developmental and epileptic encephalopathy 84
38858	Peptidoglycan recognition protein SD	PGRP-SD
38895	Sterile alpha and Armadillo motif	Sarm	amyotrophic lateral sclerosis neurodegenerative disease
38973	sepia	se	Alzheimer's disease Parkinson's disease asthma
39013	division abnormally delayed	dally	Simpson-Golabi-Behmel syndrome type 1 atypical teratoid rhabdoid tumor hepatoblastoma hepatocellular carcinoma liver cirrhosis nephroblastoma placental site trophoblastic tumor