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 **276 - 300** of **311** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
44543	encore	enc
250735	fused lobes	fdl	Sandhoff disease Tay-Sachs disease lysosomal storage disease spinal muscular atrophy
40314	fringe	fng	spondylocostal dysostosis 3
39943	fringe connection	frc	schneckenbecken dysplasia
32162	furrowed	fw	COVID-19 schizophrenia
33162	galectin	galectin
42571	gliolectin	glec
34409	garnysstan	gny	congenital disorder of glycosylation Ic congenital disorder of glycosylation type I
31579	knockdown	kdn	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
45884	krotzkopf verkehrt	kkv
53550	lectin-24Db	lectin-24Db
3346222	lectin-37Da	lectin-37Da
3346221	lectin-37Db	lectin-37Db
42510	medial glomeruli	meigo
40981	neuronally altered carbohydrate	nac	congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc
38288	peptide O-xylosyltransferase	oxt	Desbuquois dysplasia kidney disease polycystic kidney disease pseudoxanthoma elasticum type 1 diabetes mellitus
40104	pipe	pip	attention deficit hyperactivity disorder
42493	rudimentary-like	r-l	orotic aciduria purine-pyrimidine metabolic disorder
39297	rotated abdomen	rt	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2K cardiomyopathy cleft lip congenital muscular dystrophy-dystroglycanopathy type A1 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy muscular dystrophy
326122	rumi	rumi	Dowling-Degos disease autosomal recessive limb-girdle muscular dystrophy type 2Z autosomal recessive limb-girdle muscular dystrophy
38973	sepia	se	Alzheimer's disease Parkinson's disease asthma
33734	senju	senju
38736	sulfateless	sfl	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
31248	shaggy	sgg	Alzheimer's disease Parkinson's disease Parkinsonism acute myocardial infarction amyotrophic lateral sclerosis bipolar disorder colon cancer colorectal adenocarcinoma degenerative disc disease depressive disorder diabetic encephalopathy endometrial carcinoma heart disease hypertension middle cerebral artery infarction myocardial infarction oral squamous cell carcinoma schizophrenia sciatic neuropathy status epilepticus substance-related disorder type 2 diabetes mellitus vascular dementia
38760	sugarless	sgl	developmental and epileptic encephalopathy 84

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