GlyCosmos Portal

Displaying entries **1 - 25** of **698** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology ▲
P14599	Amyloid-beta-like protein	Appl CG7727	5	0	Alzheimer's disease 1 Alzheimer's disease
O02194	Presenilin homolog	CG18803 PS Psn	1	0	Alzheimer's disease 3 Alzheimer's disease dilated cardiomyopathy early-onset Parkinson's disease
Q9VY86	TM2 domain-containing protein amaretto	CG11103 amrt	2	0	Alzheimer's disease
Q9W2H1	TM2 domain-containing protein biscotti	CG10795 bisc	3	0	Alzheimer's disease
Q9U4H5	TM2 domain-containing protein almondex	CG12127 amx	6	0	Alzheimer's disease
Q9VC27	Nicastrin	CG7012 NCSTN Nct	9	0	Alzheimer's disease
B7Z002	Kismet, isoform C	136/31 2532 5841 BEST:GM02209 CG18326 CG3660 CG3696 DmelPex20 Dmel\CG3696 Dmel_CG3696 EC2-7 EK2-4 EP(2)0474 EP474 FBtr0078144 GM02209 KIS KIS-L Kis Kismet Pex20 Su(Pc)21AB anon-WO0172774.164 anon-WO0257455.5 kis kiss l(2)07812 l(2)k08827 l(2)k11324 l(2)k13631 l(2)k14112 l(2)k16510 l(2)s3527 l(2)s4771 l(2)s4793	6	0	CHARGE syndrome autism spectrum disorder congenital heart disease
P13607	Sodium/potassium-transporting ATPase subunit alpha	Atpalpha CG5670 Na-p	1	1	Charcot-Marie-Tooth disease type 2DD epilepsy familial hemiplegic migraine nervous system disease
Q0E9H9	Cell adhesion molecule Dscam1	CG17800 Dscam Dscam1 p270	12	0	Down syndrome autism spectrum disorder
P49657	Serine/threonine-protein kinase minibrain	CG7826 mnb	2	0	Down syndrome syndromic intellectual disability
P35500	Sodium channel protein para	CG9907 para	6	0	Dravet syndrome epilepsy generalized epilepsy with febrile seizures plus 2 generalized epilepsy with febrile seizures plus
M9MRD1	Muscle-specific protein 300 kDa	CG42768 Msp300	4	0	Emery-Dreifuss muscular dystrophy
P10040	Protein crumbs	CG6383 crb	36	0	Leber congenital amaurosis retinitis pigmentosa
P20241	Neuroglian	CG1634 Nrg	9	0	MASA syndrome epilepsy
P33450	Cadherin-related tumor suppressor	CG3352 ft	38	0	Van Maldergem syndrome 2 carcinoma neurodegenerative disease obesity
Q9VTK2	Protein O-mannosyltransferase 1	CG6097 POMT1 rt	2	0	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A1 muscular dystrophy-dystroglycanopathy
Q9W5D4	Protein O-mannosyl-transferase 2	CG12311 Pomt2 tw	7	0	Walker-Warburg syndrome muscular dystrophy-dystroglycanopathy
Q8IMZ9	Wolframin	CG4917 wfs1	2	0	Wolfram syndrome 1
P07207	Neurogenic locus Notch protein	CG3936 N	69	1	adenocarcinoma alcohol use disorder brain cancer cancer central nervous system cancer colorectal cancer intestinal cancer
P09208	Insulin-like receptor	CG18402 Dir-a IR InR Inr-a	22	0	alcohol dependence cancer diabetes mellitus diabetic neuropathy glucose metabolism disease high grade glioma sleep disorder type 2 diabetes mellitus
P04412	Epidermal growth factor receptor	CG10079 DER Egfr c-erbB top	11	0	alcohol use disorder carcinoma cardiomyopathy intestinal cancer
P41596	Dopamine receptor 1	CG9652 Dop1R1 DopR DopR1 DopR35EF	5	0	alcohol use disorder depressive disorder
Q01083	Protein spitz	CG10334 spi	1	0	alcohol use disorder intestinal cancer
Q9VLL3	A-kinase anchor protein 200	Akap200 CG13388 MESR2	3	0	alcohol use disorder
P21520	Protein scabrous	CG17579 sca	6	0	alcohol use disorder

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