GlyCosmos Portal

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Displaying entries **125501 - 125525** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q3UH93	Plexin-D1	Plxnd1	Mus musculus (house mouse)	14	12
P30825	High affinity cationic amino acid transporter 1	SLC7A1 ATRC1 ERR REC1L	Homo sapiens (human)	2	12
P78423	Fractalkine	CX3CL1 FKN NTT SCYD1	Homo sapiens (human)	13	12
Q13586	Stromal interaction molecule 1	STIM1 GOK	Homo sapiens (human)	8	12
Q60841	Reelin	Reln Rl	Mus musculus (house mouse)	20	12
P14923	Junction plakoglobin	JUP CTNNG DP3	Homo sapiens (human)	6	12
Q8C419	Metabotropic glycine receptor	Gpr158 Kiaa1136	Mus musculus (house mouse)	7	12
Q15758	Neutral amino acid transporter B(0)	SLC1A5 ASCT2 M7V1 RDR RDRC	Homo sapiens (human)	2	12
P37173	TGF-beta receptor type-2	TGFBR2	Homo sapiens (human)	7	12
P51688	N-sulphoglucosamine sulphohydrolase	SGSH HSS	Homo sapiens (human)	6	12	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Balo concentric sclerosis Kearns-Sayre syndrome Kluver-Bucy syndrome Pick's disease Reye syndrome Schwartz-Jampel syndrome 1 Stevens-Johnson syndrome adrenoleukodystrophy ankylosing spondylitis anorexia nervosa arthritis arthropathy beta-mannosidosis cancer cardiomyopathy central nervous system disease central nervous system origin vertigo cerebral degeneration chronic obstructive pulmonary disease cone-rod dystrophy congenital nystagmus depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea dissociated nystagmus embryoma endomyocardial fibrosis eosinophilic esophagitis epilepsy fundus albipunctatus fundus dystrophy hypertrichosis hypertrophic cardiomyopathy 1 hypertrophic cardiomyopathy intellectual disability learning disability lingual-facial-buccal dyskinesia lysosomal storage disease major depressive disorder melancholic depression movement disease mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis mucosulfatidosis multiple epiphyseal dysplasia narcolepsy nervous system disease neurodegeneration with brain iron accumulation neurodegenerative disease obsolete melancholia osteoarthritis osteochondrodysplasia pathologic nystagmus retinitis pigmentosa sensorineural hearing loss spontaneous ocular nystagmus visual epilepsy
Q80TS3	Adhesion G protein-coupled receptor L3	Adgrl3 Kiaa0768 Lec3 Lphn3	Mus musculus (house mouse)	11	12
Q9Z2W9	Glutamate receptor 3	Gria3 GluA3 Glur3 Kiaa4184	Mus musculus (house mouse)	6	12
Q9JIS5	Synaptic vesicle glycoprotein 2A	Sv2a Kiaa0736 Sv2	Mus musculus (house mouse)	3	12
P56528	ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1	Cd38	Mus musculus (house mouse)	4	12
Q969V3	BOS complex subunit NCLN	NCLN	Homo sapiens (human)	4	12
Q9JLC4	VPS10 domain-containing receptor SorCS1	Sorcs1 Sorcs	Mus musculus (house mouse)	12	12
Q6UXG2	Endosome/lysosome-associated apoptosis and autophagy regulator 1	ELAPOR1 EIG121 KIAA1324	Homo sapiens (human)	8	12
P00724	Invertase 2	SUC2	Saccharomyces cerevisiae S288C	13	12
Q6NSJ0	Myogenesis-regulating glycosidase	MYORG KIAA1161	Homo sapiens (human)	6	12	amnestic disorder basal ganglia calcification choreatic disease dystonia epilepsy hydrocephalus lingual-facial-buccal dyskinesia microcephaly migraine neurodegenerative disease placental insufficiency recurrent corneal erosion retrograde amnesia secondary Parkinson disease syndromic X-linked intellectual disability type 10 thrombocytopenia visual epilepsy
Q53RD9	Fibulin-7	FBLN7 TM14	Homo sapiens (human)	6	12
Q68FM6	Protein phosphatase 1 regulatory subunit 29	Elfn2 Kiaa1904 Lrrc62 Ppp1r29	Mus musculus (house mouse)	7	12
Q9H173	Nucleotide exchange factor SIL1	SIL1	Homo sapiens (human)	16	12
Q9Y2J2	Band 4.1-like protein 3	EPB41L3 DAL1 KIAA0987	Homo sapiens (human)	3	12
Q15155	BOS complex subunit NOMO1	NOMO1 PM5	Homo sapiens (human)	6	12
Q16787	Laminin subunit alpha-3	LAMA3 LAMNA	Homo sapiens (human)	18	12

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