GlyCosmos Portal

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Displaying entries **123276 - 123300** 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
Q8BXR9	Oxysterol-binding protein-related protein 6	Osbpl6	Mus musculus (house mouse)	3	3
Q03188	Centromere protein C	CENPC CENPC1 ICEN7	Homo sapiens (human)	4	3
Q8WWI1	LIM domain only protein 7	LMO7 FBX20 FBXO20 KIAA0858	Homo sapiens (human)	41	3
Q13617	Cullin-2	CUL2	Homo sapiens (human)	2	3
Q0ZGT2	Nexilin	NEXN	Homo sapiens (human)	2	3
Q96T58	Msx2-interacting protein	SPEN KIAA0929 MINT SHARP	Homo sapiens (human)	73	3
Q03350	Thrombospondin-2	Thbs2 Tsp2	Mus musculus (house mouse)	7	3
P29120	Neuroendocrine convertase 1	PCSK1 NEC1	Homo sapiens (human)	6	3
Q8C166	Copine-1	Cpne1	Mus musculus (house mouse)	2	3
Q5F2E7	FMR1-interacting protein NUFIP2	Nufip2 Kiaa1321	Mus musculus (house mouse)	14	3
E9Q7T7	Chondroadherin-like protein	Chadl SLRR4B	Mus musculus (house mouse)	3	3
Q8BMG7	Rab3 GTPase-activating protein non-catalytic subunit	Rab3gap2 Kiaa0839	Mus musculus (house mouse)	2	3
P14410	Sucrase-isomaltase, intestinal	SI	Homo sapiens (human)	18	3	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 Barrett's esophagus Clostridium difficile colitis Duchenne muscular dystrophy Fabry disease Gaucher's disease Gerstmann-Straussler-Scheinker syndrome Gorham's disease Japanese encephalitis Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Richter's syndrome adenocarcinoma adenoma amyotrophic lateral sclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy brachydactyly type C brachydactyly cancer cardiomyopathy cardiovascular system disease cerebral degeneration chronic lymphocytic leukemia chylomicron retention disease colitis colorectal cancer colorectal carcinoma congenital disorder of glycosylation congenital muscular dystrophy coronary artery disease cribriform carcinoma cystic fibrosis cystinuria dengue disease depressive disorder diabetes mellitus diabetic ketoacidosis diarrhea disease of metabolism distal myopathy embryoma endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hypertrophic cardiomyopathy familial periodic paralysis galactosemia gastric cardia adenocarcinoma gastroenteritis gastrointestinal system disease glucose intolerance glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease granular cell carcinoma heart disease hyperglycemia hypertrophic cardiomyopathy hypoglycemia ileitis ileocolitis intestinal disease irritable bowel syndrome kwashiorkor lactose intolerance large intestine cancer limb-girdle muscular dystrophy lipid storage disease lysosomal storage disease major depressive disorder marasmus melancholic depression muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myotonic dystrophy type 1 myotonic dystrophy type 2 nephrolithiasis neurocirculatory asthenia neurodegenerative disease nutmeg liver nutrition disease obesity obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete melancholia oculopharyngeal muscular dystrophy peptic ulcer disease prediabetes syndrome progressive muscular atrophy prolactinoma protein-energy malnutrition punctate palmoplantar keratoderma type III rippling muscle disease 2 sudden infant death syndrome tropical sprue tubular adenocarcinoma type 2 diabetes mellitus uric acid nephrolithiasis viral infectious disease yellow fever
P14733	Lamin-B1	Lmnb1	Mus musculus (house mouse)	4	3
Q60932	Voltage-dependent anion-selective channel protein 1	Vdac1 Vdac5	Mus musculus (house mouse)	5	3
P30556	Type-1 angiotensin II receptor	AGTR1 AGTR1A AGTR1B AT2R1 AT2R1B	Homo sapiens (human)	3	3
P51660	Peroxisomal multifunctional enzyme type 2	Hsd17b4 Edh17b4	Mus musculus (house mouse)	2	3
Q8BNE1	TRPM8 channel-associated factor 1	Tcaf1 Fam115a Kiaa0738	Mus musculus (house mouse)	3	3
P22004	Bone morphogenetic protein 6	BMP6 VGR	Homo sapiens (human)	7	3
E9Q616	AHNAK nucleoprotein (desmoyokin)	Ahnak	Mus musculus (house mouse)	7	3
Q8WYB5	Histone acetyltransferase KAT6B	KAT6B KIAA0383 MORF MOZ2 MYST4	Homo sapiens (human)	5	3
O88792	Junctional adhesion molecule A	F11r Jam1 Jcam Jcam1	Mus musculus (house mouse)	2	3
P16519	Neuroendocrine convertase 2	PCSK2 NEC2	Homo sapiens (human)	3	3
Q92945	Far upstream element-binding protein 2	KHSRP FUBP2	Homo sapiens (human)	9	3
Q9R1V4	Disintegrin and metalloproteinase domain-containing protein 11	Adam11 Mdc	Mus musculus (house mouse)	5	3

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