GlyCosmos Portal

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GlyConnect	April 19, 2023
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Displaying entries **14251 - 14275** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism ▼	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P54278	Mismatch repair endonuclease PMS2	PMS2 PMSL2	Homo sapiens (human)	0	1
O43353	Receptor-interacting serine/threonine-protein kinase 2	RIPK2 CARDIAK RICK RIP2	Homo sapiens (human)	0	1
A0A0S4T3H1	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
Q9BY19	Membrane-spanning 4-domains subfamily A member 8	MS4A8 4SPAN4 MS4A8B	Homo sapiens (human)	2	1
Q7Z442	Polycystin-1-like protein 2	PKD1L2 KIAA1879 PC1L2	Homo sapiens (human)	10	1	Meckel syndrome autosomal dominant polycystic kidney disease colorectal cancer colorectal carcinoma familial periodic paralysis hypoplastic left heart syndrome large intestine cancer myopathy neuromuscular disease
G1EQM3	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9UBV7	Beta-1,4-galactosyltransferase 7	B4GALT7 XGALT1	Homo sapiens (human)	1	0	Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome Hailey-Hailey disease IgA glomerulonephritis Laron syndrome Larsen-like syndrome B3GAT3 type Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Rothmund-Thomson syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome achondroplasia aortic valve disease 2 aortic valve stenosis arthritis arthropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive Robinow syndrome autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bone disease cartilage disease chondrodysplasia-pseudohermaphroditism syndrome cleidocranial dysplasia clubfoot colitis collagen disease coloboma congenital disorder of glycosylation type IId congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 connective tissue disease cryptorchidism cutis laxa enophthalmos gastroenteritis gingivitis hepatocellular carcinoma humeroradial synostosis ileitis ileocolitis lipoatrophic diabetes mellitus lipodystrophy liver cancer mal de Meleda microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II mucopolysaccharidosis IV multiple epiphyseal dysplasia obsolete exophthalmos orbital disease osteoarthritis osteochondrodysplasia osteogenesis imperfecta pulmonary valve stenosis radioulnar synostosis restrictive dermopathy rheumatoid arthritis scoliosis skin disease spermatic cord torsion trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
Q9UN76	Sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)	SLC6A14	Homo sapiens (human)	8	3
Q9BRX9	WD repeat domain-containing protein 83	WDR83 MORG1	Homo sapiens (human)	0	1
G1ENS1	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P57740	Nuclear pore complex protein Nup107	NUP107	Homo sapiens (human)	8	2
Q14493	Histone RNA hairpin-binding protein	SLBP HBP	Homo sapiens (human)	0	1
Q9P2D8	Protein unc-79 homolog	UNC79 KIAA1409	Homo sapiens (human)	2	1
P51570	Galactokinase	GALK1 GALK	Homo sapiens (human)	1	1	cancer cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract classic galactosemia colorectal cancer colorectal carcinoma cutaneous fibrous histiocytoma cystinuria diabetic cataract disease of metabolism epidermolysis bullosa simplex localized type epidermolysis bullosa simplex galactokinase deficiency galactose epimerase deficiency galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease hepatocellular carcinoma hidradenoma inherited metabolic disorder junctional epidermolysis bullosa non-Herlitz type junctional epidermolysis bullosa with pyloric atresia junctional epidermolysis bullosa large intestine cancer liver cancer placental insufficiency senile cataract skin papilloma skin tag syringoma
Q06187	Tyrosine-protein kinase BTK	BTK AGMX1 ATK BPK	Homo sapiens (human)	0	1
Q96HC4	PDZ and LIM domain protein 5	PDLIM5 ENH	Homo sapiens (human)	30	4
O94916	Nuclear factor of activated T-cells 5	NFAT5 KIAA0827 TONEBP	Homo sapiens (human)	0	1
Q6P1K2	Polyamine-modulated factor 1	PMF1	Homo sapiens (human)	1	1
H0YC56	Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B (Fragment)	MGAT4B	Homo sapiens (human)	1	0
M0R1Q1	Complement C3 (Fragment)	C3	Homo sapiens (human)	1	0
Q8NG85	Olfactory receptor 2L3	OR2L3	Homo sapiens (human)	2	0
O43506	Disintegrin and metalloproteinase domain-containing protein 20	ADAM20	Homo sapiens (human)	6	0
X6R8A1	Carboxypeptidase	CTSA	Homo sapiens (human)	1	0
P0C1H6	Histone H2B type F-M	H2BW2 H2BFM	Homo sapiens (human)	0	1
P60866	Small ribosomal subunit protein uS10	RPS20	Homo sapiens (human)	0	1

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