GlyCosmos Portal

Displaying entries **16576 - 16600** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	Disease Ontology
A0A7D9FXB9	MHC class I antigen	HLA-B	1
P59540	Taste receptor type 2 member 46	TAS2R46	2
F6KS12	MHC class I antigen (Fragment)	HLA-C	1
D5FHY6	MHC class I antigen (Fragment)	HLA-B	1
Q9Y5Y4	Prostaglandin D2 receptor 2	PTGDR2 CRTH2 DL1R GPR44	2
G1EQJ4	MHC class I antigen (Fragment)	HLA-C	1
F8SKW5	MHC class I antigen (Fragment)	HLA-B	1
E2D5S1	MHC class I antigen (Fragment)	HLA-C	1
Q9BVV8	Protein FAM174C	FAM174C C19orf24	1
A0A0A7C4S1	MHC class I antigen (Fragment)	HLA-B	1
A0A0S4T3H1	MHC class I antigen	HLA-C	1
G1EQM3	MHC class I antigen (Fragment)	HLA-C	1
Q9UBV7	Beta-1,4-galactosyltransferase 7	B4GALT7 XGALT1	1	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
G1ENS1	MHC class I antigen (Fragment)	HLA-C	1
H0YC56	Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B (Fragment)	MGAT4B	1
M0R1Q1	Complement C3 (Fragment)	C3	1
Q8NG85	Olfactory receptor 2L3	OR2L3	2
O43506	Disintegrin and metalloproteinase domain-containing protein 20	ADAM20	6
X6R8A1	Carboxypeptidase	CTSA	1
A0A5A2	T cell receptor beta variable 5-8	TRBV5-8 TCRBV5S4A2T	1
A0A7S4ZDQ1	dipeptidyl-peptidase IV (Fragment)	dpp4	1
A0A1U5VZM2	MHC class I antigen	HLA C	1
G1ENP0	MHC class I antigen (Fragment)	HLA-C	1
P49788	Retinoic acid receptor responder protein 1	RARRES1 PEIG1 TIG1	2
G5DSS2	MHC class I antigen	HLA-B	1

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