GlyCosmos Portal

Displaying entries **13151 - 13175** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
O76000	Putative olfactory receptor 2B3	OR2B3 OR2B3P	1	0
A0A7D9FXB9	MHC class I antigen	HLA-B	1	0
P47710	Alpha-S1-casein	CSN1S1 CASA CSN1	1	93
F6KS12	MHC class I antigen (Fragment)	HLA-C	1	0
Q9H147	Deoxynucleotidyltransferase terminal-interacting protein 1	DNTTIP1 C20orf167 TDIF1	1	1
D5FHY6	MHC class I antigen (Fragment)	HLA-B	1	0
Q96N67	Dedicator of cytokinesis protein 7	DOCK7 KIAA1771	1	1
G1EQJ4	MHC class I antigen (Fragment)	HLA-C	1	0
F8SKW5	MHC class I antigen (Fragment)	HLA-B	1	0
E2D5S1	MHC class I antigen (Fragment)	HLA-C	1	0
Q9BVV8	Protein FAM174C	FAM174C C19orf24	1	0
A0A0A7C4S1	MHC class I antigen (Fragment)	HLA-B	1	0
Q9NR21	Protein mono-ADP-ribosyltransferase PARP11	PARP11 C12orf6	1	2	microcephaly viral infectious disease
A0A0S4T3H1	MHC class I antigen	HLA-C	1	0
G1EQM3	MHC class I antigen (Fragment)	HLA-C	1	0
Q9UBV7	Beta-1,4-galactosyltransferase 7	B4GALT7 XGALT1	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
G1ENS1	MHC class I antigen (Fragment)	HLA-C	1	0
P51570	Galactokinase	GALK1 GALK	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
Q6P1K2	Polyamine-modulated factor 1	PMF1	1	1
H0YC56	Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B (Fragment)	MGAT4B	1	0
M0R1Q1	Complement C3 (Fragment)	C3	1	0
X6R8A1	Carboxypeptidase	CTSA	1	0
A0A5A2	T cell receptor beta variable 5-8	TRBV5-8 TCRBV5S4A2T	1	0
A0A7S4ZDQ1	dipeptidyl-peptidase IV (Fragment)	dpp4	1	0
A0A1U5VZM2	MHC class I antigen	HLA C	1	0

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