GlyCosmos Portal

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UniProt ID ▲	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9UBQ6	Exostosin-like 2	EXTL2 EXTR2	1	0	autosomal dominant osteopetrosis 2 autosomal recessive osteopetrosis 7 cancer chronic kidney disease hereditary multiple exostoses mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIC mucopolysaccharidosis osteopetrosis osteosclerosis
Q9UBQ7	Glyoxylate reductase/hydroxypyruvate reductase	GRHPR GLXR	1	1	atypical hemolytic-uremic syndrome calcinosis calcium metabolism disease chronic kidney disease hemolytic-uremic syndrome hypercalcemia kidney failure nephrocalcinosis nephrolithiasis phosphorus metabolism disease primary hyperoxaluria prostate cancer prostate carcinoma ureteral obstruction uric acid nephrolithiasis urinary tract obstruction
Q9UBR2	Cathepsin Z	CTSZ	2	21
Q9UBS4	DnaJ homolog subfamily B member 11	DNAJB11 EDJ ERJ3 HDJ9	3	11
Q9UBS5	Gamma-aminobutyric acid type B receptor subunit 1	GABBR1 GPRC3A	7	0
Q9UBS8	E3 ubiquitin-protein ligase RNF14	RNF14 ARA54	0	1
Q9UBS9	SUN domain-containing ossification factor	SUCO C1orf9 CH1 OPT SLP1	14	15
Q9UBT2	SUMO-activating enzyme subunit 2	UBA2 SAE2 UBLE1B	0	1
Q9UBT3	Dickkopf-related protein 4	DKK4	0	1
Q9UBT6	DNA polymerase kappa	POLK DINB1	0	1
Q9UBT7	Alpha-catulin	CTNNAL1	1	1
Q9UBU2	Dickkopf-related protein 2	DKK2	1	0
Q9UBU6	Protein FAM8A1	FAM8A1 AHCP	0	1
Q9UBU7	Protein DBF4 homolog A	DBF4 ASK DBF4A ZDBF1	4	1
Q9UBU8	Mortality factor 4-like protein 1	MORF4L1 MRG15	0	1
Q9UBU9	Nuclear RNA export factor 1	NXF1 TAP	2	1
Q9UBV2	Protein sel-1 homolog 1	SEL1L TSA305	14	47
Q9UBV4	Protein Wnt-16	WNT16	3	1
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
Q9UBV8	Peflin	PEF1 ABP32	0	1
Q9UBW7	Zinc finger MYM-type protein 2	ZMYM2 FIM RAMP ZNF198	2	2
Q9UBW8	COP9 signalosome complex subunit 7a	COPS7A CSN7A DERP10	0	1
Q9UBX1	Cathepsin F	CTSF	5	21
Q9UBX5	Fibulin-5	FBLN5 DANCE	7	85
Q9UBX7	Kallikrein-11	KLK11 PRSS20 TLSP	4	3

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