GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
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The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **6726 - 6750** 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
Q9UE02	MICA protein (Fragment)	MICA	Homo sapiens (human)	2	0
Q9UE01	MICA protein (Fragment)	MICA	Homo sapiens (human)	3	0
Q9UE00	MICA protein (Fragment)	MICA	Homo sapiens (human)	3	0
Q9UDZ9	MICA protein (Fragment)	MICA	Homo sapiens (human)	3	0
Q9UDZ8	MICA protein (Fragment)	MICA	Homo sapiens (human)	3	0
Q9UDY8	Mucosa-associated lymphoid tissue lymphoma translocation protein 1	MALT1 MLT	Homo sapiens (human)	1	1
Q9UDY4	DnaJ homolog subfamily B member 4	DNAJB4 DNAJW HLJ1	Homo sapiens (human)	0	1
Q9UDY2	Tight junction protein ZO-2	TJP2 X104 ZO2	Homo sapiens (human)	3	3
Q9UDX3	SEC14-like protein 4	SEC14L4 TAP3	Homo sapiens (human)	0	1
Q9UDW1	Cytochrome b-c1 complex subunit 9	UQCR10 UCRC	Homo sapiens (human)	0	1
Q9UC06	Zinc finger protein 70	ZNF70	Homo sapiens (human)	0	1
Q9UBZ9	DNA repair protein REV1	REV1 REV1L	Homo sapiens (human)	0	1
Q9UBY5	Lysophosphatidic acid receptor 3	LPAR3 EDG7 LPA3	Homo sapiens (human)	2	0
Q9UBY0	Sodium/hydrogen exchanger 2	SLC9A2 NHE2	Homo sapiens (human)	2	1
Q9UBX8	Beta-1,4-galactosyltransferase 6	B4GALT6	Homo sapiens (human)	8	1	colorectal cancer colorectal carcinoma large intestine cancer multiple sclerosis skin disease
Q9UBX7	Kallikrein-11	KLK11 PRSS20 TLSP	Homo sapiens (human)	4	3
Q9UBX5	Fibulin-5	FBLN5 DANCE	Homo sapiens (human)	7	85
Q9UBX1	Cathepsin F	CTSF	Homo sapiens (human)	5	21
Q9UBW8	COP9 signalosome complex subunit 7a	COPS7A CSN7A DERP10	Homo sapiens (human)	0	1
Q9UBW7	Zinc finger MYM-type protein 2	ZMYM2 FIM RAMP ZNF198	Homo sapiens (human)	2	2
Q9UBV8	Peflin	PEF1 ABP32	Homo sapiens (human)	0	1
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
Q9UBV4	Protein Wnt-16	WNT16	Homo sapiens (human)	3	1
Q9UBV2	Protein sel-1 homolog 1	SEL1L TSA305	Homo sapiens (human)	14	47
Q9UBU9	Nuclear RNA export factor 1	NXF1 TAP	Homo sapiens (human)	2	1

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