GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q9NUL3	Double-stranded RNA-binding protein Staufen homolog 2	STAU2	5	2
Q969V6	Myocardin-related transcription factor A	MRTFA KIAA1438 MAL MKL1	5	2
Q9P258	Protein RCC2	RCC2 KIAA1470 TD60	2	2
Q9Y2J4	Angiomotin-like protein 2	AMOTL2 KIAA0989	2	2
Q9GZT5	Protein Wnt-10a	WNT10A	3	2
Q96RU2	Ubiquitin carboxyl-terminal hydrolase 28	USP28 KIAA1515	1	2
Q4G0M1	Erythroferrone	ERFE C1QTNF15 CTRP15 FAM132B	5	2
Q92736	Ryanodine receptor 2	RYR2	4	2
Q8N3R9	Protein PALS1	PALS1 MPP5	2	2
P07355	Annexin A2	ANXA2 ANX2 ANX2L4 CAL1H LPC2D	2	2
Q9NPG1	Frizzled-3	FZD3	4	2
P43243	Matrin-3	MATR3 KIAA0723	11	2
Q8WWQ0	PH-interacting protein	PHIP DCAF14 WDR11	4	2
Q9NQS7	Inner centromere protein	INCENP	4	2
A4UGR9	Xin actin-binding repeat-containing protein 2	XIRP2 CMYA3	3	2
O94766	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3	B3GAT3	3	2	Hailey-Hailey disease Laron syndrome Larsen-like syndrome B3GAT3 type Marfan syndrome Rothmund-Thomson syndrome achondroplasia amblyopia aortic valve disease 1 aortic valve disease 2 aortic valve stenosis atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa 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 bicuspid aortic valve disease buphthalmos cancer cleft palate cleidocranial dysplasia clubfoot communicating hydrocephalus congenital heart disease craniosynostosis cutis laxa esotropia geroderma osteodysplasticum glaucoma hepatocellular carcinoma humeroradial synostosis hydrocephalus hydrophthalmos hyperopia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis isolated cleft palate juvenile glaucoma liver cancer liver carcinoma mal de Meleda mitral valve insufficiency mitral valve prolapse monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia obstructive hydrocephalus osteochondrodysplasia osteoporosis patent foramen ovale postinflammatory pulmonary fibrosis postural orthostatic tachycardia syndrome pulmonary fibrosis radioulnar synostosis refractive error restrictive dermopathy scoliosis senile degeneration of brain situs inversus strabismic amblyopia thoracic aortic aneurysm tuberous sclerosis
Q9C0K1	Metal cation symporter ZIP8	SLC39A8 BIGM103 ZIP8	2	2	Crohn's colitis Crohn's disease Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Laron syndrome Leigh disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Wilson disease achondroplasia acute chest syndrome alcohol dependence alcohol use disorder alternating hemiplegia of childhood androgen insensitivity syndrome anemia arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy astigmatism atherosclerosis atrial fibrillation attention deficit hyperactivity disorder autonomic neuropathy bacterial sepsis breast cancer breast carcinoma cancer central nervous system disease cerebral infarction cerebrovascular disease childhood leukemia colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ii congenital disorder of glycosylation In congenital disorder of glycosylation type I congenital disorder of glycosylation type IIn congenital disorder of glycosylation congenital nystagmus congestive heart failure coronary artery disease craniosynostosis dermatitis diabetes mellitus diabetic ketoacidosis dissociated nystagmus dystonia epilepsy essential hypertension focal hand dystonia generalized dystonia hemochromatosis hydrocephalus hyperopia hypertension hypertropia idiopathic scoliosis inflammatory bowel disease 1 inflammatory bowel disease intellectual disability iron metabolism disease kwashiorkor large intestine cancer learning disability left ventricular noncompaction leukemia macrocytic anemia marasmus mechanical strabismus mitochondrial metabolism disease mitochondrial myopathy nervous system disease neuroblastoma nicotine dependence nutrition disease obsolete infantile epileptic encephalopathy ophthalmoplegia osteoarthritis pathologic nystagmus protein-energy malnutrition pulmonary tuberculosis schizophrenia sensorineural hearing loss spontaneous ocular nystagmus strabismus systemic lupus erythematosus tuberculosis tuberculous pneumothorax type 2 diabetes mellitus ulcerative colitis visual epilepsy
Q13033	Striatin-3	STRN3 GS2NA SG2NA	1	2
Q02446	Transcription factor Sp4	SP4	22	2
Q9HAZ2	Histone-lysine N-methyltransferase PRDM16	PRDM16 KIAA1675 MEL1 PFM13	1	2
Q9NZJ0	Denticleless protein homolog	DTL CDT2 CDW1 DCAF2 L2DTL RAMP	2	2
Q8WTR4	Glycerophosphodiester phosphodiesterase domain-containing protein 5	GDPD5 GDE2	5	2	acute myeloid leukemia breast cancer breast carcinoma cancer colorectal cancer colorectal carcinoma embryoma large intestine cancer neuroblastoma neurodegenerative disease rheumatoid arthritis
O95996	Adenomatous polyposis coli protein 2	APC2 APCL	2	2
Q96B49	Mitochondrial import receptor subunit TOM6 homolog	TOMM6 OBTP TOM6	4	2
Q9NUQ8	ATP-binding cassette sub-family F member 3	ABCF3	1	2

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