GlyCosmos Portal

Displaying entries **15976 - 16000** of **18496** in total

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UniProt ID ▲	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9C0D2	Centrosomal protein of 295 kDa	CEP295 KIAA1731	8	4
Q9C0D3	Protein zyg-11 homolog B	ZYG11B KIAA1730	0	1
Q9C0D5	Protein TANC1	TANC1 KIAA1728	13	1
Q9C0D7	Probable ribonuclease ZC3H12C	ZC3H12C KIAA1726 MCPIP3	1	1
Q9C0E2	Exportin-4	XPO4 KIAA1721	2	3
Q9C0E4	Glutamate receptor-interacting protein 2	GRIP2 KIAA1719	2	1
Q9C0E8	Endoplasmic reticulum junction formation protein lunapark	LNPK KIAA1715 LNP	1	1
Q9C0F0	Putative Polycomb group protein ASXL3	ASXL3 KIAA1713	11	1
Q9C0F1	Centrosomal protein of 44 kDa	CEP44 KIAA1712	4	1
Q9C0G0	Zinc finger protein 407	ZNF407 KIAA1703	0	1
Q9C0H2	Protein tweety homolog 3	TTYH3 KIAA1691	3	8
Q9C0H9	SRC kinase signaling inhibitor 1	SRCIN1 KIAA1684 P140 SNIP	2	1
Q9C0I3	Serine-rich coiled-coil domain-containing protein 1	CCSER1 FAM190A KIAA1680	2	2
Q9C0I4	Thrombospondin type-1 domain-containing protein 7B	THSD7B KIAA1679	11	0
Q9C0I9	Leucine-rich repeat-containing protein 27	LRRC27 KIAA1674	0	1
Q9C0J1	N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 4	B3GNT4	1	0
Q9C0J8	pre-mRNA 3' end processing protein WDR33	WDR33 WDC146	2	1
Q9C0K0	B-cell lymphoma/leukemia 11B	BCL11B CTIP2 RIT1	0	1
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
Q9C0K3	Actin-related protein 3C	ACTR3C ARP11	1	1
Q9C0K7	STE20-related kinase adapter protein beta	STRADB ALS2CR2 ILPIP	2	1
Q9GIM9	MHC class I antigen (Fragment)	HLA-B	1	0
Q9GIP1	MHC class I antigen (Fragment)	HLA-C	1	0
Q9GJ19	MHC class I antigen (Fragment)	HLA-B	1	0
Q9GJ26	MHC class I chain-related A antigen (Fragment)	MICA	1	0

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