GlyCosmos Portal

Displaying entries **2826 - 2850** of **18496** in total

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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9BTC8	Metastasis-associated protein MTA3	MTA3 KIAA1266	0	1
Q9BTC0	Death-inducer obliterator 1	DIDO1 C20orf158 DATF1 KIAA0333	32	2
Q9BTA9	WW domain-containing adapter protein with coiled-coil	WAC KIAA1844	11	1
Q9BT81	Transcription factor SOX-7	SOX7	0	1
Q9BT78	COP9 signalosome complex subunit 4	COPS4 CSN4	1	2
Q9BT76	Uroplakin-3b	UPK3B	1	0
Q9BT73	Proteasome assembly chaperone 3	PSMG3 C7orf48 PAC3	0	1
Q9BT30	Alpha-ketoglutarate-dependent dioxygenase alkB homolog 7, mitochondrial	ALKBH7 ABH7 SPATA11	0	1
Q9BT25	HAUS augmin-like complex subunit 8	HAUS8 HICE1	0	1
Q9BT22	Chitobiosyldiphosphodolichol beta-mannosyltransferase	ALG1 HMAT1 HMT1	0	1	B-cell lymphoma Cauda equina syndrome Creutzfeldt-Jakob disease Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Walker-Warburg syndrome amyotrophic lateral sclerosis type 1 breast cancer breast carcinoma breast fibroadenoma bronchus cancer bronchus carcinoma cancer cardiomyopathy cerebral degeneration cerebral infarction cerebrovascular disease colon cancer colonic benign neoplasm congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A1 diabetes mellitus endomyocardial fibrosis enophthalmos epilepsy familial hypertrophic cardiomyopathy familial nephrotic syndrome focal epilepsy glomerulonephritis goiter hepatocellular carcinoma hyperthyroidism hypertrophic cardiomyopathy hypogonadism kidney disease laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus nephritis lymphoma malignant pleural mesothelioma microcephaly nephritis nephrosis nephrotic syndrome type 1 nephrotic syndrome neurogenic bladder nodular goiter obsolete exophthalmos obsolete ymphosarcoma orbital disease partial motor epilepsy placental insufficiency pyoureter reticulosarcoma schizophrenia scoliosis systemic lupus erythematosus thyroid gland disease thyrotoxicosis type 2 diabetes mellitus urinary tract obstruction visual epilepsy
Q9BT09	Protein canopy homolog 3	CNPY3 CTG4A ERDA5 PRAT4A TNRC5	6	14
Q9BT04	Protein fuzzy homolog	FUZ FY	1	1
Q9BSV6	tRNA-splicing endonuclease subunit Sen34	TSEN34 LENG5 SEN34	0	1
Q9BSQ5	Cerebral cavernous malformations 2 protein	CCM2 C7orf22	2	1
Q9BSN7	Transmembrane protein 204	TMEM204 C16orf30 CLP24	1	0
Q9BSL1	Ubiquitin-associated domain-containing protein 1	UBAC1 GBDR1 KPC2 UBADC1	1	2
Q9BSK2	Solute carrier family 25 member 33	SLC25A33	0	1
Q9BSJ8	Extended synaptotagmin-1	ESYT1 FAM62A KIAA0747 MBC2	2	2
Q9BSJ6	Protein PIMREG	PIMREG CATS FAM64A RCS1	0	1
Q9BSJ2	Gamma-tubulin complex component 2	TUBGCP2 GCP2	1	1
Q9BSH4	Translational activator of cytochrome c oxidase 1	TACO1 CCDC44	1	1
Q9BSG0	Protease-associated domain-containing protein 1	PRADC1 C2orf7 PAP21	1	0
Q9BSF8	BTB/POZ domain-containing protein 10	BTBD10 GMRP1	0	1
Q9BSD7	Cancer-related nucleoside-triphosphatase	NTPCR C1orf57	0	1
Q9BSA4	Protein tweety homolog 2	TTYH2 C17orf29	4	0

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