GlyCosmos Portal

Displaying entries **5976 - 6000** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q8NHW5	Putative ribosomal protein uL10-like	RPLP0P6	0	1
Q15436	Protein transport protein Sec23A	SEC23A	34	1
Q13418	Integrin-linked protein kinase	ILK ILK1 ILK2	0	1
B4DLN1	cDNA FLJ60124, highly similar to Mitochondrial dicarboxylate carrier	SLC25A10	0	1
O00481	Butyrophilin subfamily 3 member A1	BTN3A1 BTF5	3	1
P35080	Profilin-2	PFN2	0	1
O14617	AP-3 complex subunit delta-1	AP3D1	0	1
Q4G0U5	Cilia- and flagella-associated protein 221	CFAP221 PCDP1	0	1
Q16881	Thioredoxin reductase 1, cytoplasmic	TXNRD1 GRIM12 KDRF	0	1
Q9NZM5	Ribosome biogenesis protein NOP53	NOP53 GLT GLTSCR2 PICT1	0	1
Q8NGX6	Olfactory receptor 10R2	OR10R2	3	1
P50549	ETS translocation variant 1	ETV1 ER81	0	1
P08708	Small ribosomal subunit protein eS17	RPS17 RPS17L	0	1
Q12979	Active breakpoint cluster region-related protein	ABR	1	1
P36896	Activin receptor type-1B	ACVR1B ACVRLK4 ALK4	1	1
P35240	Merlin	NF2 SCH	0	1
P54840	Glycogen [starch] synthase, liver	GYS2	1	1	Baraitser-Winter syndrome Fraser syndrome Gerstmann-Straussler-Scheinker syndrome Goldenhar syndrome Gorham's disease Joubert syndrome 1 Joubert syndrome Laron syndrome Moebius syndrome Sakati-Nyhan syndrome Warburg micro syndrome 1 Warburg micro syndrome 2 Warburg micro syndrome 3 Warburg micro syndrome 4 Weissenbacher-Zweymuller syndrome achondroplasia adult medulloblastoma branchiootic syndrome cancer childhood medulloblastoma cystinuria disease of metabolism epilepsy familial hyperlipidemia galactosemia gestational diabetes glucosephosphate dehydrogenase deficiency glycogen storage disease III glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatitis B hepatocellular carcinoma hyperglycemia hypoglycemia liver cancer medulloblastoma medullomyoblastoma melanotic medulloblastoma orofaciodigital syndrome I orofaciodigital syndrome X orofaciodigital syndrome polycystic ovary syndrome visual epilepsy
Q9BYC5	Alpha-(1,6)-fucosyltransferase	FUT8	4	1	Laron syndrome achondroplasia adenocarcinoma adenoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis brain disease breast cancer breast carcinoma bronchus cancer bronchus carcinoma buphthalmos cancer chronic fatigue syndrome chronic myeloid leukemia chronic obstructive pulmonary disease colorectal cancer colorectal carcinoma congenital disorder of glycosylation coronary artery disease embryoma encephalitis encephalomyelitis epilepsy follicular adenoma glaucoma hepatitis A hepatitis C hepatitis hepatocellular carcinoma hydrophthalmos idiopathic interstitial pneumonia intellectual disability juvenile glaucoma large intestine cancer learning disability liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma melanoma microcephaly microcystic adenoma myelitis ovarian cancer ovarian carcinoma pancreatic ductal adenocarcinoma pancreatic intraductal papillary-mucinous neoplasm papillary adenoma papillary carcinoma placental insufficiency polyhydramnios postinflammatory pulmonary fibrosis prostate cancer prostate carcinoma pseudomyxoma peritonei pulmonary emphysema pulmonary fibrosis schizophrenia scoliosis skin melanoma visual epilepsy
P27658	Collagen alpha-1(VIII) chain	COL8A1 C3orf7	1	1
Q9GZV4	Eukaryotic translation initiation factor 5A-2	EIF5A2	0	1
O75952	Calcium-binding tyrosine phosphorylation-regulated protein	CABYR CBP86 FSP2	1	1
P62330	ADP-ribosylation factor 6	ARF6	0	1
Q9H609	Zinc finger protein 576	ZNF576	0	1
Q9Y3D7	Mitochondrial import inner membrane translocase subunit TIM16	PAM16 MAGMAS TIM16 TIMM16	0	1
Q96CF2	Charged multivesicular body protein 4c	CHMP4C SHAX3	0	1

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