GlyCosmos Portal

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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P39900	Macrophage metalloelastase	HME MMP12	2	0	Barrett's esophagus abdominal aortic aneurysm arteriosclerosis coronary aneurysm coronary artery disease esophagus adenocarcinoma multiple sclerosis
P39880	Homeobox protein cut-like 1	CUTL1 CUX1	10	2
P39748	Flap endonuclease 1	FEN1 RAD2	1	1
P39086	Glutamate receptor ionotropic, kainate 1	GLUR5 GRIK1	9	0	childhood absence epilepsy
P39060	Collagen alpha-1(XVIII) chain	COL18A1	39	21	primary angle-closure glaucoma
P39059	Collagen alpha-1(XV) chain	COL15A1	28	9
P39023	Large ribosomal subunit protein uL3	OK/SW-cl.32 RPL3	1	1
P39019	Small ribosomal subunit protein eS19	RPS19	2	1	Diamond-Blackfan anemia 1 Diamond-Blackfan anemia
P38935	DNA-binding protein SMUBP-2	IGHMBP2 SMBP2 SMUBP2	2	0	Charcot-Marie-Tooth disease axonal type 2S autosomal recessive distal hereditary motor neuronopathy 1
P38919	Eukaryotic initiation factor 4A-III	DDX48 EIF4A3 KIAA0111	3	1	intellectual disability
P38646	Stress-70 protein, mitochondrial	GRP75 HSPA9 HSPA9B mt-HSP70	5	3	Parkinson's disease autosomal dominant sideroblastic anemia 4
P38606	V-type proton ATPase catalytic subunit A	ATP6A1 ATP6V1A ATP6V1A1 VPP2	5	1	autosomal recessive cutis laxa type IID developmental and epileptic encephalopathy 93
P38571	Lysosomal acid lipase/cholesteryl ester hydrolase	LIPA	9	46	Wolman disease cholesterol ester storage disease lysosomal acid lipase deficiency
P38570	Integrin alpha-E	ITGAE	11	2
P38567	Hyaluronidase PH-20	HYAL3 PH20 SPAM1	6	0
P38484	Interferon gamma receptor 2	IFNGR2 IFNGT1	7	3	immunodeficiency 28
P38435	Vitamin K-dependent gamma-carboxylase	GC GGCX	5	7	combined deficiency of vitamin K-dependent clotting factors 1
P38398	Breast cancer type 1 susceptibility protein	BRCA1 RNF53	2	3	Fanconi anemia complementation group S breast adenocarcinoma breast cancer cervical cancer cervix uteri carcinoma in situ colon cancer colorectal cancer esophagus squamous cell carcinoma hereditary breast ovarian cancer syndrome hypertension lung non-small cell carcinoma nasopharynx carcinoma ovarian cancer pancreatic cancer prostate cancer stomach cancer urinary bladder cancer
P38159	RNA-binding motif protein, X chromosome	HNRPG RBMX RBMXP1	4	2	X-linked mental retardation Gustavson type syndromic X-linked intellectual disability Shashi type
P38117	Electron transfer flavoprotein subunit beta	ETFB FP585	2	1	multiple acyl-CoA dehydrogenase deficiency
P37840	Alpha-synuclein	NACP PARK1 SNCA	6	2	Alzheimer's disease Lewy body dementia Parkinson's disease 1 Parkinson's disease 4 Parkinson's disease
P37802	Transgelin-2	CDABP0035 KIAA0120 TAGLN2	7	3
P37288	Vasopressin V1a receptor	AVPR1 AVPR1A	3	0	hypertension
P37287	Phosphatidylinositol N-acetylglucosaminyltransferase subunit A	PIGA	1	0	multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
P37275	Zinc finger E-box-binding homeobox 1	AREB6 TCF8 ZEB1	2	0	Fuchs' endothelial dystrophy posterior polymorphous corneal dystrophy 3

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