GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **1401 - 1425** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism ▲	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q6NUQ1	RAD50-interacting protein 1	RINT1	Homo sapiens (human)	2	1
Q95IA9	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q8N999	RNA ligase 1	RLIG1 C12orf29	Homo sapiens (human)	0	1
Q96RQ3	Methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial	MCCC1 MCCA	Homo sapiens (human)	2	2
Q9NS75	Cysteinyl leukotriene receptor 2	CYSLTR2 CYSLT2 CYSLT2R	Homo sapiens (human)	4	0
Q9Y2D9	Zinc finger protein 652	ZNF652 KIAA0924	Homo sapiens (human)	3	1
P08519	Apolipoprotein(a)	LPA	Homo sapiens (human)	24	31
Q00325	Solute carrier family 25 member 3	SLC25A3 PHC	Homo sapiens (human)	0	1
E0X9Q2	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
P16233	Pancreatic triacylglycerol lipase	PNLIP	Homo sapiens (human)	1	0	acute myeloid leukemia acute pancreatitis cancer central nervous system cancer diabetes mellitus gliosarcoma high grade glioma mixed glioma obesity obsolete steatorrhea pancreatic cancer pancreatic carcinoma pancreatitis thrombocytopenia tropical sprue type 2 diabetes mellitus
O75578	Integrin alpha-10	ITGA10	Homo sapiens (human)	11	0
Q15107	Pregnancy-specific beta-1 glycoprotein (Fragment)	PSG1	Homo sapiens (human)	3	0
A0A6V6XYD9	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
A0A2H1MYD0	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
P26010	Integrin beta-7	ITGB7	Homo sapiens (human)	8	7
P49757	Protein numb homolog	NUMB C14orf41	Homo sapiens (human)	0	1
Q9UQ13	Leucine-rich repeat protein SHOC-2	SHOC2 KIAA0862	Homo sapiens (human)	1	2
A0A3S6RG16	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
D6MLC2	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
D3U3W6	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9UBM7	7-dehydrocholesterol reductase	DHCR7 D7SR	Homo sapiens (human)	0	1	3-methylglutaconic aciduria Behcet's disease Dandy-Walker syndrome Hailey-Hailey disease Laron syndrome Marfan syndrome Meckel syndrome Potter's syndrome Rapp-Hodgkin syndrome Rothmund-Thomson syndrome Smith-Lemli-Opitz syndrome X-linked ichthyosis achondroplasia ankyloblepharon-ectodermal defects-cleft lip/palate syndrome arteriosclerotic cardiovascular disease atherosclerosis atrioventricular septal defect autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal dominant polycystic kidney disease 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 bilateral optic nerve hypoplasia bilateral renal aplasia cardiovascular system disease choanal atresia coloboma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital disorder of glycosylation type II congenital disorder of glycosylation type IIc coronary artery disease cutis laxa dermatitis diabetes mellitus diabetic ketoacidosis fissured tongue glaucoma glycoproteinosis heart disease hepatitis C hepatocellular carcinoma hydrocephalus hypohidrotic ectodermal dysplasia hypospadias immune system disease intellectual disability interstitial nephritis large intestine cancer learning disability leukocyte adhesion deficiency 2 leukocyte adhesion deficiency lingual-facial-buccal dyskinesia liver cancer liver cirrhosis mal de Meleda microcephaly movement disease multiple sclerosis nutmeg liver obsolete type 1 diabetes mellitus 9 oligohydramnios osteomalacia periventricular nodular heterotopia photosensitive epilepsy photosensitivity disease placental insufficiency polycystic ovary syndrome polydactyly polyhydramnios pyelitis pyelonephritis restrictive dermopathy rheumatoid arthritis rickets scoliosis sensorineural hearing loss situs inversus syndromic X-linked intellectual disability type 10 tongue disease tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ventricular septal defect
C9J5Z5	FAM3 metabolism regulating signaling molecule D (Fragment)	FAM3D	Homo sapiens (human)	1	0
Q86Y22	Collagen alpha-1(XXIII) chain	COL23A1	Homo sapiens (human)	0	1
U5ISX7	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
H6V088	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0

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