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 **7076 - 7100** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q8N999	RNA ligase 1	RLIG1 C12orf29	Homo sapiens (human)	0	1
F1LTN6	Ig-like domain-containing protein	AABR07060872.1	Rattus norvegicus (Norway rat)	0	1
Q9Y2D9	Zinc finger protein 652	ZNF652 KIAA0924	Homo sapiens (human)	3	1
Q00325	Solute carrier family 25 member 3	SLC25A3 PHC	Homo sapiens (human)	0	1
B9PX11	Phospholipase/carboxylesterase	BN1205_058030	Toxoplasma gondii VEG	0	1
Q8BZ25	Ankyrin repeat and protein kinase domain-containing protein 1	Ankk1	Mus musculus (house mouse)	3	1
P49757	Protein numb homolog	NUMB C14orf41	Homo sapiens (human)	0	1
O89086	RNA-binding protein 3	Rbm3	Mus musculus (house mouse)	0	1
F4HPG4	Uncharacterized protein	At1g33050	Arabidopsis thaliana (thale cress)	0	1
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
Q86Y22	Collagen alpha-1(XXIII) chain	COL23A1	Homo sapiens (human)	0	1
M8A2S8	IQ domain-containing protein IQM3	TRIUR3_31639	Triticum urartu	0	1
Q00PI9	Heterogeneous nuclear ribonucleoprotein U-like protein 2	Hnrnpul2 Hnrpul2 Manp	Mus musculus (house mouse)	0	1
V5DHN7	RNA guanylyltransferase	TCDM_04464	Trypanosoma cruzi Dm28c	0	1
Q9VTH0	Procollagen-lysine,2-oxoglutarate 5-dioxygenase	Plod	Drosophila melanogaster (fruit fly)	5	1
Q6P9Z1	SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3	Smarcd3 Baf60c	Mus musculus (house mouse)	0	1
Q10567	AP-1 complex subunit beta-1	AP1B1 ADTB1 BAM22 CLAPB2	Homo sapiens (human)	0	1
V5B9G3	Isocitrate dehydrogenase [NADP]	TCDM_07659	Trypanosoma cruzi Dm28c	0	1
Q658T7	Putative protein FAM90A2P	FAM90A2P	Homo sapiens (human)	0	1
Q6XUX3	Dual serine/threonine and tyrosine protein kinase	DSTYK KIAA0472 RIP5 RIPK5 SGK496	Homo sapiens (human)	1	1
O35386	Phytanoyl-CoA dioxygenase, peroxisomal	Phyh Ln1 Lnap1 Pahx	Mus musculus (house mouse)	0	1
A0A6I8MX27	L-lactate dehydrogenase	Ldhb	Mus musculus (house mouse)	0	1
E9QP49	EH domain binding protein 1-like 1	Ehbp1l1	Mus musculus (house mouse)	0	1
Q9NSI2	Ribosome biogenesis protein SLX9 homolog	SLX9 C21orf70 FAM207A	Homo sapiens (human)	1	1
P28834	Isocitrate dehydrogenase [NAD] subunit 1, mitochondrial	IDH1	Saccharomyces cerevisiae S288C	6	1

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