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 **18326 - 18350** 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
Q9P2N4	A disintegrin and metalloproteinase with thrombospondin motifs 9	ADAMTS9 KIAA1312	Homo sapiens (human)	11	5
Q9UP79	A disintegrin and metalloproteinase with thrombospondin motifs 8	ADAMTS8 METH2	Homo sapiens (human)	6	1
Q9UKP4	A disintegrin and metalloproteinase with thrombospondin motifs 7	ADAMTS7	Homo sapiens (human)	21	4
Q9UKP5	A disintegrin and metalloproteinase with thrombospondin motifs 6	ADAMTS6	Homo sapiens (human)	6	0
Q9UNA0	A disintegrin and metalloproteinase with thrombospondin motifs 5	ADAMTS5 ADAMTS11 ADMP2	Homo sapiens (human)	14	4
O75173	A disintegrin and metalloproteinase with thrombospondin motifs 4	ADAMTS4 KIAA0688	Homo sapiens (human)	2	3
O15072	A disintegrin and metalloproteinase with thrombospondin motifs 3	ADAMTS3 KIAA0366	Homo sapiens (human)	17	5
P59510	A disintegrin and metalloproteinase with thrombospondin motifs 20	ADAMTS20	Homo sapiens (human)	16	3
O95450	A disintegrin and metalloproteinase with thrombospondin motifs 2	ADAMTS2 PCINP PCPNI	Homo sapiens (human)	11	9
Q8TE59	A disintegrin and metalloproteinase with thrombospondin motifs 19	ADAMTS19	Homo sapiens (human)	5	0
Q8TE60	A disintegrin and metalloproteinase with thrombospondin motifs 18	ADAMTS18 ADAMTS21	Homo sapiens (human)	7	1
Q8TE56	A disintegrin and metalloproteinase with thrombospondin motifs 17	ADAMTS17	Homo sapiens (human)	7	2
Q8TE57	A disintegrin and metalloproteinase with thrombospondin motifs 16	ADAMTS16 KIAA2029	Homo sapiens (human)	7	1
Q8TE58	A disintegrin and metalloproteinase with thrombospondin motifs 15	ADAMTS15	Homo sapiens (human)	4	2
Q8WXS8	A disintegrin and metalloproteinase with thrombospondin motifs 14	ADAMTS14	Homo sapiens (human)	7	1
Q76LX8	A disintegrin and metalloproteinase with thrombospondin motifs 13	ADAMTS13 C9orf8	Homo sapiens (human)	27	15
P58397	A disintegrin and metalloproteinase with thrombospondin motifs 12	ADAMTS12	Homo sapiens (human)	15	17
Q9H324	A disintegrin and metalloproteinase with thrombospondin motifs 10	ADAMTS10	Homo sapiens (human)	7	3
Q9UHI8	A disintegrin and metalloproteinase with thrombospondin motifs 1	ADAMTS1 KIAA1346 METH1	Homo sapiens (human)	10	3
Q7L2J0	7SK snRNA methylphosphate capping enzyme	MEPCE BCDIN3	Homo sapiens (human)	4	1
P08253	72 kDa type IV collagenase	MMP2 CLG4A	Homo sapiens (human)	3	2
Q969T7	7-methylguanosine phosphate-specific 5'-nucleotidase	NT5C3B NT5C3L	Homo sapiens (human)	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
Q96D46	60S ribosomal export protein NMD3	NMD3	Homo sapiens (human)	0	1
P10809	60 kDa heat shock protein, mitochondrial	HSPD1 HSP60	Homo sapiens (human)	5	6

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