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 **1126 - 1150** 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
O35604	NPC intracellular cholesterol transporter 1	Npc1	Mus musculus (house mouse)	18	11
Q9BZQ6	ER degradation-enhancing alpha-mannosidase-like protein 3	EDEM3 C1orf22	Homo sapiens (human)	8	11	hepatitis C prostate cancer prostate carcinoma
Q7Z5N4	Protein sidekick-1	SDK1	Homo sapiens (human)	19	11
P18572	Basigin	Bsg	Mus musculus (house mouse)	3	11
Q5JPE7	BOS complex subunit NOMO2	NOMO2	Homo sapiens (human)	7	11
Q6N022	Teneurin-4	TENM4 KIAA1302 ODZ4 TNM4	Homo sapiens (human)	14	11
P28825	Meprin A subunit alpha	Mep1a	Mus musculus (house mouse)	10	11
P52803	Ephrin-A5	EFNA5 EPLG7 LERK7	Homo sapiens (human)	3	11	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Ambras type hypertrichosis universalis congenita IGSF1 deficiency syndrome Norum disease Pick's disease Reye syndrome Tangier disease abdominal aortic aneurysm abetalipoproteinemia acquired immunodeficiency syndrome acute lymphoblastic leukemia acute myeloid leukemia adult medulloblastoma amyotrophic lateral sclerosis anencephaly arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness breast cancer breast carcinoma bulimia nervosa cancer cardiovascular system disease cataract cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease childhood medulloblastoma chondrosarcoma choreaacanthocytosis colitis conduct disorder congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 coronary artery disease cystic fibrosis diffuse large B-cell lymphoma embryoma enophthalmos familial hypobetalipoproteinemia 1 gastric ulcer gastroenteritis heart disease hemiplegia hepatocellular carcinoma human immunodeficiency virus infectious disease hypobetalipoproteinemia hypolipoproteinemia hypothyroidism ileitis ileocolitis infertility inflammatory bowel disease 1 inflammatory bowel disease liver cancer lymphoblastic lymphoma medulloblastoma medullomyoblastoma melanotic medulloblastoma myxedema nicotine dependence nutmeg liver obsessive-compulsive disorder obsolete exophthalmos orbital disease peripheral vascular disease progressive muscular atrophy prostate cancer prostate carcinoma schizophrenia sclerocornea senile cataract spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy synovitis systemic lupus erythematosus tenosynovitis thrombocytopenia ulcerative colitis
Q6NUS6	Tectonic-3	TCTN3 C10orf61 TECT3	Homo sapiens (human)	6	11
P01344	Insulin-like growth factor II	IGF2	Homo sapiens (human)	8	11
P01048	T-kininogen 1	Map1	Rattus norvegicus (Norway rat)	4	11
P01872	Immunoglobulin heavy constant mu	Ighm Igh-6	Mus musculus (house mouse)	7	11
O95477	Phospholipid-transporting ATPase ABCA1	ABCA1 ABC1 CERP	Homo sapiens (human)	22	11
P01563	Interferon alpha-2	IFNA2 IFNA2A IFNA2B IFNA2C	Homo sapiens (human)	1	11
P02768	Albumin	ALB	Homo sapiens (human)	35	11
Q99KW9	T-cell immunomodulatory protein	Itfg1 D8Wsu49e Lnkn-1 Tip	Mus musculus (house mouse)	10	11
P54290	Voltage-dependent calcium channel subunit alpha-2/delta-1	Cacna2d1 Cacnl2a Cchl2a	Rattus norvegicus (Norway rat)	9	11
Q61739	Integrin alpha-6	Itga6	Mus musculus (house mouse)	8	11
Q9NT68	Teneurin-2	TENM2 KIAA1127 ODZ2 TNM2	Homo sapiens (human)	16	11
Q9ERC8	Cell adhesion molecule DSCAM	Dscam	Mus musculus (house mouse)	17	11
Q9UBS4	DnaJ homolog subfamily B member 11	DNAJB11 EDJ ERJ3 HDJ9	Homo sapiens (human)	3	11
Q9Y2G5	GDP-fucose protein O-fucosyltransferase 2	POFUT2 C21orf80 FUT13 KIAA0958	Homo sapiens (human)	3	11	Peters plus syndrome congenital disorder of glycosylation malaria popliteal pterygium syndrome schizophrenia
Q920P3	BMP/retinoic acid-inducible neural-specific protein 1	Brinp1 Brinp Dbc1 Dbccr1 Fam5a	Mus musculus (house mouse)	7	11
Q9Y6M7	Sodium bicarbonate cotransporter 3	SLC4A7 BT NBC2 NBC2B NBC3 NBCn1 SBC2 SLC4A6	Homo sapiens (human)	10	11
P02774	Vitamin D-binding protein	GC	Homo sapiens (human)	2	11

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