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 **125251 - 125275** 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
P98172	Ephrin-B1	EFNB1 EFL3 EPLG2 LERK2	Homo sapiens (human)	13	9
Q08174	Protocadherin-1	PCDH1	Homo sapiens (human)	7	9
Q9Y2H9	Microtubule-associated serine/threonine-protein kinase 1	MAST1 KIAA0973 SAST	Homo sapiens (human)	2	9
O15393	Transmembrane protease serine 2	TMPRSS2 PRSS10	Homo sapiens (human)	2	9
D4A9Q5	Carboxypeptidase M	Cpm	Rattus norvegicus (Norway rat)	2	9
P20236	Gamma-aminobutyric acid receptor subunit alpha-3	Gabra3 Gabra-3	Rattus norvegicus (Norway rat)	4	9
P60755	MAM domain-containing glycosylphosphatidylinositol anchor protein 2	Mdga2 Mamdc1	Mus musculus (house mouse)	8	9
Q8BNA6	Protocadherin Fat 3	Fat3 Gm1132 Gm510	Mus musculus (house mouse)	26	9
Q6PK18	2-oxoglutarate and iron-dependent oxygenase domain-containing protein 3	OGFOD3 C17orf101	Homo sapiens (human)	2	9
Q8TB96	T-cell immunomodulatory protein	ITFG1 LNKN-1 TIP	Homo sapiens (human)	13	9
Q9BU23	Lipase maturation factor 2	LMF2 TMEM112B TMEM153	Homo sapiens (human)	3	9
Q6AXF6	SID1 transmembrane family member 1	Sidt1	Mus musculus (house mouse)	7	9
Q14571	Inositol 1,4,5-trisphosphate receptor type 2	ITPR2	Homo sapiens (human)	4	9
P48551	Interferon alpha/beta receptor 2	IFNAR2 IFNABR IFNARB	Homo sapiens (human)	6	9
Q9H5K3	Protein O-mannose kinase	POMK SGK196	Homo sapiens (human)	5	9	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bilateral optic nerve hypoplasia blindness cardiomyopathy cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A12 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism developmental coordination disorder distal myopathy endomyocardial fibrosis epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma hydranencephaly hydrocephalus hypertrophic cardiomyopathy hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lissencephaly lung small cell carcinoma mechanical strabismus megalocornea microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopia obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal degeneration retinal detachment rippling muscle disease 2 scoliosis senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly strabismus syndromic X-linked intellectual disability Najm type visual epilepsy
O43405	Cochlin	COCH COCH5B2	Homo sapiens (human)	8	9
D3ZQP6	Semaphorin 7A (John Milton Hagen blood group)	Sema7a	Rattus norvegicus (Norway rat)	1	9
P98086	Complement C1q subcomponent subunit A	C1qa	Mus musculus (house mouse)	4	9
P02656	Apolipoprotein C-III	APOC3	Homo sapiens (human)	3	9
P20827	Ephrin-A1	EFNA1 EPLG1 LERK1 TNFAIP4	Homo sapiens (human)	4	9	acute myocardial infarction adenocarcinoma adenoma allergic asthma arteriovenous malformation asthma benign giant cell tumor bladder carcinoma bone osteosarcoma botryoid rhabdomyosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system cancer childhood osteosarcoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon carcinoma colorectal cancer colorectal carcinoma coronary thrombosis cribriform carcinoma diabetic ketoacidosis distal arthrogryposis embryoma embryonal rhabdomyosarcoma esophagus squamous cell carcinoma gliosarcoma granular cell carcinoma hepatocellular carcinoma high grade glioma intestinal benign neoplasm intestinal cancer intrinsic asthma large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma malignant pleural mesothelioma melanoma mixed glioma myocardial infarction nonpapillary renal cell carcinoma obsolete type 1 diabetes mellitus 9 osteosarcoma ovarian cancer ovarian carcinoma papillary renal cell carcinoma pre-eclampsia primary pulmonary hypertension renal carcinoma renal cell carcinoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma silent myocardial infarction skin melanoma squamous cell carcinoma stomach cancer stomach carcinoma tongue squamous cell carcinoma transitional cell carcinoma tubular adenocarcinoma 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 urinary bladder cancer
Q99M71	Mammalian ependymin-related protein 1	Epdr1 Epdr2 Merp1 Merp2	Mus musculus (house mouse)	2	9
F6V328	Gamma-glutamyltransferase 1 (Fragment)	Ggt1	Mus musculus (house mouse)	1	9
Q6X4U4	Sclerostin domain-containing protein 1	SOSTDC1 USAG1	Homo sapiens (human)	2	9
E9PXF0	Protocadherin 17	Pcdh17	Mus musculus (house mouse)	6	9
G5E8K5	Ankyrin-3	Ank3	Mus musculus (house mouse)	10	9

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