GlyCosmos Portal

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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 **4976 - 5000** 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
Q16799	Reticulon-1	RTN1 NSP	Homo sapiens (human)	2	1
K7P5H5	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9BY21	G-protein coupled receptor 87	GPR87 GPR95	Homo sapiens (human)	4	1
Q9Y5G6	Protocadherin gamma-A7	PCDHGA7	Homo sapiens (human)	2	1
O75121	Microfibrillar-associated protein 3-like	MFAP3L KIAA0626	Homo sapiens (human)	5	1
Q6ZU67	BEN domain-containing protein 4	BEND4 CCDC4	Homo sapiens (human)	0	1
P10124	Serglycin	SRGN PRG PRG1	Homo sapiens (human)	8	0	MHC class II deficiency Sertoli cell-only syndrome Y-linked spermatogenic failure 1 acute myeloid leukemia acute promyelocytic leukemia adenosine deaminase deficiency adult respiratory distress syndrome arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer candidiasis carcinoma central nervous system cancer childhood type dermatomyositis cleft palate colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary aneurysm coronary artery disease coronary stenosis degenerative disc disease dental caries dentin caries dermatomyositis diabetes mellitus diabetic cataract diabetic retinopathy diarrhea dilated cardiomyopathy 1A dilated cardiomyopathy disease of mental health embryoma enterocele esophagus squamous cell carcinoma essential hypertension giant cell glioblastoma glioblastoma gliosarcoma glucose intolerance gynecomastia hepatitis B hepatocellular carcinoma high grade glioma hypertension infant gynecomastia isolated cleft palate large intestine cancer liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus erythematosus male infertility malignant pleural mesothelioma mixed glioma multiple myeloma nasopharynx carcinoma newborn respiratory distress syndrome nutmeg liver oligospermia oral candidiasis osteoarthritis prediabetes syndrome psychotic disorder sarcomatoid carcinoma severe combined immunodeficiency type 2 diabetes mellitus
Q13148	TAR DNA-binding protein 43	TARDBP TDP43	Homo sapiens (human)	3	1
A0A4D6NZ61	HLA class I histocompatibility antigen	HLA-B	Homo sapiens (human)	1	0
O95070	Protein YIF1A	YIF1A 54TM HYIF1P YIF1	Homo sapiens (human)	0	1
Q5T4S7	E3 ubiquitin-protein ligase UBR4	UBR4 KIAA0462 KIAA1307 RBAF600 ZUBR1	Homo sapiens (human)	8	4
Q7Z5P9	Mucin-19	MUC19	Homo sapiens (human)	14	1
A0A0A7C7J9	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q96R67	Olfactory receptor 4C12	OR4C12	Homo sapiens (human)	1	0
Q8NEZ3	WD repeat-containing protein 19	WDR19 IFT144 KIAA1638	Homo sapiens (human)	0	1
D7NQY4	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q86SP6	Probable G-protein coupled receptor 149	GPR149 PGR10	Homo sapiens (human)	3	0
Q8NH74	Olfactory receptor 10A6	OR10A6	Homo sapiens (human)	1	0
P07237	Protein disulfide-isomerase	P4HB ERBA2L PDI PDIA1 PO4DB	Homo sapiens (human)	8	2
P00519	Tyrosine-protein kinase ABL1	ABL1 ABL JTK7	Homo sapiens (human)	3	1
P29083	General transcription factor IIE subunit 1	GTF2E1 TF2E1	Homo sapiens (human)	0	1
Q8NGI3	Olfactory receptor 56B1	OR56B1 OR56B1P	Homo sapiens (human)	1	0
Q9Y5P6	Mannose-1-phosphate guanyltransferase beta	GMPPB	Homo sapiens (human)	0	1	Bell's palsy Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Lambert-Eaton myasthenic syndrome Walker-Warburg syndrome agnosia amblyopia 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 centronuclear myopathy cleft palate clubfoot coloboma communicating hydrocephalus cone-rod dystrophy congenital muscular dystrophy-dystroglycanopathy A14 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy congenital myasthenic syndrome congenital nystagmus congenital ptosis congenital structural myopathy cryptorchidism developmental coordination disorder dissociated nystagmus distal myopathy endomyocardial fibrosis epilepsy esotropia facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy familial periodic paralysis fundus albipunctatus glaucoma holoprosencephaly 1 holoprosencephaly hydrocephalus hypertrophic cardiomyopathy hypertropia idiopathic generalized epilepsy intellectual disability isolated cleft palate isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy mechanical strabismus megalocornea meningocele microcephaly microphthalmia monocular esotropia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy 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 oligohydramnios ophthalmoplegia optic atrophy pathologic nystagmus ptosis retinal detachment retinitis pigmentosa rippling muscle disease 2 scoliosis senile degeneration of brain sensorineural hearing loss speech disorder spontaneous ocular nystagmus strabismic amblyopia strabismus syndromic X-linked intellectual disability 94 visual epilepsy
Q8IVN8	Somatomedin-B and thrombospondin type-1 domain-containing protein	SBSPON C8orf84 RPESP	Homo sapiens (human)	1	45
Q95IE7	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0

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