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 **17326 - 17350** of **18496** in total

« First

‹ Prev

…

690

691

692

693

694

695

696

697

698

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism ▼	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
A0A1S5QQY4	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
O95470	Sphingosine-1-phosphate lyase 1	SGPL1 KIAA1252	Homo sapiens (human)	1	2	Addison's disease Alzheimer's disease Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IMAGe syndrome Marfan syndrome Niemann-Pick disease Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome adrenal cortical hypofunction alveolar rhabdomyosarcoma anaplastic astrocytoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome autosomal recessive congenital ichthyosis 1 breast cancer breast carcinoma cancer childhood cerebral astrocytoma chondrodysplasia-pseudohermaphroditism syndrome chronic obstructive pulmonary disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital hypothyroidism congenital ptosis congestive heart failure coronary artery disease cryptorchidism embryoma endometrial cancer endometrial carcinoma epilepsy familial nephrotic syndrome fibrillary astrocytoma focal segmental glomerulosclerosis gastroenteritis gemistocytic astrocytoma glucose intolerance high grade glioma hyperglycemia hypertropia hypoglycemia hypogonadism hypothyroidism ichthyosis idiopathic interstitial pneumonia ileitis ileocolitis inherited metabolic disorder juvenile pilocytic astrocytoma keratosis follicularis kidney disease large intestine cancer laryngeal disease lipoid nephrosis lymphopenia malignant astrocytoma mechanical strabismus microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly mongolian spot multiple sclerosis myxedema nephrosis nephrotic syndrome type 14 nephrotic syndrome type 1 nephrotic syndrome neurodegenerative disease neuropathy obsolete congenital ichthyosiform erythroderma ophthalmoplegia peripheral nervous system disease pilocytic astrocytoma pneumonia polyneuropathy postinflammatory pulmonary fibrosis prediabetes syndrome proteinuria protoplasmic astrocytoma pseudoxanthoma elasticum ptosis pulmonary fibrosis sensorineural hearing loss situs inversus sphingolipidosis strabismus subependymal giant cell astrocytoma tracheal disease triple-A syndrome tuberous sclerosis uterine corpus cancer visual epilepsy
Q9Y6A4	Cilia- and flagella-associated protein 20	CFAP20 BUG22 C16orf80 GTL3	Homo sapiens (human)	0	1
O00712	Nuclear factor 1 B-type	NFIB	Homo sapiens (human)	6	1
Q9BY27	Protein DGCR6L	DGCR6L	Homo sapiens (human)	0	1
F4YTD5	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q8NBJ7	Inactive C-alpha-formylglycine-generating enzyme 2	SUMF2	Homo sapiens (human)	6	21
A0A5A4LHY7	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
Q70EK9	Ubiquitin carboxyl-terminal hydrolase 51	USP51	Homo sapiens (human)	0	1
D2DKK3	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q8WW96	CFHR3 protein	CFHR3	Homo sapiens (human)	1	0
Q7Z408	CUB and sushi domain-containing protein 2	CSMD2 KIAA1884	Homo sapiens (human)	35	0
P29218	Inositol monophosphatase 1	IMPA1 IMPA	Homo sapiens (human)	0	1	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 Duchenne muscular dystrophy Lewy body dementia Pick's disease Reye syndrome alcohol dependence alcohol use disorder antisocial personality disorder aplastic anemia 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 avoidant personality disorder bipolar disorder brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease central nervous system cancer cerebral artery occlusion cerebral atherosclerosis cerebral degeneration cerebral infarction cerebrovascular disease chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cone-rod dystrophy congenital muscular dystrophy conjunctivitis cryptosporidiosis cystitis delusional disorder dermatophytosis diabetes mellitus distal myopathy embryoma epilepsy essential hypertension facioscapulohumeral muscular dystrophy focal epilepsy fundus albipunctatus fungal infectious disease gallbladder disease gliosarcoma glycogen storage disease IV glycogen storage disease VI glycogen storage disease VII heart disease high grade glioma hypertension intellectual disability intracranial arteriosclerosis large intestine cancer learning disability limb-girdle muscular dystrophy liver disease lung benign neoplasm lung cancer lung carcinoma mixed glioma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 narcissistic personality disorder 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 oculopharyngeal muscular dystrophy ovarian cancer ovarian carcinoma paranoid schizophrenia partial motor epilepsy primary pulmonary hypertension retinitis pigmentosa rippling muscle disease 2 sickle cell anemia syndromic X-linked intellectual disability 94 systemic primary carnitine deficiency disease trigonitis type 2 diabetes mellitus visual epilepsy
D7NPQ0	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
O94880	PHD finger protein 14	PHF14 KIAA0783	Homo sapiens (human)	1	1
Q7RTR2	NLR family CARD domain-containing protein 3	NLRC3 NOD3	Homo sapiens (human)	0	1
Q9UK76	Jupiter microtubule associated homolog 1	JPT1 ARM2 HN1	Homo sapiens (human)	4	4
E7DRJ7	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q5SZI1	Low-density lipoprotein receptor class A domain-containing protein 2	LDLRAD2	Homo sapiens (human)	1	0
Q9UMX5	Neudesin	NENF CIR2 SPUF	Homo sapiens (human)	7	1
E2DHB8	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
A0A3G3NG95	MHC class I antigen (Fragment)	HLA-Cw	Homo sapiens (human)	1	0
Q52LJ0	Protein FAM98B	FAM98B	Homo sapiens (human)	0	1
Q6IQ16	Speckle-type POZ protein-like	SPOPL	Homo sapiens (human)	1	1
Q8NH09	Olfactory receptor 8S1	OR8S1	Homo sapiens (human)	1	0

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements