GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
A0A678ZXE4	MHC class I antigen	HLA-C	1	0
Q02218	2-oxoglutarate dehydrogenase complex component E1	OGDH	1	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 Creutzfeldt-Jakob disease Laron syndrome Leigh disease Pick's disease Reye syndrome achondroplasia alternating hemiplegia of childhood arteriosclerotic cardiovascular disease atherosclerosis autonomic neuropathy breast cancer cancer central nervous system disease cerebral degeneration colorectal cancer colorectal carcinoma communicating hydrocephalus congestive heart failure coronary artery disease embryoma hydrocephalus lactic acidosis large intestine cancer lingual-facial-buccal dyskinesia movement disease nervous system disease neuroblastoma neurodegenerative disease obstructive hydrocephalus phenylketonuria placental insufficiency primary biliary cholangitis pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency senile degeneration of brain status epilepticus urea cycle disorder viral infectious disease
Q6P1M3	LLGL scribble cell polarity complex component 2	LLGL2	1	1
G9I2K9	MHC Class I antigen (Fragment)	HLA-B	1	0
A0A1S5QQY4	MHC class I antigen (Fragment)	HLA-B	1	0
O95470	Sphingosine-1-phosphate lyase 1	SGPL1 KIAA1252	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
F4YTD5	MHC class I antigen (Fragment)	HLA-B	1	0
A0A5A4LHY7	MHC class I antigen	HLA-C	1	0
D2DKK3	MHC class I antigen (Fragment)	HLA-C	1	0
Q8WW96	CFHR3 protein	CFHR3	1	0
D7NPQ0	MHC class I antigen (Fragment)	HLA-B	1	0
O94880	PHD finger protein 14	PHF14 KIAA0783	1	1
E7DRJ7	MHC class I antigen (Fragment)	HLA-B	1	0
Q5SZI1	Low-density lipoprotein receptor class A domain-containing protein 2	LDLRAD2	1	0
E2DHB8	MHC class I antigen (Fragment)	HLA-C	1	0
A0A3G3NG95	MHC class I antigen (Fragment)	HLA-Cw	1	0
Q6IQ16	Speckle-type POZ protein-like	SPOPL	1	1
Q8NH09	Olfactory receptor 8S1	OR8S1	1	0
Q9NWK9	Box C/D snoRNA protein 1	ZNHIT6 BCD1 C1orf181	1	1
P36980	Complement factor H-related protein 2	CFHR2 CFHL2 FHR2 HFL3	1	5
A0A0C4DH30	Probable non-functional immunoglobulin heavy variable 3-16	IGHV3-16	1	0
P59827	BPI fold-containing family B member 4	BPIFB4 C20orf186 LPLUNC4	1	0
A0A6V6XZ39	MHC class I antigen	HLA-B	1	0
A0A1C3PHY4	MHC class I antigen	HLA-C	1	0
C9WCT0	MHC class I antigen (Fragment)	HLA-B	1	0

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