GlyCosmos Portal

Displaying entries **1 - 25** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
A6NFQ7	Divergent paired-related homeobox	DPRX	0	1
Q9UI30	Multifunctional methyltransferase subunit TRM112-like protein	TRMT112	0	1
A0A383S2I9	MHC class I antigen	HLA-C	1	0
Q13574	Diacylglycerol kinase zeta	DGKZ DAGK6	0	1	Clouston syndrome acute myocardial infarction adenocarcinoma adenoma adult lymphoma aplastic anemia bone osteosarcoma cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary thrombosis cribriform carcinoma diabetes mellitus embryoma giant cell glioblastoma glioblastoma granular cell carcinoma high grade glioma large intestine cancer myocardial infarction osteosarcoma pancytopenia prostate cancer prostate carcinoma pure red-cell aplasia schizophrenia silent myocardial infarction tubular adenocarcinoma type 2 diabetes mellitus
Q96RL7	Intermembrane lipid transfer protein VPS13A	VPS13A CHAC KIAA0986	2	14
Q9UP95	Solute carrier family 12 member 4	SLC12A4 KCC1	5	7
Q9ULC5	Long-chain-fatty-acid--CoA ligase 5	ACSL5 ACS5 FACL5	2	2	acute chest syndrome acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma anaplastic astrocytoma basal cell carcinoma breast cancer breast carcinoma cancer carcinoma celiac disease central nervous system cancer childhood cerebral astrocytoma colorectal cancer colorectal carcinoma congestive heart failure coronary thrombosis cribriform carcinoma embryoma endometrial carcinoma essential thrombocythemia familial hyperlipidemia fibrillary astrocytoma gemistocytic astrocytoma giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma hematologic cancer high grade glioma juvenile pilocytic astrocytoma large intestine cancer lung benign neoplasm lung carcinoma malignant astrocytoma migraine mixed glioma myelodysplastic syndrome myocardial infarction obesity pilocytic astrocytoma protoplasmic astrocytoma sarcomatoid carcinoma sebaceous carcinoma silent myocardial infarction steatotic liver disease subependymal giant cell astrocytoma sweat gland cancer systemic lupus erythematosus tubular adenocarcinoma
M9P934	MHC class I antigen (Fragment)	HLA-C	1	0
Q15642	Cdc42-interacting protein 4	TRIP10 CIP4 STOT STP	0	1
Q9BUJ0	Protein ABHD14A	ABHD14A	2	0
Q54A51	Basigin	hEMMPRIN BSG	3	0
Q5THR3	EF-hand calcium-binding domain-containing protein 6	EFCAB6 DJBP KIAA1672	1	1
Q1HP67	Lipoprotein, Lp(A)	LPA	3	0
Q7Z2Q7	Leucine-rich repeat-containing protein 70	LRRC70	5	1
Q9UHR5	SAP30-binding protein	SAP30BP HCNGP HTRG HTRP	25	3
Q13268	Dehydrogenase/reductase SDR family member 2, mitochondrial	DHRS2 SDR25C1	0	1
H0Y5E4	CD44 antigen (Fragment)	CD44	1	0
Q9NRW1	Ras-related protein Rab-6B	RAB6B	0	1
Q8N196	Homeobox protein SIX5	SIX5 DMAHP	0	1
A0A1C8DSH7	MHC class I antigen (Fragment)	HLA-B	1	0
M9PA20	MHC class I antigen (Fragment)	HLA-B	1	0
P08603	Complement factor H	CFH HF HF1 HF2	10	140
O43808	Peroxisomal membrane protein PMP34	SLC25A17 PMP34	0	1
Q8NCR0	UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 2	B3GALNT2	2	0	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 breast cancer breast carcinoma cancer cataract cerebral degeneration choreatic disease coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A11 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism depressive disorder developmental coordination disorder distal myopathy dysthymic disorder dystonia embryoma epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis focal epilepsy fundus dystrophy glaucoma hepatocellular carcinoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia lissencephaly liver cancer major depressive disorder mechanical strabismus melancholic depression meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia neurotic 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 obsolete infantile epileptic encephalopathy obsolete melancholia obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy partial motor epilepsy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly speech disorder stereotypic movement disorder strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type syndromic X-linked intellectual disability type 10 visual epilepsy
Q9BV94	ER degradation-enhancing alpha-mannosidase-like protein 2	EDEM2 C20orf31 C20orf49	4	0	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 Pick's disease Reye syndrome cerebral degeneration leiomyoma myofibroma schizophrenia uterine fibroid

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