GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
A0A141AZC1	MHC class I antigen (Fragment)	HLA-C	1	0
Q9NS73	MAP3K12-binding inhibitory protein 1	MBIP	1	1
R4S834	MHC class I antigen (Fragment)	HLA-C	1	0
A0A1C8DVV0	MHC class I antigen (Fragment)	HLA-B	1	0
A0A075B6T7	T cell receptor alpha variable 6	TRAV6 TCRAV5S1	1	0
A0A2H4G2B2	MHC class I antigen (Fragment)	HLA-B	1	0
A0A0G2JJ82	C3/C5 convertase (Fragment)	C2	1	0
A0A3G2YUZ9	MHC class I protein (Fragment)	HLA-C	1	0
I6SJ99	MHC class I antigen (Fragment)	HLA-C	1	0
A0A0P1IVW8	MHC Class I antigen (Fragment)	HLA-C	1	0
Q12986	Transcriptional repressor NF-X1	NFX1 NFX2	1	2
A0A0M3LB90	MHC class I antigen (Fragment)	HLA-B	1	0
H7C1Z0	Cysteine rich transmembrane BMP regulator 1 (Fragment)	CRIM1	1	0
P0CG37	Cryptic protein	CFC1	1	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 B-cell lymphoma Langerhans-cell histiocytosis Marfan syndrome Pick's disease Reye syndrome aromatase excess syndrome arteriosclerotic cardiovascular disease atherosclerosis atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect atrioventricular septal defect autoimmune hepatitis biliary atresia cancer cardiofaciocutaneous syndrome 1 cardiofaciocutaneous syndrome cardiovascular system disease cerebral degeneration congenital adrenal hyperplasia congenital heart disease coronary artery disease dextro-looped transposition of the great arteries disease of metabolism double outlet right ventricle embryoma essential thrombocythemia gallbladder disease gastric adenocarcinoma gastrointestinal system cancer heart disease hepatitis liver disease lymphoma malaria multiple types of congenital heart defects 6 myelodysplastic syndrome neuroblastoma non-Hodgkin lymphoma obsolete dextro-looped transposition of the great arteries 1 obsolete ymphosarcoma patent foramen ovale reticulosarcoma right atrial isomerism schizophrenia situs inversus tuberculosis tuberous sclerosis visceral heterotaxy
Q92562	Polyphosphoinositide phosphatase	FIG4 KIAA0274 SAC3	1	1	Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Joubert syndrome Laron syndrome Marfan syndrome Miller-Dieker lissencephaly syndrome Papillon-Lefevre disease Yunis-Varon syndrome achondroplasia agenesis of the corpus callosum with peripheral neuropathy amyotrophic lateral sclerosis type 11 amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease anxiety disorder atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal recessive distal hereditary motor neuronopathy 1 breast cancer breast carcinoma cardiomyopathy cataract communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cortical dysplasia-focal epilepsy syndrome cryptorchidism demyelinating disease demyelinating polyneuropathy depressive disorder distal arthrogryposis dysthymic disorder endomyocardial fibrosis enophthalmos epilepsy essential hypertension generalized anxiety disorder gingival recession gliosarcoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 2 hereditary spastic paraplegia 7 high grade glioma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hypertension hypertrophic cardiomyopathy hypospadias laryngostenosis lateral sclerosis lissencephaly lysosomal storage disease major depressive disorder melancholic depression microcephaly mixed glioma motor neuron disease motor peripheral neuropathy neuroblastoma neurodegenerative disease neuropathy neurotic disorder obsolete exophthalmos obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obstructive hydrocephalus orbital disease patent foramen ovale peripheral nervous system disease placental insufficiency polyhydramnios polyneuropathy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 primary pulmonary hypertension progressive muscular atrophy pyloric stenosis renal artery obstruction renovascular hypertension sclerocornea senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus status epilepticus subacute delirium syndactyly syndromic X-linked intellectual disability Najm type tetralogy of Fallot tuberous sclerosis ventricular septal defect
G1EQF2	MHC class I antigen (Fragment)	HLA-C	1	0
Q8TC92	Ecto-NOX disulfide-thiol exchanger 1	ENOX1	1	1
W8DXU8	TGF-beta receptor type-2	TGFBR2	1	0
Q14940	Sodium/hydrogen exchanger 5	SLC9A5 NHE5	1	0
A0A6S7XSP1	MHC class I antigen	HLA-B	1	0
A0A1S5QR43	MHC class I antigen (Fragment)	HLA-C	1	0
J7JHR0	MHC class I antigen (Fragment)	HLA-C	1	0
Q8NFX7	Syntaxin-binding protein 6	STXBP6	1	1
Q8TEQ0	Sorting nexin-29	SNX29 RUNDC2A	1	1
P01705	Immunoglobulin lambda variable 2-23	IGLV2-23	1	1

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