GlyCosmos Portal

Displaying entries **5726 - 5750** of **18496** in total

« First

‹ Prev

…

226

227

228

229

230

231

232

233

234

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
A0A161I202	Lactotransferrin	LTF	1	0
A0A5F9ZHR1	Biotinidase	BTD	1	0
Q96MW5	Conserved oligomeric Golgi complex subunit 8	COG8	1	1	Dandy-Walker syndrome Unverricht-Lundborg syndrome alternating esotropia alveolar soft part sarcoma blepharospasm brain disease clubfoot colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation type II congenital disorder of glycosylation type IIh congenital disorder of glycosylation developmental and epileptic encephalopathy 36 early myoclonic encephalopathy epilepsy esophageal cancer esophageal carcinoma focal hand dystonia hepatocellular carcinoma hydrocephalus hypoglycemia intellectual disability isolated elevated serum creatine phosphokinase levels large intestine cancer learning disability liver cancer lung benign neoplasm lung carcinoma microcephaly protein-losing enteropathy scoliosis status epilepticus stomach cancer stomach carcinoma visual epilepsy
P82909	Alpha-ketoglutarate dehydrogenase component 4	KGD4 MRPS36	1	1
A0A2H4FZI9	MHC class I antigen (Fragment)	HLA-C	1	0
Q8NG81	Olfactory receptor 2M7	OR2M7	1	0
Q8WTU2	Scavenger receptor cysteine-rich domain-containing group B protein	SSC4D SRCRB4D	1	1
E9PDI6	Voltage-dependent L-type calcium channel subunit alpha	CACNA1C	1	0
P08559	Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial	PDHA1 PHE1A	1	1	Coffin-Lowry syndrome Leigh disease Lewy body dementia Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease West syndrome abdominal obesity-metabolic syndrome 1 anemia arthritis arthropathy basal ganglia disease bile duct adenocarcinoma bile duct carcinoma blepharospasm cancer carcinoma cardiomyopathy cerebellar ataxia cerebellar disease cerebral degeneration cerebral palsy cholangiocarcinoma communicating hydrocephalus cone-rod dystrophy congenital nystagmus congenital ptosis coronary artery disease dissociated nystagmus dystonia embryoma endomyocardial fibrosis epilepsy episodic ataxia esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma familial hypertrophic cardiomyopathy fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome focal hand dystonia fundus albipunctatus generalized dystonia head and neck squamous cell carcinoma hemiplegia hepatocellular carcinoma hydrocephalus hypertrichosis hypertrophic cardiomyopathy hypertropia inherited metabolic disorder intellectual disability intrahepatic cholangiocarcinoma lactic acidosis learning disability leukodystrophy lingual-facial-buccal dyskinesia liver cancer macrocytic anemia mechanical strabismus microcephaly mitochondrial metabolism disease mitochondrial myopathy movement disease neuropathy obsolete infantile epileptic encephalopathy obstructive hydrocephalus ophthalmoplegia optic atrophy osteoarthritis pathologic nystagmus peripheral nervous system disease placental insufficiency prostate cancer prostate carcinoma ptosis pyruvate carboxylase deficiency disease pyruvate decarboxylase deficiency retinitis pigmentosa sarcomatoid carcinoma senile degeneration of brain sensorineural hearing loss spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy spontaneous ocular nystagmus stomach cancer stomach carcinoma strabismus syndromic X-linked intellectual disability 94 ventricular septal defect visual epilepsy
A0A186VN77	MHC class I antigen (Fragment)	HLA-C	1	0
M9P9F2	MHC class I antigen (Fragment)	HLA-C	1	0
A0A7I2V3V9	Cathepsin F	CTSF	1	0
Q96B01	RAD51-associated protein 1	RAD51AP1 PIR51	1	2
O60895	Receptor activity-modifying protein 2	RAMP2	1	0
A0A1D3KYN0	MHC class I antigen	HLA-C	1	0
A0A186VNA7	MHC class I antigen (Fragment)	HLA-C	1	0
Q12837	POU domain, class 4, transcription factor 2	POU4F2 BRN3B	1	2
A0A1S5QQZ7	MHC class I antigen (Fragment)	HLA-B	1	0
Q96GF5	PXDN protein (Fragment)	PXDN	1	0
Q9NXX6	Non-structural maintenance of chromosomes element 4 homolog A	NSMCE4A C10orf86	1	1
O00233	26S proteasome non-ATPase regulatory subunit 9	PSMD9	1	2
A0A7I2V2Z5	NODAL modulator 3	NOMO3	1	0
J7JWN0	MHC class I antigen (Fragment)	HLA-C	1	0
F6IQG6	MHC class I antigen (Fragment)	HLA-C	1	0
Q96MI9	Cytosolic carboxypeptidase 4	AGBL1 CCP4	1	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

Summary

International Collaboration

Acknowledgements