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

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
A0A161I202	Lactotransferrin	LTF	Homo sapiens (human)	1	0
A0A5F9ZHR1	Biotinidase	BTD	Homo sapiens (human)	1	0
Q96MW5	Conserved oligomeric Golgi complex subunit 8	COG8	Homo sapiens (human)	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	Homo sapiens (human)	1	1
A0A2H4FZI9	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q8NG81	Olfactory receptor 2M7	OR2M7	Homo sapiens (human)	1	0
Q8WTU2	Scavenger receptor cysteine-rich domain-containing group B protein	SSC4D SRCRB4D	Homo sapiens (human)	1	1
E9PDI6	Voltage-dependent L-type calcium channel subunit alpha	CACNA1C	Homo sapiens (human)	1	0
P08559	Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial	PDHA1 PHE1A	Homo sapiens (human)	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	Homo sapiens (human)	1	0
M9P9F2	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
A0A7I2V3V9	Cathepsin F	CTSF	Homo sapiens (human)	1	0
Q96B01	RAD51-associated protein 1	RAD51AP1 PIR51	Homo sapiens (human)	1	2
O60895	Receptor activity-modifying protein 2	RAMP2	Homo sapiens (human)	1	0
A0A1D3KYN0	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
A0A186VNA7	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q12837	POU domain, class 4, transcription factor 2	POU4F2 BRN3B	Homo sapiens (human)	1	2
A0A1S5QQZ7	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q96GF5	PXDN protein (Fragment)	PXDN	Homo sapiens (human)	1	0
Q9NXX6	Non-structural maintenance of chromosomes element 4 homolog A	NSMCE4A C10orf86	Homo sapiens (human)	1	1
O00233	26S proteasome non-ATPase regulatory subunit 9	PSMD9	Homo sapiens (human)	1	2
A0A7I2V2Z5	NODAL modulator 3	NOMO3	Homo sapiens (human)	1	0
J7JWN0	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
F6IQG6	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q96MI9	Cytosolic carboxypeptidase 4	AGBL1 CCP4	Homo sapiens (human)	1	1

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