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 **109401 - 109425** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q8VYH3	YTH domain-containing family protein	ECT10 MCK7.6 MCK7_6	Arabidopsis thaliana (thale cress)	0	1
A0A1D5RMI8	ALMS1, centrosome and basal body associated	Alms1	Mus musculus (house mouse)	1	1
Q8N0Y7	Probable phosphoglycerate mutase 4	PGAM4 PGAM3	Homo sapiens (human)	0	1	male infertility
Q4DWX7	Mitochondrial import receptor subunit	Tc00.1047053510729.80	Trypanosoma cruzi strain CL Brener	0	1
Q9EQP2	EH domain-containing protein 4	Ehd4 Past2	Mus musculus (house mouse)	0	1
Q9NR64	Kelch-like protein 1	KLHL1 KIAA1490	Homo sapiens (human)	1	1
Q6PD31	Trafficking kinesin-binding protein 1	Trak1	Mus musculus (house mouse)	11	1
P62877	E3 ubiquitin-protein ligase RBX1	RBX1 RNF75 ROC1	Homo sapiens (human)	0	1
V5DJS7	Dihydroxyacetone phosphate acyltransferase	TCDM_03538	Trypanosoma cruzi Dm28c	0	1
Q4DMH3	Prefoldin subunit 3	Tc00.1047053508881.120	Trypanosoma cruzi strain CL Brener	0	1
V5BWE3	Aminopeptidase	TCDM_00653	Trypanosoma cruzi Dm28c	0	1
Q8VDU5	SNF-related serine/threonine-protein kinase	Snrk	Mus musculus (house mouse)	0	1
A0A384LIC3	Protein kinase domain-containing protein	At1g79570	Arabidopsis thaliana (thale cress)	0	1
V5AXL4	Uncharacterized protein	TCDM_06058	Trypanosoma cruzi Dm28c	0	1
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
Q8BX22	Sal-like protein 4	Sall4	Mus musculus (house mouse)	6	1
P82909	Alpha-ketoglutarate dehydrogenase component 4	KGD4 MRPS36	Homo sapiens (human)	1	1
P52569	Cationic amino acid transporter 2	SLC7A2 ATRC2 CAT2	Homo sapiens (human)	3	1
Q8WTU2	Scavenger receptor cysteine-rich domain-containing group B protein	SSC4D SRCRB4D	Homo sapiens (human)	1	1
V5B6F9	Uncharacterized protein	TCDM_02333	Trypanosoma cruzi Dm28c	0	1
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
Q8BZT9	Purine nucleoside phosphorylase LACC1	Lacc1 Famin	Mus musculus (house mouse)	0	1
Q13228	Methanethiol oxidase	SELENBP1 SBP	Homo sapiens (human)	0	1
Q71F23	Centromere protein U	CENPU ICEN24 KLIP1 MLF1IP PBIP1	Homo sapiens (human)	2	1
Q12772	Sterol regulatory element-binding protein 2	SREBF2 BHLHD2 SREBP2	Homo sapiens (human)	3	1

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