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 **5226 - 5250** 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
A0A5F9ZHR1	Biotinidase	BTD	Homo sapiens (human)	1	0
P01033	Metalloproteinase inhibitor 1	TIMP1 CLGI TIMP	Homo sapiens (human)	2	135
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
Q9BZ11	Disintegrin and metalloproteinase domain-containing protein 33	ADAM33 C20orf153	Homo sapiens (human)	5	0
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
P52569	Cationic amino acid transporter 2	SLC7A2 ATRC2 CAT2	Homo sapiens (human)	3	1
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
E9PDZ0	Complement C2	C2	Homo sapiens (human)	5	0
P13686	Tartrate-resistant acid phosphatase type 5	ACP5	Homo sapiens (human)	3	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
Q8N1G1	RNA exonuclease 1 homolog	REXO1 ELOABP1 KIAA1138 TCEB3BP1	Homo sapiens (human)	4	2
A0A7P0T8M7	Voltage-dependent L-type calcium channel subunit alpha	CACNA1S	Homo sapiens (human)	2	0
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
A0A186VN77	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9BUN1	Protein MENT	MENT C1orf56	Homo sapiens (human)	8	4
Q96EL2	Small ribosomal subunit protein uS3m	MRPS24	Homo sapiens (human)	0	1
A0A0J9YY54	Testis-expressed protein 13D	TEX13D	Homo sapiens (human)	0	1
P26640	Valine--tRNA ligase	VARS1 G7A VARS VARS2	Homo sapiens (human)	3	1
M9P9F2	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
A0A7I2V3V9	Cathepsin F	CTSF	Homo sapiens (human)	1	0

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