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 **15626 - 15650** 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
V5D8L4	Cleavage and polyadenylation specificity factor 30 kDa subunit	TCDM_08235	Trypanosoma cruzi Dm28c	0	1
Q4DSZ1	HECT domain-containing protein	Tc00.1047053504769.70	Trypanosoma cruzi strain CL Brener	0	1
Q13885	Tubulin beta-2A chain	TUBB2A TUBB2	Homo sapiens (human)	6	1
A0A178ULB6	RXT3-like protein	AXX17_At5g08310	Arabidopsis thaliana (thale cress)	0	1
Q8IYJ2	Uncharacterized protein C10orf67, mitochondrial	C10orf67 LINC01552	Homo sapiens (human)	0	1
Q06330	Recombining binding protein suppressor of hairless	RBPJ IGKJRB IGKJRB1 RBPJK RBPSUH	Homo sapiens (human)	2	1
Q00080	Elongation factor 1-alpha	MEF-1	Plasmodium falciparum K1	0	1
Q8BMS1	Trifunctional enzyme subunit alpha, mitochondrial	Hadha	Mus musculus (house mouse)	0	1
Q9CXW4	Large ribosomal subunit protein uL5	Rpl11	Mus musculus (house mouse)	0	1
Q61188	Histone-lysine N-methyltransferase EZH2	Ezh2 Enx1h	Mus musculus (house mouse)	1	1
P00366	Glutamate dehydrogenase 1, mitochondrial	GLUD1 GLUD	Bos taurus (cattle)	0	1
Q86TL2	Store-operated calcium entry regulator STIMATE	STIMATE TMEM110	Homo sapiens (human)	2	1
Q92562	Polyphosphoinositide phosphatase	FIG4 KIAA0274 SAC3	Homo sapiens (human)	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
Q9S840	Squamosa promoter-binding-like protein 2	SPL2	Arabidopsis thaliana (thale cress)	0	1
A6NKT7	RanBP2-like and GRIP domain-containing protein 3	RGPD3 RGP3	Homo sapiens (human)	2	1
A2AIM4	Tropomyosin beta chain	Tpm2	Mus musculus (house mouse)	0	1
P50750	Cyclin-dependent kinase 9	CDK9 CDC2L4 TAK	Homo sapiens (human)	0	1
Q9BXL5	Hemogen	HEMGN EDAG NDR	Homo sapiens (human)	0	1
P27515	Uridine kinase	URK1	Saccharomyces cerevisiae S288C	2	1
Q8TC92	Ecto-NOX disulfide-thiol exchanger 1	ENOX1	Homo sapiens (human)	1	1
Q96EY8	Corrinoid adenosyltransferase MMAB	MMAB	Homo sapiens (human)	2	1
Q02080	Myocyte-specific enhancer factor 2B	MEF2B XMEF2	Homo sapiens (human)	0	1
Q924H7	WW domain-containing adapter protein with coiled-coil	Wac Kiaa1844	Mus musculus (house mouse)	3	1
Q9Y3P9	Rab GTPase-activating protein 1	RABGAP1	Homo sapiens (human)	0	1
P50273	Mitochondrial translation factor ATP22	ATP22 TCM10	Saccharomyces cerevisiae S288C	1	1

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