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 **4501 - 4525** of **126547** in total

« First

‹ Prev

…

177

178

179

180

181

182

183

184

185

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
P32883	GTPase KRas	Kras Kras2	Mus musculus (house mouse)	1	2
Q6A058	Armadillo repeat-containing X-linked protein 2	Armcx2 Kiaa0512	Mus musculus (house mouse)	6	2
P63261	Actin, cytoplasmic 2	ACTG1 ACTG	Homo sapiens (human)	10	2
Q15075	Early endosome antigen 1	EEA1 ZFYVE2	Homo sapiens (human)	4	2
Q9Y2B1	Ribitol-5-phosphate xylosyltransferase 1	RXYLT1 TMEM5	Homo sapiens (human)	4	2	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Turner syndrome Walker-Warburg syndrome autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy cataract coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A10 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism distal myopathy epilepsy facioscapulohumeral muscular dystrophy fundus dystrophy glaucoma gonadal dysgenesis hydranencephaly hydrocephalus intellectual disability learning disability limb-girdle muscular dystrophy lissencephaly microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obstructive hydrocephalus oculopharyngeal muscular dystrophy optic atrophy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly syndromic X-linked intellectual disability Najm type visual epilepsy
Q16204	Coiled-coil domain-containing protein 6	CCDC6 D10S170 TST1	Homo sapiens (human)	5	2
Q9BPX7	UPF0415 protein C7orf25	C7orf25	Homo sapiens (human)	1	2
O15409	Forkhead box protein P2	FOXP2 CAGH44 TNRC10	Homo sapiens (human)	2	2
O60610	Protein diaphanous homolog 1	DIAPH1 DIAP1	Homo sapiens (human)	6	2
P55010	Eukaryotic translation initiation factor 5	EIF5	Homo sapiens (human)	2	2
Q04941	Proteolipid protein 2	PLP2 A4	Homo sapiens (human)	5	2
P99027	Large ribosomal subunit protein P2	Rplp2	Mus musculus (house mouse)	4	2
Q8VD65	Phosphoinositide 3-kinase regulatory subunit 4	Pik3r4 Vps15	Mus musculus (house mouse)	4	2
Q96RK0	Protein capicua homolog	CIC KIAA0306	Homo sapiens (human)	36	2
Q9R0N7	Synaptotagmin-7	Syt7	Mus musculus (house mouse)	1	2
Q63155	Netrin receptor DCC	Dcc	Rattus norvegicus (Norway rat)	7	2
O60244	Mediator of RNA polymerase II transcription subunit 14	MED14 ARC150 CRSP2 CXorf4 DRIP150 EXLM1 RGR1 TRAP170	Homo sapiens (human)	3	2
P25976	Nucleolar transcription factor 1	Ubtf Tcfubf Ubf-1 Ubf1	Mus musculus (house mouse)	1	2
Q63959	Potassium voltage-gated channel subfamily C member 3	Kcnc3	Mus musculus (house mouse)	3	2
Q91VS8	FERM, ARHGEF and pleckstrin domain-containing protein 2	Farp2 Kiaa0793	Mus musculus (house mouse)	2	2
Q8VC42	Regulator of MON1-CCZ1 complex	Rmc1 Mic1 Wdr98	Mus musculus (house mouse)	1	2
Q91Z53	Glyoxylate reductase/hydroxypyruvate reductase	Grhpr Glxr	Mus musculus (house mouse)	1	2
Q6NYC8	Phostensin	PPP1R18 HKMT1098 KIAA1949	Homo sapiens (human)	4	2
P62304	Small nuclear ribonucleoprotein E	SNRPE	Homo sapiens (human)	1	2
A2ATK9	Family with sequence similarity 171, member A1	Fam171a1	Mus musculus (house mouse)	2	2

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements