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 **110451 - 110475** of **126547** in total

« First

‹ Prev

…

4415

4416

4417

4418

4419

4420

4421

4422

4423

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
P42208	Septin-2	Septin2 Nedd5 Sept2	Mus musculus (house mouse)	0	1
Q9NRM7	Serine/threonine-protein kinase LATS2	LATS2 KPM	Homo sapiens (human)	8	1
Q9GZZ9	Ubiquitin-like modifier-activating enzyme 5	UBA5 UBE1DC1	Homo sapiens (human)	0	1
Q8WXD9	Caskin-1	CASKIN1 KIAA1306	Homo sapiens (human)	2	1
Q9NPA3	Mid1-interacting protein 1	MID1IP1 MIG12	Homo sapiens (human)	0	1
P86176	T-cell immunoreceptor with Ig and ITIM domains	Tigit Vstm3	Mus musculus (house mouse)	2	1
O75038	1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase eta-2	PLCH2 KIAA0450 PLCL4	Homo sapiens (human)	1	1	azoospermia intellectual disability learning disability schizophrenia
P06399	Fibrinogen alpha chain	Fga	Rattus norvegicus (Norway rat)	1	1
Q6NYB7	Ras-related protein Rab-1A	Rab1A Rab1	Rattus norvegicus (Norway rat)	0	1
A0A5F9D539	PDZ and LIM domain 5	PDLIM5	Oryctolagus cuniculus (rabbit)	0	1
P83436	Conserved oligomeric Golgi complex subunit 7	COG7	Homo sapiens (human)	1	1	Cauda equina syndrome Laron syndrome achondroplasia autosomal recessive congenital ichthyosis 10 autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis 2 autosomal recessive congenital ichthyosis 3 autosomal recessive congenital ichthyosis 4A autosomal recessive congenital ichthyosis 5 autosomal recessive congenital ichthyosis 6 autosomal recessive congenital ichthyosis 7 autosomal recessive congenital ichthyosis 8 autosomal recessive congenital ichthyosis 9 autosomal recessive congenital ichthyosis cardiomyopathy cerebral degeneration congenital disorder of glycosylation type II congenital disorder of glycosylation type IIe congenital disorder of glycosylation congenital heart disease congestive heart failure endomyocardial fibrosis esophagitis familial hypertrophic cardiomyopathy gastroesophageal reflux disease hydronephrosis hypertrichosis hypertrophic cardiomyopathy hypoglycemia isolated elevated serum creatine phosphokinase levels microcephaly neurogenic bladder obsolete congenital ichthyosiform erythroderma peptic esophagitis placental insufficiency sensorineural hearing loss
Q99598	Translin-associated protein X	TSNAX TRAX	Homo sapiens (human)	0	1
Q9C091	GREB1-like protein	GREB1L C18orf6 KIAA1772	Homo sapiens (human)	0	1
Q9NSD9	Phenylalanine--tRNA ligase beta subunit	FARSB FARSLB FRSB	Homo sapiens (human)	0	1
Q9Y305	Acyl-coenzyme A thioesterase 9, mitochondrial	ACOT9	Homo sapiens (human)	0	1
O08599	Syntaxin-binding protein 1	Stxbp1	Mus musculus (house mouse)	5	1
Q9H582	Zinc finger protein 644	ZNF644 KIAA1221 ZEP2	Homo sapiens (human)	3	1
Q9LZQ7	At3g62330	T12C14_30	Arabidopsis thaliana (thale cress)	0	1
Q15785	Mitochondrial import receptor subunit TOM34	TOMM34 URCC3	Homo sapiens (human)	0	1
V5BP71	Uncharacterized protein	TCDM_01562	Trypanosoma cruzi Dm28c	0	1
Q9BYD6	Large ribosomal subunit protein uL1m	MRPL1	Homo sapiens (human)	0	1
Q6NUN7	Jhy protein homolog	JHY C11orf63	Homo sapiens (human)	0	1
Q5FWH3	Grainyhead-like protein 3 homolog	Grhl3 Get1 Som Tfcp2l4	Mus musculus (house mouse)	0	1
Q04758	cAMP-dependent protein kinase inhibitor beta	Pkib	Mus musculus (house mouse)	1	1
Q14028	Cyclic nucleotide-gated channel beta-1	CNGB1 CNCG2 CNCG3L CNCG4 RCNC2	Homo sapiens (human)	1	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements