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 **111276 - 111300** of **126547** in total

« First

‹ Prev

…

4448

4449

4450

4451

4452

4453

4454

4455

4456

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q9QZ76	Myoglobin	Mb	Rattus norvegicus (Norway rat)	0	1
Q92903	Phosphatidate cytidylyltransferase 1	CDS1 CDS	Homo sapiens (human)	1	1	B-cell lymphoma appendicitis arachnoiditis bipolar disorder breast cancer cancer carcinoma carotid stenosis chondrosarcoma colorectal cancer colorectal carcinoma congestive heart failure depressive disorder diffuse large B-cell lymphoma embryoma exanthema subitum eye disease giant cell glioblastoma glioblastoma high grade glioma large intestine cancer meningitis milker's nodule myasthenia gravis obsolete ymphosarcoma panic disorder sarcomatoid carcinoma substance abuse substance-related disorder temporal arteritis variola major
Q9Y3T6	R3H and coiled-coil domain-containing protein 1	R3HCC1	Homo sapiens (human)	0	1
Q6P9G9	Zinc finger protein 449	ZNF449 ZSCAN19	Homo sapiens (human)	1	1
A0A1P8B7E4	BEL1-like homeodomain 2	BLH2 AP22.90 AP22_90 BEL1-like homeodomain 2 SAW1 SAWTOOTH 1	Arabidopsis thaliana (thale cress)	0	1
Q9C093	Sperm flagellar protein 2	SPEF2 KIAA1770 KPL2	Homo sapiens (human)	0	1
D4A0B4	Ankyrin repeat domain 17	Ankrd17	Rattus norvegicus (Norway rat)	0	1
Q4CRR1	Present in the outer mitochondrial membrane proteome 10	Tc00.1047053508083.10	Trypanosoma cruzi strain CL Brener	0	1
B1AVZ0	Uracil phosphoribosyltransferase homolog	Uprt	Mus musculus (house mouse)	0	1
P39678	Transcription factor MBP1	MBP1	Saccharomyces cerevisiae S288C	4	1
A0A384L4P3	Uncharacterized protein	At3g61690	Arabidopsis thaliana (thale cress)	0	1
Q96BI3	Gamma-secretase subunit APH-1A	APH1A PSF	Homo sapiens (human)	0	1
Q5JVF3	PCI domain-containing protein 2	PCID2	Homo sapiens (human)	0	1
P39935	Eukaryotic initiation factor 4F subunit p150	TIF4631	Saccharomyces cerevisiae S288C	18	1
P19246	Neurofilament heavy polypeptide	Nefh Kiaa0845 Nfh	Mus musculus (house mouse)	4	1
Q4CW22	DNA/RNA-binding protein Alba-like domain-containing protein	Tc00.1047053504001.20	Trypanosoma cruzi strain CL Brener	0	1
Q9Z1K5	E3 ubiquitin-protein ligase ARIH1	Arih1 Ari Ubch7bp Uip77	Mus musculus (house mouse)	0	1
Q6ZQJ9	Condensin complex subunit 2 (Fragment)	Ncaph Brrn1 mKIAA0074	Mus musculus (house mouse)	0	1
P32189	Glycerol kinase	GK	Homo sapiens (human)	1	1	Aland Island eye disease Becker muscular dystrophy Duchenne muscular dystrophy Kallmann syndrome Klinefelter syndrome Laron syndrome Patau syndrome Sheehan syndrome X-linked adrenal hypoplasia congenita achondroplasia 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 chromosome Xp21 deletion syndrome cone-rod dystrophy congenital muscular dystrophy coronary artery disease diabetes mellitus distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hypercholesterolemia fundus albipunctatus galactokinase deficiency galactosemia glycerol kinase deficiency hypertropia hypoglycemia hypogonadism hypogonadotropic hypogonadism 1 with or without anosmia hypogonadotropic hypogonadism 10 with or without anosmia hypogonadotropic hypogonadism 11 with or without anosmia hypogonadotropic hypogonadism 12 with or without anosmia hypogonadotropic hypogonadism 13 with or without anosmia hypogonadotropic hypogonadism 14 with or without anosmia hypogonadotropic hypogonadism 16 with or without anosmia hypogonadotropic hypogonadism 17 with or without anosmia hypogonadotropic hypogonadism 18 with or without anosmia hypogonadotropic hypogonadism 19 with or without anosmia hypogonadotropic hypogonadism 2 with or without anosmia hypogonadotropic hypogonadism 20 with or without anosmia hypogonadotropic hypogonadism 21 with or without anosmia hypogonadotropic hypogonadism 22 with or without anosmia hypogonadotropic hypogonadism 3 with or without anosmia hypogonadotropic hypogonadism 4 with or without anosmia hypogonadotropic hypogonadism 5 with or without anosmia hypogonadotropic hypogonadism 6 with or without anosmia hypogonadotropic hypogonadism 7 with or without anosmia hypogonadotropic hypogonadism 8 with or without anosmia hypogonadotropic hypogonadism 9 with or without anosmia hypogonadotropic hypogonadism hypopituitarism intellectual disability isolated growth hormone deficiency type IA isolated growth hormone deficiency type IB isolated growth hormone deficiency type II isolated growth hormone deficiency type III isolated growth hormone deficiency learning disability limb-girdle muscular dystrophy mechanical strabismus muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 obesity 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 oculopharyngeal muscular dystrophy ophthalmoplegia osteoporosis panhypopituitarism placental insufficiency retinitis pigmentosa rippling muscle disease 2 strabismus tuberculosis type 2 diabetes mellitus
Q94547	Regulator of gene activity	Rga Not2	Drosophila melanogaster (fruit fly)	0	1
Q12051	Geranylgeranyl pyrophosphate synthase BTS1	BTS1	Saccharomyces cerevisiae S288C	1	1
Q8WVZ7	E3 ubiquitin-protein ligase RNF133	RNF133	Homo sapiens (human)	2	1
O15726	Casein kinase I	CK1	Plasmodium falciparum Dd2	0	1
P47884	Olfactory receptor 1D4	OR1D4	Homo sapiens (human)	2	1
Q8N111	Cell cycle exit and neuronal differentiation protein 1	CEND1 BM88	Homo sapiens (human)	2	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements