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 **14426 - 14450** 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
Q9FIA3	Gb\|AAF16663.1	At5g55040	Arabidopsis thaliana (thale cress)	0	1
O43747	AP-1 complex subunit gamma-1	AP1G1 ADTG CLAPG1	Homo sapiens (human)	0	1
Q4DXX9	ABC transporter, putative	Tc00.1047053510431.150	Trypanosoma cruzi strain CL Brener	0	1
Q6PEY2	Tubulin alpha-3E chain	TUBA3E	Homo sapiens (human)	0	1
Q99666	RANBP2-like and GRIP domain-containing protein 5/6	RGPD5 RGPD6 RANBP2L1 RANBP2L2 RGP5 RGP6 RGP7 RGPD7	Homo sapiens (human)	2	1
Q6P4T2	U5 small nuclear ribonucleoprotein 200 kDa helicase	Snrnp200 Kiaa0788	Mus musculus (house mouse)	1	1
Q4DMX9	3-hydroxyisobutyryl-CoA hydrolase	Tc00.1047053511529.160	Trypanosoma cruzi strain CL Brener	0	1
P11217	Glycogen phosphorylase, muscle form	PYGM	Homo sapiens (human)	0	1	Gerstmann-Straussler-Scheinker syndrome Gorham's disease Peutz-Jeghers syndrome X-linked myopathy with excessive autophagy 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 bacterial sepsis breast cancer breast carcinoma cancer carcinoma cholestasis coronary artery disease cystinuria disease of metabolism distal myopathy facioscapulohumeral muscular dystrophy familial adenomatous polyposis familial periodic paralysis galactosemia gastrinoma glucosephosphate dehydrogenase deficiency glycogen storage disease IV glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease V glycogen storage disease VI glycogen storage disease VII glycogen storage disease gout head and neck squamous cell carcinoma insulinoma invasive lobular carcinoma islet cell tumor isolated elevated serum creatine phosphokinase levels kidney failure limb-girdle muscular dystrophy lipoma melanoma multiple endocrine neoplasia type 1 multiple symmetric lipomatosis muscular dystrophy myoglobinuria myopathy 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 pleomorphic lipoma pre-eclampsia pseudosarcomatous fibromatosis sarcomatoid carcinoma skin melanoma vitelliform macular dystrophy von Hippel-Lindau disease
Q02094	Ammonium transporter Rh type A	RHAG RH50	Homo sapiens (human)	3	1
O35826	Bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase	Gne Glcne	Rattus norvegicus (Norway rat)	0	1
Q9H3P7	Golgi resident protein GCP60	ACBD3 GCP60 GOCAP1 GOLPH1	Homo sapiens (human)	0	1
Q9C0G0	Zinc finger protein 407	ZNF407 KIAA1703	Homo sapiens (human)	0	1
Q9SV55	AFP homolog 2	AFPH2 NINJA	Arabidopsis thaliana (thale cress)	0	1
Q99733	Nucleosome assembly protein 1-like 4	NAP1L4 NAP2	Homo sapiens (human)	0	1
K2N9B5	Extracellular receptor, putative	MOQ_004739	Trypanosoma cruzi marinkellei	0	1
P25567	RNA-binding protein SRO9	SRO9	Saccharomyces cerevisiae S288C	7	1
P18085	ADP-ribosylation factor 4	ARF4 ARF2	Homo sapiens (human)	3	1	Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome autosomal dominant polycystic kidney disease breast cancer cystic kidney disease giant cell glioblastoma glioblastoma hepatitis C high grade glioma ovarian cancer ovarian carcinoma
Q15773	Myeloid leukemia factor 2	MLF2	Homo sapiens (human)	0	1
D3Z2B3	Acyl-Coenzyme A dehydrogenase family, member 12	Acad12	Mus musculus (house mouse)	0	1
P05423	DNA-directed RNA polymerase III subunit RPC4	POLR3D BN51 BN51T	Homo sapiens (human)	0	1
Q4DQ37	RNA helicase	Tc00.1047053511825.180	Trypanosoma cruzi strain CL Brener	0	1
Q6ZNL6	FYVE, RhoGEF and PH domain-containing protein 5	FGD5 ZFYVE23	Homo sapiens (human)	3	1
Q9C0E4	Glutamate receptor-interacting protein 2	GRIP2 KIAA1719	Homo sapiens (human)	2	1
F4I982	GYF domain-containing protein	At1g24300	Arabidopsis thaliana (thale cress)	0	1
P04692	Tropomyosin alpha-1 chain	Tpm1 Alpha-tm Tpma	Rattus norvegicus (Norway rat)	5	1

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