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 **1876 - 1900** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
P14854	Cytochrome c oxidase subunit 6B1	COX6B1 COX6B	Homo sapiens (human)	1
Q9NRY2	SOSS complex subunit C	INIP C9orf80 SSBIP1	Homo sapiens (human)	1
P55055	Oxysterols receptor LXR-beta	NR1H2 LXRB NER UNR	Homo sapiens (human)	1
P52298	Nuclear cap-binding protein subunit 2	NCBP2 CBP20	Homo sapiens (human)	1
Q9NQ29	Putative RNA-binding protein Luc7-like 1	LUC7L LUC7L1	Homo sapiens (human)	1
Q96HS1	Serine/threonine-protein phosphatase PGAM5, mitochondrial	PGAM5	Homo sapiens (human)	1
Q13630	GDP-L-fucose synthase	GFUS SDR4E1 TSTA3	Homo sapiens (human)	1
O43747	AP-1 complex subunit gamma-1	AP1G1 ADTG CLAPG1	Homo sapiens (human)	1
Q6PEY2	Tubulin alpha-3E chain	TUBA3E	Homo sapiens (human)	1
P11217	Glycogen phosphorylase, muscle form	PYGM	Homo sapiens (human)	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
Q9H3P7	Golgi resident protein GCP60	ACBD3 GCP60 GOCAP1 GOLPH1	Homo sapiens (human)	1
Q9C0G0	Zinc finger protein 407	ZNF407 KIAA1703	Homo sapiens (human)	1
Q99733	Nucleosome assembly protein 1-like 4	NAP1L4 NAP2	Homo sapiens (human)	1
Q15773	Myeloid leukemia factor 2	MLF2	Homo sapiens (human)	1
P05423	DNA-directed RNA polymerase III subunit RPC4	POLR3D BN51 BN51T	Homo sapiens (human)	1
O95935	T-box transcription factor TBX18	TBX18	Homo sapiens (human)	1
P32320	Cytidine deaminase	CDA CDD	Homo sapiens (human)	1
Q9HCI6	E3 SUMO-protein ligase KIAA1586	KIAA1586	Homo sapiens (human)	1
P61960	Ubiquitin-fold modifier 1	UFM1 C13orf20	Homo sapiens (human)	1
F8VR77	Proliferation-associated 2G4	PA2G4	Homo sapiens (human)	1
O76083	High affinity cGMP-specific 3',5'-cyclic phosphodiesterase 9A	PDE9A	Homo sapiens (human)	1
O75794	Translation initiation factor eIF2 assembly protein	CDC123 C10orf7 D123	Homo sapiens (human)	1
P01599	Immunoglobulin kappa variable 1-17	IGKV1-17	Homo sapiens (human)	1
P07101	Tyrosine 3-monooxygenase	TH TYH	Homo sapiens (human)	1
Q9H2M9	Rab3 GTPase-activating protein non-catalytic subunit	RAB3GAP2 KIAA0839	Homo sapiens (human)	1

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