GlyCosmos Portal

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The O-GlcNAc Database	June 3, 2024
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Displaying entries **1201 - 1225** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
Q14195	Dihydropyrimidinase-related protein 3	DPYSL3 CRMP4 DRP3 ULIP ULIP1	Homo sapiens (human)	1
Q6NX45	Zinc finger protein 774	ZNF774	Homo sapiens (human)	1
Q4VC31	Protein MIX23	MIX23 CCDC58	Homo sapiens (human)	1
P06746	DNA polymerase beta	POLB	Homo sapiens (human)	1
P62081	Small ribosomal subunit protein eS7	RPS7	Homo sapiens (human)	1
Q9Y3D3	Small ribosomal subunit protein bS16m	MRPS16 RPMS16	Homo sapiens (human)	1
O96007	Molybdopterin synthase catalytic subunit	MOCS2 MCBPE MOCO1	Homo sapiens (human)	1
Q9UHB9	Signal recognition particle subunit SRP68	SRP68	Homo sapiens (human)	1
O43396	Thioredoxin-like protein 1	TXNL1 TRP32 TXL TXNL	Homo sapiens (human)	1
Q9UFW8	CGG triplet repeat-binding protein 1	CGGBP1 CGGBP	Homo sapiens (human)	1
Q8WTS1	1-acylglycerol-3-phosphate O-acyltransferase ABHD5	ABHD5 NCIE2	Homo sapiens (human)	1
Q8TBR4	Putative STAG3-like protein 4	STAG3L4	Homo sapiens (human)	1
Q96H79	Zinc finger CCCH-type antiviral protein 1-like	ZC3HAV1L C7orf39	Homo sapiens (human)	1
P29597	Non-receptor tyrosine-protein kinase TYK2	TYK2	Homo sapiens (human)	1
Q69YN2	CWF19-like protein 1	CWF19L1	Homo sapiens (human)	1
O00194	Ras-related protein Rab-27B	RAB27B	Homo sapiens (human)	1
Q5T8I9	Small RNA 2'-O-methyltransferase	HENMT1 C1orf59	Homo sapiens (human)	1
Q8IZ69	tRNA (uracil-5-)-methyltransferase homolog A	TRMT2A	Homo sapiens (human)	1
Q9Y228	TRAF3-interacting JNK-activating modulator	TRAF3IP3 T3JAM	Homo sapiens (human)	1
Q68DU8	BTB/POZ domain-containing protein KCTD16	KCTD16 KIAA1317	Homo sapiens (human)	1
P05204	Non-histone chromosomal protein HMG-17	HMGN2 HMG17	Homo sapiens (human)	1
F2Z3F1	Uncharacterized protein C5orf67	C5orf67	Homo sapiens (human)	1
P31689	DnaJ homolog subfamily A member 1	DNAJA1 DNAJ2 HDJ2 HSJ2 HSPF4	Homo sapiens (human)	1
Q96FQ6	Protein S100-A16	S100A16 S100F	Homo sapiens (human)	1
P43034	Platelet-activating factor acetylhydrolase IB subunit beta	PAFAH1B1 LIS1 MDCR MDS PAFAHA	Homo sapiens (human)	1	3p deletion syndrome Alzheimer's disease Angelman syndrome B-cell lymphoma Behcet's disease Crohn's colitis Crohn's disease Ewing sarcoma Gaucher's disease type I Gaucher's disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Joubert syndrome Langerhans-cell histiocytosis Marfan syndrome Miller-Dieker lissencephaly syndrome NFIA-related disorder Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease REM sleep behavior disorder Rett syndrome SATB2-associated syndrome Shwachman-Diamond syndrome Smith-Magenis syndrome West syndrome X-linked juvenile retinoschisis 1 Zellweger syndrome acute monocytic leukemia acute myeloid leukemia adult medulloblastoma adult respiratory distress syndrome aggressive periodontitis allergic asthma alternating hemiplegia of childhood anxiety disorder aplastic anemia asthma autism spectrum disorder autistic disorder autonomic neuropathy bone marrow cancer bone osteosarcoma bronchus cancer bronchus carcinoma cancer central nervous system disease childhood acute myeloid leukemia childhood leukemia childhood medulloblastoma childhood osteosarcoma chromophobe renal cell carcinoma chromosome 13q14 deletion syndrome chromosome 15q13.3 microdeletion syndrome chromosome 15q24 deletion syndrome chromosome 15q26-qter deletion syndrome chromosome 16p11.2 deletion syndrome, 220-kb chromosome 16p12.2-p11.2 deletion syndrome chromosome 17p13.1 deletion syndrome chromosome 17p13.3 duplication syndrome chromosome 17q12 deletion syndrome chromosome 17q23.1-q23.2 deletion syndrome chromosome 18q deletion syndrome chromosome 1q21.1 deletion syndrome chromosome 1q41-q42 deletion syndrome chromosome 2p16.1-p15 deletion syndrome chromosome 6pter-p24 deletion syndrome chromosome 8q21.11 deletion syndrome chromosome 9p deletion syndrome chronic monocytic leukemia chronic myelomonocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congestive heart failure cortical dysplasia-focal epilepsy syndrome dementia depressive disorder distal 10q deletion syndrome distal arthrogryposis dysthymic disorder dystonia embryoma epilepsy essential thrombocythemia essential tremor familial adenomatous polyposis 1 familial adenomatous polyposis generalized anxiety disorder giant cell glioblastoma glioblastoma glomerulonephritis hematologic cancer hepatocellular carcinoma high grade glioma hydranencephaly hydrocephalus impulse control disorder inclusion body myositis inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intermittent explosive disorder intrinsic asthma islet cell tumor juvenile myelomonocytic leukemia kidney disease kleptomania late onset Parkinson's disease learning disability leukemia lingual-facial-buccal dyskinesia lissencephaly liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma microcephaly mood disorder movement disease multiple myeloma multiple system atrophy myelodysplastic syndrome myelodysplastic/myeloproliferative neoplasm myeloproliferative neoplasm nephritis nephrosis nervous system disease neurotic disorder newborn respiratory distress syndrome non-Hodgkin lymphoma nonpapillary renal cell carcinoma obsolete constipation obsolete infantile epileptic encephalopathy obsolete melancholia obsolete ymphosarcoma obstructive hydrocephalus oculocerebrorenal syndrome omphalocele osteosarcoma papillary renal cell carcinoma periodontosis periventricular nodular heterotopia peroxisome biogenesis disorder 1A phobic disorder polycystic ovary syndrome polyhydramnios pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 postural orthostatic tachycardia syndrome progressive supranuclear palsy psychotic disorder pyoureter renal carcinoma renal cell carcinoma reticulosarcoma retinitis pigmentosa 13 sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder secondary Parkinson disease senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus speech disorder subcortical band heterotopia syndromic X-linked intellectual disability Najm type trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis ulcerative colitis umbilical hernia vascular disease visual epilepsy

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