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 **3226 - 3250** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
Q9NXH9	tRNA (guanine(26)-N(2))-dimethyltransferase	TRMT1	Homo sapiens (human)	1
Q8WUQ7	Splicing factor Cactin	CACTIN C19orf29	Homo sapiens (human)	1
Q5SRE7	Phytanoyl-CoA dioxygenase domain-containing protein 1	PHYHD1	Homo sapiens (human)	1
P48436	Transcription factor SOX-9	SOX9	Homo sapiens (human)	1
Q9BQG1	Synaptotagmin-3	SYT3	Homo sapiens (human)	1
O43716	Glutamyl-tRNA(Gln) amidotransferase subunit C, mitochondrial	GATC 15E1.2	Homo sapiens (human)	1
Q02386	Zinc finger protein 45	ZNF45 KOX5 ZNF13	Homo sapiens (human)	1
P62277	Small ribosomal subunit protein uS15	RPS13	Homo sapiens (human)	1
Q32MH5	Atos homolog protein A	ATOSA FAM214A KIAA1370	Homo sapiens (human)	1
Q9HD67	Unconventional myosin-X	MYO10 KIAA0799	Homo sapiens (human)	1
Q13542	Eukaryotic translation initiation factor 4E-binding protein 2	EIF4EBP2	Homo sapiens (human)	1
A0AVI2	Fer-1-like protein 5	FER1L5	Homo sapiens (human)	1
P23193	Transcription elongation factor A protein 1	TCEA1 GTF2S TFIIS	Homo sapiens (human)	1
Q02641	Voltage-dependent L-type calcium channel subunit beta-1	CACNB1 CACNLB1	Homo sapiens (human)	1
Q969F2	Protein naked cuticle homolog 2	NKD2	Homo sapiens (human)	1
Q8N0T1	Ribosomal biogenesis factor	RBIS C8orf59	Homo sapiens (human)	1
Q92530	Proteasome inhibitor PI31 subunit	PSMF1	Homo sapiens (human)	1
P25685	DnaJ homolog subfamily B member 1	DNAJB1 DNAJ1 HDJ1 HSPF1	Homo sapiens (human)	1
Q9Y2S2	Lambda-crystallin homolog	CRYL1 CRY	Homo sapiens (human)	1	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Laron syndrome Pick's disease Reye syndrome T-cell acute lymphoblastic leukemia Zollinger-Ellison syndrome achondroplasia acquired thrombocytopenia acute biphenotypic leukemia acute leukemia acute myeloid leukemia autoimmune disease autoimmune lymphoproliferative syndrome beta thalassemia breast cancer breast carcinoma cancer cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cerebral degeneration cholangiocarcinoma diabetes insipidus diarrhea embryoma giardiasis hepatocellular carcinoma hyperinsulinism hypoglycemia immune system disease intrahepatic cholangiocarcinoma liver cancer liver carcinoma mood disorder neurohypophyseal diabetes insipidus perinatal necrotizing enterocolitis placental insufficiency primary hyperoxaluria prostate cancer prostate carcinoma thalassemia
P21283	V-type proton ATPase subunit C 1	ATP6V1C1 ATP6C ATP6D VATC	Homo sapiens (human)	1
Q9Y6A4	Cilia- and flagella-associated protein 20	CFAP20 BUG22 C16orf80 GTL3	Homo sapiens (human)	1
Q9BY27	Protein DGCR6L	DGCR6L	Homo sapiens (human)	1
Q70EK9	Ubiquitin carboxyl-terminal hydrolase 51	USP51	Homo sapiens (human)	1
P29218	Inositol monophosphatase 1	IMPA1 IMPA	Homo sapiens (human)	1	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Duchenne muscular dystrophy Lewy body dementia Pick's disease Reye syndrome alcohol dependence alcohol use disorder antisocial personality disorder aplastic anemia 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 avoidant personality disorder bipolar disorder brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cardiovascular system disease central nervous system cancer cerebral artery occlusion cerebral atherosclerosis cerebral degeneration cerebral infarction cerebrovascular disease chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cone-rod dystrophy congenital muscular dystrophy conjunctivitis cryptosporidiosis cystitis delusional disorder dermatophytosis diabetes mellitus distal myopathy embryoma epilepsy essential hypertension facioscapulohumeral muscular dystrophy focal epilepsy fundus albipunctatus fungal infectious disease gallbladder disease gliosarcoma glycogen storage disease IV glycogen storage disease VI glycogen storage disease VII heart disease high grade glioma hypertension intellectual disability intracranial arteriosclerosis large intestine cancer learning disability limb-girdle muscular dystrophy liver disease lung benign neoplasm lung cancer lung carcinoma mixed glioma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 narcissistic personality disorder 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 ovarian cancer ovarian carcinoma paranoid schizophrenia partial motor epilepsy primary pulmonary hypertension retinitis pigmentosa rippling muscle disease 2 sickle cell anemia syndromic X-linked intellectual disability 94 systemic primary carnitine deficiency disease trigonitis type 2 diabetes mellitus visual epilepsy
Q7RTR2	NLR family CARD domain-containing protein 3	NLRC3 NOD3	Homo sapiens (human)	1

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