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 **12426 - 12450** 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
P19429	Troponin I, cardiac muscle	TNNI3 TNNC1	Homo sapiens (human)	1	1
P25398	Small ribosomal subunit protein eS12	RPS12	Homo sapiens (human)	1	1
Q64464	Cytochrome P450 3A13	Cyp3a13 Cyp3a-13	Mus musculus (house mouse)	0	1
Q01147	Cyclic AMP-responsive element-binding protein 1	Creb1 Creb-1	Mus musculus (house mouse)	0	1
P56182	Ribosomal RNA processing protein 1 homolog A	RRP1 D21S2056E NNP1 NOP52 RRP1A	Homo sapiens (human)	0	1
A0A0G2JW94	Clathrin interactor 1	Clint1	Rattus norvegicus (Norway rat)	0	1
Q01415	N-acetylgalactosamine kinase	GALK2 GK2	Homo sapiens (human)	0	1	bronchus cancer bronchus carcinoma dental caries dentin caries lung adenocarcinoma lung cancer lung carcinoma
V5BQU2	CTP synthase	TCDM_01016	Trypanosoma cruzi Dm28c	0	1
Q14181	DNA polymerase alpha subunit B	POLA2	Homo sapiens (human)	0	1
Q99865	Spindlin-2A	SPIN2A DXF34 SPIN2	Homo sapiens (human)	1	1
P30049	ATP synthase subunit delta, mitochondrial	ATP5F1D ATP5D	Homo sapiens (human)	0	1
P39078	T-complex protein 1 subunit delta	CCT4 ANC2 TCP4	Saccharomyces cerevisiae S288C	3	1
O95865	Putative hydrolase DDAH2	DDAH2 DDAH G6A NG30	Homo sapiens (human)	5	1
B9QPM2	Phosphodiesterase	BN1205_079680	Toxoplasma gondii VEG	0	1
P53876	Uncharacterized protein YNL184C	YNL184C	Saccharomyces cerevisiae S288C	4	1
Q6P5B5	FMR1 autosomal homolog 2	Fxr2 Fxr2h	Mus musculus (house mouse)	0	1
Q8CGA0	Protein phosphatase 1F	Ppm1f	Mus musculus (house mouse)	0	1
Q99LH1	Nucleolar GTP-binding protein 2	Gnl2	Mus musculus (house mouse)	2	1
Q9GPG3	Aminopeptidase	Psa	Drosophila melanogaster (fruit fly)	0	1
Q16394	Exostosin-1	EXT1	Homo sapiens (human)	2	1	Alzheimer's disease Cenani-Lenz syndactyly syndrome Cornelia de Lange syndrome 4 Cornelia de Lange syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Laron syndrome Legg-Calve-Perthes disease Lennox-Gastaut syndrome Leri-Weill dyschondrosteosis Maffucci syndrome Ollier disease Pick's disease Reye syndrome Ritter's disease Werner syndrome achondroplasia acute lymphoblastic leukemia adenocarcinoma adenoma adult acute lymphocytic leukemia anaplastic astrocytoma antisocial personality disorder arthritis arthropathy autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma cancer cartilage disease central nervous system cancer cerebral degeneration cervix uteri carcinoma in situ cherubism childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood leukemia chondroblastoma chondroma chondrosarcoma cleidocranial dysplasia clubfoot conduct disorder connective tissue disease cranial nerve disease cranial nerve palsy cribriform carcinoma cryoglobulinemia diabetes mellitus disease of mental health embryoma endometrial cancer endometrial carcinoma epilepsy exostosis familial hypercholesterolemia familial nephrotic syndrome fibrillary astrocytoma fibromyalgia frontotemporal dementia gallbladder disease gemistocytic astrocytoma gliosarcoma granular cell carcinoma head and neck squamous cell carcinoma hepatitis A hepatitis B hepatitis C hepatitis E hepatitis hepatocellular carcinoma hereditary multiple exostoses high grade glioma humeroradial synostosis hydrocephalus hyperostosis hypogonadism hypogonadotropic hypogonadism 7 with or without anosmia immune system disease intellectual disability juvenile myoclonic epilepsy juvenile pilocytic astrocytoma learning disability leukemia lipoid nephrosis liver cancer liver disease lupus nephritis malignant astrocytoma membranous glomerulonephritis metachondromatosis microcephaly mixed glioma mucopolysaccharidosis III mucopolysaccharidosis type IIIA multiple myeloma myositis nephrotic syndrome osteoarthritis osteonecrosis osteopoikilosis osteoporosis osteosarcoma periarthritis personality disorder pilocytic astrocytoma progeria protoplasmic astrocytoma psychotic disorder radioulnar synostosis rectal benign neoplasm rectum adenocarcinoma rectum cancer rheumatoid arthritis schizophrenia scoliosis spinal cord disease subependymal giant cell astrocytoma tendinitis thrombophilia trichorhinophalangeal syndrome type II tubular adenocarcinoma type 2 diabetes mellitus urinary tract obstruction uterine corpus cancer vasculitis vesicoureteral reflux visual epilepsy
Q9CZN7	Serine hydroxymethyltransferase, mitochondrial	Shmt2	Mus musculus (house mouse)	0	1
Q5T0F9	Coiled-coil and C2 domain-containing protein 1B	CC2D1B KIAA1836 LGD1	Homo sapiens (human)	1	1
Q9H6K1	Protein ILRUN	ILRUN C6orf106	Homo sapiens (human)	2	1
Q8IXV7	Kelch domain-containing protein 8B	KLHDC8B	Homo sapiens (human)	0	1
Q86XN6	Zinc finger protein 761	ZNF761 KIAA2033	Homo sapiens (human)	0	1

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