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 **15226 - 15250** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q9UPT6	C-Jun-amino-terminal kinase-interacting protein 3	MAPK8IP3 JIP3 KIAA1066	Homo sapiens (human)	1	2
Q9UIA9	Exportin-7	XPO7 KIAA0745 RANBP16	Homo sapiens (human)	1	2
Q8NBU5	Outer mitochondrial transmembrane helix translocase	ATAD1	Homo sapiens (human)	1	2
Q13613	Myotubularin-related protein 1	MTMR1	Homo sapiens (human)	2	2	Charcot-Marie-Tooth disease type 4B1 centronuclear myopathy X-linked centronuclear myopathy congenital structural myopathy myotonic dystrophy type 1 myotonic dystrophy type 2
P57071	PR domain zinc finger protein 15	PRDM15 C21orf83 ZNF298	Homo sapiens (human)	1	2
Q8N967	Leucine-rich repeat and transmembrane domain-containing protein 2	LRTM2	Homo sapiens (human)	5	2
Q15125	3-beta-hydroxysteroid-Delta(8),Delta(7)-isomerase	EBP	Homo sapiens (human)	3	2	Alzheimer's disease Balo concentric sclerosis Dandy-Walker syndrome Klinefelter syndrome Klippel-Feil syndrome Krabbe disease Laron syndrome Marfan syndrome Patau syndrome Peters anomaly Sjogren-Larsson syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 X-linked cleft palate with or without ankyloglossia achondroplasia actinic keratosis acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute promyelocytic leukemia adrenoleukodystrophy adult fibrosarcoma allergic asthma alopecia ankyloglossia aortic valve disease 2 aortic valve stenosis arteriosclerotic cardiovascular disease asthma atherosclerosis atypical chronic myeloid leukemia, BCR-ABL1 negative autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome autosomal dominant chondrodysplasia punctata autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis bladder carcinoma brain stem infarction breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cartilage-hair hypoplasia cataract central nervous system cancer central nervous system disease cerebral artery occlusion cerebral infarction cerebrovascular disease childhood acute myeloid leukemia childhood leukemia chondrodysplasia punctata choriocarcinoma chromophobe renal cell carcinoma chronic monocytic leukemia chronic myeloid leukemia clear cell renal cell carcinoma cleft palate clubfoot collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma communicating hydrocephalus congenital heart disease congenital nystagmus congenital ptosis congestive heart failure cornea plana coronary artery disease cryptorchidism cystic fibrosis dementia diabetes mellitus dissociated nystagmus embryoma epilepsy essential hypertension essential thrombocythemia familial retinoblastoma fibrosarcoma gastrointestinal system cancer giant cell glioblastoma glaucoma glioblastoma gliosarcoma granuloma annulare hematologic cancer hemophilia B hepatitis B hepatitis C hepatocellular carcinoma high grade glioma hydrocephalus hydronephrosis hyperostosis hypertension ichthyosis intellectual disability intrinsic asthma isolated cleft palate keratosis follicularis kidney failure large intestine cancer laryngeal disease learning disability leiomyoma leukemia liver cancer lung benign neoplasm lung cancer lung carcinoma lymphoblastic lymphoma lymphoid leukemia lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 melanoma microphthalmia mixed glioma mixed-type liposarcoma mongolian spot mucopolysaccharidosis IV multicentric Castleman disease multiple epiphyseal dysplasia myelodysplastic syndrome myeloid leukemia myofibroma myxoid liposarcoma narcolepsy nervous system disease neuroblastoma nonpapillary renal cell carcinoma nutmeg liver obesity obsolete congenital ichthyosiform erythroderma obstructive hydrocephalus optic atrophy osteochondrodysplasia osteomyelitis papillary adenocarcinoma papillary renal cell carcinoma papilloma pathologic nystagmus placenta cancer polydactyly polyhydramnios pseudoxanthoma elasticum ptosis renal carcinoma renal cell carcinoma retinoblastoma rheumatoid arthritis rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 sarcomatoid renal cell carcinoma schizophrenia scoliosis seborrheic keratosis senile degeneration of brain sensorineural hearing loss situs inversus skin disease skin melanoma spondylolisthesis spontaneous ocular nystagmus squamous cell carcinoma squamous cell papilloma steatotic liver disease stomach cancer stomach carcinoma systemic Epstein-Barr virus positive T-cell lymphoma of childhood thyroid gland papillary carcinoma tongue squamous cell carcinoma tracheal calcification tracheal disease tracheal stenosis trilateral retinoblastoma tuberous sclerosis type 2 diabetes mellitus urinary bladder cancer uterine fibroid visual epilepsy
Q8IU81	Interferon regulatory factor 2-binding protein 1	IRF2BP1	Homo sapiens (human)	4	2
Q6N043	Zinc finger protein 280D	ZNF280D KIAA1584 SUHW4 ZNF634	Homo sapiens (human)	3	2
Q6PJT7	Zinc finger CCCH domain-containing protein 14	ZC3H14	Homo sapiens (human)	30	2
P67809	Y-box-binding protein 1	YBX1 NSEP1 YB1	Homo sapiens (human)	8	2
Q9H3H5	UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase	DPAGT1 DPAGT2	Homo sapiens (human)	2	2	Bell's palsy Ebola hemorrhagic fever Lambert-Eaton myasthenic syndrome acute intermittent porphyria agnosia alternating exotropia breast cancer cancer cataract clubfoot colorectal cancer colorectal carcinoma congenital disorder of glycosylation Ij congenital disorder of glycosylation type I congenital disorder of glycosylation congenital myasthenic syndrome 13 congenital myasthenic syndrome congenital nystagmus congenital ptosis cutaneous leishmaniasis developmental and epileptic encephalopathy 36 developmental coordination disorder dissociated nystagmus epilepsy essential hypertension exotropia facial nerve disease facial paralysis familial periodic paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome glycoproteinosis hepatocellular carcinoma hypertension intellectual disability isolated elevated serum creatine phosphokinase levels large intestine cancer learning disability leishmaniasis liver cancer microcephaly monocular exotropia mucolipidosis II alpha/beta myopathy pathologic nystagmus pseudosarcomatous fibromatosis ptosis scoliosis spontaneous ocular nystagmus squamous cell carcinoma stomach cancer stomach carcinoma stuttering syndromic X-linked intellectual disability 94 tongue squamous cell carcinoma tuberculosis visceral leishmaniasis visual epilepsy
Q16186	Proteasomal ubiquitin receptor ADRM1	ADRM1 GP110	Homo sapiens (human)	10	2
P43146	Netrin receptor DCC	DCC IGDCC1	Homo sapiens (human)	6	2
P51003	Poly(A) polymerase alpha	PAPOLA PAP	Homo sapiens (human)	9	2
P55201	Peregrin	BRPF1 BR140	Homo sapiens (human)	1	2
O15021	Microtubule-associated serine/threonine-protein kinase 4	MAST4 KIAA0303	Homo sapiens (human)	1	2
P39023	Large ribosomal subunit protein uL3	RPL3	Homo sapiens (human)	1	2
Q06547	GA-binding protein subunit beta-1	GABPB1 E4TF1B GABPB GABPB2	Homo sapiens (human)	3	2
Q9H061	Transmembrane protein 126A	TMEM126A	Homo sapiens (human)	1	2
P06133	UDP-glucuronosyltransferase 2B4	UGT2B4 UGT2B11	Homo sapiens (human)	1	2	breast cancer cancer cerebral infarction cerebrovascular disease cholestasis embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma hepatocellular carcinoma liver cancer primary biliary cholangitis steatotic liver disease
P23276	Kell blood group glycoprotein	KEL	Homo sapiens (human)	5	2
Q6ZMM2	ADAMTS-like protein 5	ADAMTSL5 THSD6	Homo sapiens (human)	2	2
Q96QV6	Histone H2A type 1-A	H2AC1 H2AFR HIST1H2AA	Homo sapiens (human)	1	2
Q93033	Immunoglobulin superfamily member 2	CD101 EWI101 IGSF2 V7	Homo sapiens (human)	4	2

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