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 **14926 - 14950** 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
Q9NTX5	Ethylmalonyl-CoA decarboxylase	ECHDC1	Homo sapiens (human)	1	1	bladder carcinoma breast cancer breast carcinoma melanoma ovarian cancer ovarian carcinoma skin melanoma urinary bladder cancer
Q13011	Delta(3,5)-Delta(2,4)-dienoyl-CoA isomerase, mitochondrial	ECH1	Homo sapiens (human)	1	1
O95672	Endothelin-converting enzyme-like 1	ECEL1 XCE	Homo sapiens (human)	3	0
P0DPD6	Endothelin-converting enzyme 2	ECE2 KIAA0604	Homo sapiens (human)	9	1
P42892	Endothelin-converting enzyme 1	ECE1	Homo sapiens (human)	16	50
B4DKB2	Endothelin-converting enzyme 1	ECE1	Homo sapiens (human)	3	0
E9PJG1	Endothelin-converting enzyme 1 (Fragment)	ECE1	Homo sapiens (human)	1	0
A0A3B3ISF9	Endothelin-converting enzyme 1	ECE1	Homo sapiens (human)	3	0
O95905	Protein ecdysoneless homolog	ECD	Homo sapiens (human)	0	1
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
Q99848	Probable rRNA-processing protein EBP2	EBNA1BP2 EBP2	Homo sapiens (human)	0	1
Q14213	Interleukin-27 subunit beta	EBI3 IL27B	Homo sapiens (human)	2	0
Q9BQW3	Transcription factor COE4	EBF4 COE4 KIAA1442	Homo sapiens (human)	0	1
Q96JC9	ELL-associated factor 1	EAF1	Homo sapiens (human)	1	1
A0AVK6	Transcription factor E2F8	E2F8	Homo sapiens (human)	2	1
Q96AV8	Transcription factor E2F7	E2F7	Homo sapiens (human)	1	1
O75461	Transcription factor E2F6	E2F6	Homo sapiens (human)	0	1
Q16254	Transcription factor E2F4	E2F4	Homo sapiens (human)	0	1
Q14209	Transcription factor E2F2	E2F2	Homo sapiens (human)	1	1
Q01094	Transcription factor E2F1	E2F1 RBBP3	Homo sapiens (human)	1	1
Q86YF9	Cilium assembly protein DZIP1	DZIP1 DZIP DZIP2 KIAA0996	Homo sapiens (human)	1	1
Q9NVP4	Double zinc ribbon and ankyrin repeat-containing protein 1	DZANK1 C20orf12 C20orf84	Homo sapiens (human)	0	1
O75923	Dysferlin	DYSF FER1L1	Homo sapiens (human)	0	1
Q9NR20	Dual specificity tyrosine-phosphorylation-regulated kinase 4	DYRK4	Homo sapiens (human)	0	1
Q92630	Dual specificity tyrosine-phosphorylation-regulated kinase 2	DYRK2	Homo sapiens (human)	0	1

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