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 **1526 - 1550** 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
D5FHV8	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9ULX9	Transcription factor MafF	MAFF	Homo sapiens (human)	0	1
Q7L5L3	Lysophospholipase D GDPD3	GDPD3 GDE7	Homo sapiens (human)	0	1	Fabry disease Wolman disease chylomicron retention disease lipid storage disease
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
H0YCY8	Dipeptidyl peptidase 1	CTSC	Homo sapiens (human)	1	0
Q9Y2T2	AP-3 complex subunit mu-1	AP3M1	Homo sapiens (human)	0	1
Q9UN71	Protocadherin gamma-B4	PCDHGB4 CDH20 FIB2	Homo sapiens (human)	2	4
A0A0K0KRE0	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q14324	Myosin-binding protein C, fast-type	MYBPC2 MYBPCF	Homo sapiens (human)	0	1
P61011	Signal recognition particle subunit SRP54	SRP54	Homo sapiens (human)	3	3
Q01726	Melanocyte-stimulating hormone receptor	MC1R MSHR	Homo sapiens (human)	1	1
A0A140T9H5	HLA class I histocompatibility antigen, C alpha chain	HLA-C	Homo sapiens (human)	1	0
Q15654	Thyroid receptor-interacting protein 6	TRIP6 OIP1	Homo sapiens (human)	3	1
Q9UHI8	A disintegrin and metalloproteinase with thrombospondin motifs 1	ADAMTS1 KIAA1346 METH1	Homo sapiens (human)	10	3
Q8IU81	Interferon regulatory factor 2-binding protein 1	IRF2BP1	Homo sapiens (human)	4	2
A1KQR2	MHC class I antigen (Fragment)	HLA-Cw	Homo sapiens (human)	1	0
A0A068W6H0	Basal cell adhesion molecule (Lutheran blood group)	BCAM	Homo sapiens (human)	3	0
G1ENT0	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q6P2E9	Enhancer of mRNA-decapping protein 4	EDC4 HEDLS	Homo sapiens (human)	0	1
Q9UBJ2	ATP-binding cassette sub-family D member 2	ABCD2 ALD1 ALDL1 ALDR ALDRP	Homo sapiens (human)	2	0
P11274	Breakpoint cluster region protein	BCR BCR1 D22S11	Homo sapiens (human)	1	1
Q9HAV7	GrpE protein homolog 1, mitochondrial	GRPEL1 GREPEL1	Homo sapiens (human)	0	1
Q12841	Follistatin-related protein 1	FSTL1 FRP	Homo sapiens (human)	8	27
M9P9A7	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q8N7A1	Kelch domain-containing protein 1	KLHDC1	Homo sapiens (human)	0	1

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