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 **4126 - 4150** 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
Q8NCW6	Polypeptide N-acetylgalactosaminyltransferase 11	GALNT11	Homo sapiens (human)	2	5	Richter's syndrome cancer chronic lymphocytic leukemia colorectal cancer colorectal carcinoma embryoma idiopathic scoliosis large intestine cancer
I1W1M7	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9BYT8	Neurolysin, mitochondrial	NLN AGTBP KIAA1226	Homo sapiens (human)	0	1
A0A6H2U4B7	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
Q5T985	Inter-alpha-trypsin inhibitor heavy chain 2	ITIH2	Homo sapiens (human)	1	0
I2B2X6	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q8IZT6	Abnormal spindle-like microcephaly-associated protein	ASPM MCPH5	Homo sapiens (human)	3	1
Q6PGQ1	Aspartate-rich protein 1	DRICH1 C22orf43	Homo sapiens (human)	0	1
Q8IZE3	Protein-associating with the carboxyl-terminal domain of ezrin	SCYL3 PACE1	Homo sapiens (human)	0	1
Q7Z3S7	Voltage-dependent calcium channel subunit alpha-2/delta-4	CACNA2D4	Homo sapiens (human)	3	1	achromatopsia acquired color blindness acquired immunodeficiency syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness blue color blindness borderline personality disorder color blindness cone dystrophy cone-rod dystrophy 2 cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness disease of mental health dissociated nystagmus eye disease human immunodeficiency virus infectious disease hypertropia intermittent explosive disorder mechanical strabismus night blindness obsolete asthenopia ophthalmoplegia pathologic nystagmus psychotic disorder red color blindness red-green color blindness spontaneous ocular nystagmus strabismus
A0A7I2V3M6	Cathepsin C	CTSC	Homo sapiens (human)	1	0
Q9NVC6	Mediator of RNA polymerase II transcription subunit 17	MED17 ARC77 CRSP6 DRIP77 DRIP80 TRAP80	Homo sapiens (human)	0	1
Q93074	Mediator of RNA polymerase II transcription subunit 12	MED12 ARC240 CAGH45 HOPA KIAA0192 TNRC11 TRAP230	Homo sapiens (human)	0	1
G1EQA8	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q8N307	Mucin-20	MUC20 KIAA1359	Homo sapiens (human)	14	2
I6SJ89	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q8N393	Zinc finger protein 786	ZNF786	Homo sapiens (human)	0	1
A0A3S6RFZ7	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
K7P5G0	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q7Z5J4	Retinoic acid-induced protein 1	RAI1 KIAA1820	Homo sapiens (human)	6	1
Q96EV2	RNA-binding protein 33	RBM33 PRR8	Homo sapiens (human)	8	2
Q6NYC1	Bifunctional arginine demethylase and lysyl-hydroxylase JMJD6	JMJD6 KIAA0585 PSR PTDSR	Homo sapiens (human)	0	1
Q16676	Forkhead box protein D1	FOXD1 FKHL8 FREAC4	Homo sapiens (human)	2	1
P11908	Ribose-phosphate pyrophosphokinase 2	PRPS2	Homo sapiens (human)	1	1	Sertoli cell-only syndrome X-linked spermatogenic failure 1 Y-linked spermatogenic failure 1 cancer embryoma oligospermia systemic lupus erythematosus
P11678	Eosinophil peroxidase	EPX EPER EPO EPP	Homo sapiens (human)	6	4

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