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 **2801 - 2825** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
V9HW77	Creatine kinase B-type	HEL-211	Homo sapiens (human)	1
Q9NRG4	N-lysine methyltransferase SMYD2	SMYD2 KMT3C	Homo sapiens (human)	1
Q9Y399	Small ribosomal subunit protein uS2m	MRPS2	Homo sapiens (human)	1
Q9H1Y0	Autophagy protein 5	ATG5 APG5L ASP	Homo sapiens (human)	1
Q99933	BAG family molecular chaperone regulator 1	BAG1 HAP	Homo sapiens (human)	1
P17174	Aspartate aminotransferase, cytoplasmic	GOT1	Homo sapiens (human)	1
Q5JS13	Ras-specific guanine nucleotide-releasing factor RalGPS1	RALGPS1 KIAA0351 RALGEF2	Homo sapiens (human)	1
P78386	Keratin, type II cuticular Hb5	KRT85 KRTHB5	Homo sapiens (human)	1
P22102	Trifunctional purine biosynthetic protein adenosine-3	GART PGFT PRGS	Homo sapiens (human)	1
Q96LR5	Ubiquitin-conjugating enzyme E2 E2	UBE2E2 UBCH8	Homo sapiens (human)	1
P46777	Large ribosomal subunit protein uL18	RPL5	Homo sapiens (human)	1
Q9BZF1	Oxysterol-binding protein-related protein 8	OSBPL8 KIAA1451 ORP8 OSBP10	Homo sapiens (human)	1
O00479	High mobility group nucleosome-binding domain-containing protein 4	HMGN4 HMG17L3 NHC	Homo sapiens (human)	1
P62070	Ras-related protein R-Ras2	RRAS2 TC21	Homo sapiens (human)	1
A6NFN9	Protein ANKUB1	ANKUB1 C3orf16	Homo sapiens (human)	1
Q5JV73	FERM and PDZ domain-containing protein 3	FRMPD3 KIAA1817	Homo sapiens (human)	1
Q6NUP7	Serine/threonine-protein phosphatase 4 regulatory subunit 4	PPP4R4 KIAA1622 PP4R4	Homo sapiens (human)	1
O00311	Cell division cycle 7-related protein kinase	CDC7 CDC7L1	Homo sapiens (human)	1
Q8NA70	Protein FAM47B	FAM47B	Homo sapiens (human)	1
Q13435	Splicing factor 3B subunit 2	SF3B2 SAP145	Homo sapiens (human)	1
Q9NP73	UDP-N-acetylglucosamine transferase subunit ALG13	ALG13 CXorf45 GLT28D1	Homo sapiens (human)	1	Bell's palsy Meckel's diverticulum West syndrome agnosia attention deficit hyperactivity disorder autistic disorder blindness cerebral degeneration choreatic disease clubfoot congenital disorder of glycosylation type I congenital disorder of glycosylation congenital nystagmus craniosynostosis developmental and epileptic encephalopathy 36 dissociated nystagmus epilepsy facial nerve disease facial paralysis focal segmental glomerulosclerosis hypophosphatemia intellectual disability learning disability lung cancer lung non-small cell carcinoma microcephaly non-syndromic X-linked intellectual disability obesity obsolete infantile epileptic encephalopathy optic atrophy pathologic nystagmus placental insufficiency pyloric stenosis spontaneous ocular nystagmus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 visual epilepsy
Q14210	Lymphocyte antigen 6D	LY6D E48	Homo sapiens (human)	1
Q8N5J2	Ubiquitin carboxyl-terminal hydrolase MINDY-1	MINDY1 FAM63A KIAA1390	Homo sapiens (human)	1
Q9BTM1	Histone H2A.J	H2AJ H2AFJ	Homo sapiens (human)	1
G3V0H7	Putative solute carrier organic anion transporter family member 1B7	SLCO1B7 LST3 LST3TM12	Homo sapiens (human)	1

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