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 **16776 - 16800** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
Q5TB80	Centrosomal protein of 162 kDa	CEP162 C6orf84 KIAA1009 QN1	Homo sapiens (human)	1
Q9HCI5	Melanoma-associated antigen E1	MAGEE1 HCA1 KIAA1587	Homo sapiens (human)	1
Q969M7	NEDD8-conjugating enzyme UBE2F	UBE2F NCE2	Homo sapiens (human)	1
A6NGY5	Olfactory receptor 51F1	OR51F1 OR51F1P	Homo sapiens (human)	1
Q8TD16	Protein bicaudal D homolog 2	BICD2 KIAA0699	Homo sapiens (human)	1
P36639	Oxidized purine nucleoside triphosphate hydrolase	NUDT1 MTH1	Homo sapiens (human)	1
Q9BV86	N-terminal Xaa-Pro-Lys N-methyltransferase 1	NTMT1 C9orf32 METTL11A NRMT NRMT1	Homo sapiens (human)	1
Q96LM1	Putative uncharacterized protein encoded by LINC00615	LINC00615 C12orf37	Homo sapiens (human)	1
Q8N9L1	Zinc finger protein ZIC 4	ZIC4	Homo sapiens (human)	1
Q99618	Cell division cycle-associated protein 3	CDCA3 C8 GRCC8 TOME1	Homo sapiens (human)	1
Q03112	Histone-lysine N-methyltransferase MECOM	MECOM EVI1 MDS1 PRDM3	Homo sapiens (human)	1
Q6UXN9	WD repeat-containing protein 82	WDR82 SWD2 TMEM113 WDR82A	Homo sapiens (human)	1
P84157	Matrix-remodeling-associated protein 7	MXRA7	Homo sapiens (human)	1
Q9NW81	Distal membrane-arm assembly complex protein 2	DMAC2 ATP5SL	Homo sapiens (human)	1
Q15583	Homeobox protein TGIF1	TGIF1 TGIF	Homo sapiens (human)	1
Q9UBV8	Peflin	PEF1 ABP32	Homo sapiens (human)	1
Q9BR11	Zinc finger SWIM domain-containing protein 1	ZSWIM1 C20orf162	Homo sapiens (human)	1
Q15119	[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 2, mitochondrial	PDK2 PDHK2	Homo sapiens (human)	1
Q5JVG2	Zinc finger protein 484	ZNF484	Homo sapiens (human)	1
Q15738	Sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating	NSDHL H105E3	Homo sapiens (human)	1	Bloch-Sulzberger syndrome Joubert syndrome Miller-Dieker lissencephaly syndrome Potter's syndrome Sjogren-Larsson syndrome X-linked chondrodysplasia punctata 1 X-linked chondrodysplasia punctata 2 acquired hyperkeratosis autosomal dominant chondrodysplasia punctata autosomal recessive congenital ichthyosis bilateral renal aplasia chondrodysplasia punctata cleft lip complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cortical dysplasia-focal epilepsy syndrome cutaneous fibrous histiocytoma epidermal nevus epilepsy granuloma annulare head and neck squamous cell carcinoma heart septal defect hidradenoma hydranencephaly hydronephrosis hypertropia hypomelanosis of Ito intellectual disability learning disability lissencephaly mechanical strabismus microcephaly obsolete congenital ichthyosiform erythroderma omphalocele ophthalmoplegia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly skin papilloma skin tag strabismus syndromic X-linked intellectual disability Najm type syringoma umbilical hernia ventricular septal defect verruciform xanthoma of skin visual epilepsy
P69891	Hemoglobin subunit gamma-1	HBG1	Homo sapiens (human)	1
P0CG48	Polyubiquitin-C	UBC	Homo sapiens (human)	1
Q8TCT0	Ceramide kinase	CERK KIAA1646	Homo sapiens (human)	1	Kaposi's sarcoma breast cancer breast carcinoma cancer colitis gastroenteritis ileitis ileocolitis microphthalmia neuroblastoma obesity obsolete Matthew-Wood syndrome schizophrenia 10 schizophrenia
Q5TBC7	Bcl-2-like protein 15	BCL2L15 C1orf178	Homo sapiens (human)	1
P36873	Serine/threonine-protein phosphatase PP1-gamma catalytic subunit	PPP1CC	Homo sapiens (human)	1

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