GlyCosmos Portal

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GlyConnect	April 19, 2023
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The O-GlcNAc Database	June 3, 2024
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Displaying entries **6301 - 6325** of **126547** in total

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UniProt ID ▼	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9UPQ9	Trinucleotide repeat-containing gene 6B protein	TNRC6B KIAA1093	Homo sapiens (human)	9	5
Q9UPQ4	E3 ubiquitin-protein ligase TRIM35	TRIM35 HLS5 KIAA1098	Homo sapiens (human)	1	1
Q9UPQ3	Arf-GAP with GTPase, ANK repeat and PH domain-containing protein 1	AGAP1 CENTG2 KIAA1099	Homo sapiens (human)	0	1
Q9UPQ0	LIM and calponin homology domains-containing protein 1	LIMCH1 KIAA1102	Homo sapiens (human)	10	2
Q9UPP2	IQ motif and SEC7 domain-containing protein 3	IQSEC3 KIAA1110	Homo sapiens (human)	1	1
Q9UPP1	Histone lysine demethylase PHF8	PHF8 KIAA1111 ZNF422	Homo sapiens (human)	5	2
Q9UPN9	E3 ubiquitin-protein ligase TRIM33	TRIM33 KIAA1113 RFG7 TIF1G	Homo sapiens (human)	5	2
Q9UPN7	Serine/threonine-protein phosphatase 6 regulatory subunit 1	PPP6R1 KIAA1115 PP6R1 SAPS1	Homo sapiens (human)	3	1
Q9UPN6	SR-related and CTD-associated factor 8	SCAF8 CCAP7 KIAA1116 RBM16	Homo sapiens (human)	16	3
Q9UPN4	Centrosomal protein of 131 kDa	CEP131 AZI1 KIAA1118	Homo sapiens (human)	2	2
Q9UPN3	Microtubule-actin cross-linking factor 1, isoforms 1/2/3/4/5	MACF1 ABP620 ACF7 KIAA0465 KIAA0754 KIAA1251	Homo sapiens (human)	23	5
Q9UPM6	LIM/homeobox protein Lhx6	LHX6 LHX6.1	Homo sapiens (human)	0	1
Q9UPC5	Probable G-protein coupled receptor 34	GPR34	Homo sapiens (human)	5	0
Q9UPA5	Protein bassoon	BSN KIAA0434 ZNF231	Homo sapiens (human)	80	1
Q9UP95	Solute carrier family 12 member 4	SLC12A4 KCC1	Homo sapiens (human)	5	7
Q9UP83	Conserved oligomeric Golgi complex subunit 5	COG5 GOLTC1 GTC90	Homo sapiens (human)	1	2	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Cauda equina syndrome Friedreich ataxia Laron syndrome Pick's disease Reye syndrome achondroplasia agnosia arthritis arthropathy atrial fibrillation cerebral degeneration congenital disorder of glycosylation type II congenital disorder of glycosylation type IIi congenital disorder of glycosylation coronary artery disease cryptorchidism developmental coordination disorder epilepsy hypertropia intellectual disability learning disability leiomyoma mechanical strabismus microcephaly myofibroma neurogenic bladder oligohydramnios ophthalmoplegia osteoarthritis placental insufficiency sensorineural hearing loss strabismus syndromic X-linked intellectual disability 94 uterine fibroid visual epilepsy
Q9UP79	A disintegrin and metalloproteinase with thrombospondin motifs 8	ADAMTS8 METH2	Homo sapiens (human)	6	1
Q9UP52	Transferrin receptor protein 2	TFR2	Homo sapiens (human)	4	0
Q9UP38	Frizzled-1	FZD1	Homo sapiens (human)	4	3
Q9UNZ5	Leydig cell tumor 10 kDa protein homolog	C19orf53	Homo sapiens (human)	0	1
Q9UNZ2	NSFL1 cofactor p47	NSFL1C UBXN2C	Homo sapiens (human)	0	1
Q9UNY4	Transcription termination factor 2	TTF2	Homo sapiens (human)	1	2
Q9UNX4	WD repeat-containing protein 3	WDR3	Homo sapiens (human)	2	1
Q9UNX3	Ribosomal protein uL24-like	RPL26L1 RPL26P1	Homo sapiens (human)	0	1
Q9UNW9	RNA-binding protein Nova-2	NOVA2 ANOVA NOVA3	Homo sapiens (human)	0	1

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