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 **15051 - 15075** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of GlyTouCan IDs	Disease Ontology
Q9NRW1	Ras-related protein Rab-6B	RAB6B	Homo sapiens (human)	1
Q8N196	Homeobox protein SIX5	SIX5 DMAHP	Homo sapiens (human)	1
O43808	Peroxisomal membrane protein PMP34	SLC25A17 PMP34	Homo sapiens (human)	1
Q2KHM9	Protein moonraker	KIAA0753 MNR OFIP	Homo sapiens (human)	1
Q9BTP7	Fanconi anemia core complex-associated protein 24	FAAP24 C19orf40	Homo sapiens (human)	1
Q8IVF5	Rho guanine nucleotide exchange factor TIAM2	TIAM2 KIAA2016 STEF	Homo sapiens (human)	1
Q6ZN17	Protein lin-28 homolog B	LIN28B CSDD2	Homo sapiens (human)	1
Q9UBQ5	Eukaryotic translation initiation factor 3 subunit K	EIF3K EIF3S12	Homo sapiens (human)	1
Q96JJ6	Junctophilin-4	JPH4 JPHL1 KIAA1831	Homo sapiens (human)	1
Q9H0K1	Serine/threonine-protein kinase SIK2	SIK2 KIAA0781 QIK SNF1LK2	Homo sapiens (human)	1
Q13162	Peroxiredoxin-4	PRDX4	Homo sapiens (human)	1
Q66PJ3	ADP-ribosylation factor-like protein 6-interacting protein 4	ARL6IP4	Homo sapiens (human)	1
Q8NBR9	Uncharacterized protein NDUFV1-DT	NDUFV1-DT C11orf72	Homo sapiens (human)	1
A4D1E1	Zinc finger protein 804B	ZNF804B	Homo sapiens (human)	1
Q9BT22	Chitobiosyldiphosphodolichol beta-mannosyltransferase	ALG1 HMAT1 HMT1	Homo sapiens (human)	1	B-cell lymphoma Cauda equina syndrome Creutzfeldt-Jakob disease Graves' disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Walker-Warburg syndrome amyotrophic lateral sclerosis type 1 breast cancer breast carcinoma breast fibroadenoma bronchus cancer bronchus carcinoma cancer cardiomyopathy cerebral degeneration cerebral infarction cerebrovascular disease colon cancer colonic benign neoplasm congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation congenital muscular dystrophy-dystroglycanopathy type A1 diabetes mellitus endomyocardial fibrosis enophthalmos epilepsy familial hypertrophic cardiomyopathy familial nephrotic syndrome focal epilepsy glomerulonephritis goiter hepatocellular carcinoma hyperthyroidism hypertrophic cardiomyopathy hypogonadism kidney disease laryngeal benign neoplasm laryngeal carcinoma laryngeal squamous cell carcinoma larynx cancer liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lupus nephritis lymphoma malignant pleural mesothelioma microcephaly nephritis nephrosis nephrotic syndrome type 1 nephrotic syndrome neurogenic bladder nodular goiter obsolete exophthalmos obsolete ymphosarcoma orbital disease partial motor epilepsy placental insufficiency pyoureter reticulosarcoma schizophrenia scoliosis systemic lupus erythematosus thyroid gland disease thyrotoxicosis type 2 diabetes mellitus urinary tract obstruction visual epilepsy
Q93062	RNA-binding protein with multiple splicing	RBPMS HERMES	Homo sapiens (human)	1
Q13401	Putative postmeiotic segregation increased 2-like protein 3	PMS2P3 PMS2L3 PMS2L9 PMS5 PMSR3	Homo sapiens (human)	1
Q4G0X4	BTB/POZ domain-containing protein KCTD21	KCTD21	Homo sapiens (human)	1
Q9Y2T1	Axin-2	AXIN2	Homo sapiens (human)	1
Q5VTL8	Pre-mRNA-splicing factor 38B	PRPF38B	Homo sapiens (human)	1
Q9NVV2	Putative uncharacterized protein C19orf73	C19orf73	Homo sapiens (human)	1
Q8N1F8	Serine/threonine-protein kinase 11-interacting protein	STK11IP KIAA1898 LIP1 LKB1IP STK11IP1	Homo sapiens (human)	1
V9HVZ7	Actin, cytoplasmic 2	HEL-176	Homo sapiens (human)	1
A4D1E9	GTP-binding protein 10	GTPBP10 OBGH2	Homo sapiens (human)	1
O94788	Retinal dehydrogenase 2	ALDH1A2 RALDH2	Homo sapiens (human)	1

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