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 **13826 - 13850** 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
P21781	Fibroblast growth factor 7	FGF7 KGF	Homo sapiens (human)	2	1
Q6ZS02	Putative GED domain-containing protein DNM1P46	DNM1P46 C15orf51	Homo sapiens (human)	2	1
Q96NY8	Nectin-4	NECTIN4 LNIR PRR4 PVRL4	Homo sapiens (human)	2	7
A0A0S2Z455	Serpin peptidase inhibitor clade I member 1 isoform 1 (Fragment)	SERPINI1	Homo sapiens (human)	2	0
P01859	Immunoglobulin heavy constant gamma 2	IGHG2	Homo sapiens (human)	2	157
Q99788	Chemerin-like receptor 1	CMKLR1 CHEMR23 DEZ	Homo sapiens (human)	2	0
Q96P65	Pyroglutamylated RF-amide peptide receptor	QRFPR GPR103	Homo sapiens (human)	2	1
Q08J23	RNA cytosine C(5)-methyltransferase NSUN2	NSUN2 SAKI TRM4	Homo sapiens (human)	2	3
Q13310	Polyadenylate-binding protein 4	PABPC4 APP1 PABP4	Homo sapiens (human)	2	1
O75970	Multiple PDZ domain protein	MPDZ MUPP1	Homo sapiens (human)	2	5
P21452	Substance-K receptor	TACR2 NK2R NKNAR TAC2R	Homo sapiens (human)	2	0
A6NE01	Protein FAM186A	FAM186A	Homo sapiens (human)	2	1
Q96S15	GATOR2 complex protein WDR24	WDR24 C16orf21	Homo sapiens (human)	2	2
O75914	Serine/threonine-protein kinase PAK 3	PAK3 OPHN3	Homo sapiens (human)	2	0
P19526	Galactoside alpha-(1,2)-fucosyltransferase 1	FUT1 H HSC	Homo sapiens (human)	2	0	B-cell lymphoma Edwards syndrome Fanconi anemia complementation group A Fanconi anemia complementation group D2 Fanconi anemia Kawasaki disease MHC class II deficiency Scheie syndrome T-cell acute lymphoblastic leukemia Wiskott-Aldrich syndrome X-linked lymphoproliferative syndrome 1 X-linked lymphoproliferative syndrome 2 X-linked severe combined immunodeficiency acquired immunodeficiency syndrome acquired polycythemia acute myeloid leukemia acute promyelocytic leukemia adenosine deaminase deficiency adrenoleukodystrophy alcoholic hepatitis alcoholic liver cirrhosis anemia arthritis arthropathy autoimmune disease autoimmune lymphoproliferative syndrome azoospermia beta thalassemia bile duct adenocarcinoma bile duct carcinoma bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma catecholaminergic polymorphic ventricular tachycardia 1 catecholaminergic polymorphic ventricular tachycardia 2 catecholaminergic polymorphic ventricular tachycardia 3 catecholaminergic polymorphic ventricular tachycardia 4 catecholaminergic polymorphic ventricular tachycardia 5 catecholaminergic polymorphic ventricular tachycardia cerebral infarction cerebrovascular disease childhood leukemia cholangiocarcinoma chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma combined T cell and B cell immunodeficiency congenital hemolytic anemia cutaneous porphyria cystic fibrosis diarrhea distal arthrogryposis embryoma erythropoietic protoporphyria erythropoietin polycythemia essential thrombocythemia factor VIII deficiency familial erythrocytosis 2 gallbladder disease glycogen storage disease II head and neck squamous cell carcinoma hematologic cancer hematopoietic system disease hemochromatosis type 1 hemochromatosis hemoglobin C disease hemoglobin D disease hemoglobin E disease hemoglobinopathy hemophagocytic lymphohistiocytosis hepatitis C hepatocellular carcinoma human immunodeficiency virus infectious disease immune system disease inherited metabolic disorder intrahepatic cholangiocarcinoma juvenile myelomonocytic leukemia large intestine cancer leukemia liver cancer liver cirrhosis liver disease lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung squamous cell carcinoma lysosomal storage disease macrocytic anemia malignant teratoma mantle cell lymphoma mature teratoma melanoma metachromatic leukodystrophy mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis multiple myeloma myelodysplastic syndrome myeloproliferative neoplasm obsolete ymphosarcoma orofaciodigital syndrome VIII osteoarthritis ovarian cancer ovarian carcinoma pancytopenia paroxysmal nocturnal hemoglobinuria polycythemia vera polycythemia progressive muscular atrophy prostate cancer prostate carcinoma proteinuria psoriatic arthritis sarcomatoid carcinoma severe combined immunodeficiency sickle cell anemia skin benign neoplasm skin cancer skin melanoma skin squamous cell carcinoma spinal muscular atrophy squamous cell carcinoma stomach cancer stomach carcinoma stress polycythemia teratocarcinoma teratoma tongue squamous cell carcinoma
Q9NSP4	Centromere protein M	CENPM C22orf18 ICEN39 PANE1	Homo sapiens (human)	2	1
A0A1W2PPN1	MHC class I polypeptide-related sequence A	MICA	Homo sapiens (human)	2	0
O94812	BAI1-associated protein 3	BAIAP3 KIAA0734	Homo sapiens (human)	2	1
Q9P2F8	Signal-induced proliferation-associated 1-like protein 2	SIPA1L2 KIAA1389	Homo sapiens (human)	2	2
O60308	Centrosomal protein of 104 kDa	CEP104 KIAA0562	Homo sapiens (human)	2	1
Q6UX04	Spliceosome-associated protein CWC27 homolog	CWC27 SDCCAG10	Homo sapiens (human)	2	1
Q96DX4	RING finger and SPRY domain-containing protein 1	RSPRY1 KIAA1972	Homo sapiens (human)	2	2
P35414	Apelin receptor	APLNR AGTRL1 APJ	Homo sapiens (human)	2	0
Q86WS5	Transmembrane protease serine 12	TMPRSS12	Homo sapiens (human)	2	0
E7EMM4	Acid ceramidase	ASAH1	Homo sapiens (human)	2	0

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