GlyCosmos Portal

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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 **118651 - 118675** 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
Q9P055	JNK1/MAPK8-associated membrane protein	JKAMP C14orf100 JAMP	Homo sapiens (human)	2	1
Q9P0J1	[Pyruvate dehydrogenase [acetyl-transferring]]-phosphatase 1, mitochondrial	PDP1 PDP PPM2C	Homo sapiens (human)	1	1
Q9P0J7	E3 ubiquitin-protein ligase KCMF1	KCMF1 FIGC ZZZ1	Homo sapiens (human)	2	2
Q9P0K1	Disintegrin and metalloproteinase domain-containing protein 22	ADAM22 MDC2	Homo sapiens (human)	5	9
Q9P0K7	Ankycorbin	RAI14 KIAA1334 NORPEG	Homo sapiens (human)	5	4
Q9P0K8	Forkhead box protein J2	FOXJ2 FHX	Homo sapiens (human)	3	1
Q9P0L0	Vesicle-associated membrane protein-associated protein A	VAPA VAP33	Homo sapiens (human)	4	2
Q9P0L9	Polycystin-2-like protein 1	PKD2L1 PKD2L PKDL TRPP3	Homo sapiens (human)	4	0
Q9P0M2	A-kinase anchor protein 7 isoform gamma	AKAP7 AKAP18	Homo sapiens (human)	2	1
Q9P0M6	Core histone macro-H2A.2	MACROH2A2 H2AFY2	Homo sapiens (human)	1	1
Q9P0M9	Large ribosomal subunit protein bL27m	MRPL27	Homo sapiens (human)	0	1
Q9P0S9	Transmembrane protein 14C	TMEM14C C6orf53	Homo sapiens (human)	0	1
Q9P0T7	Proton-transporting V-type ATPase complex assembly regulator TMEM9	TMEM9 DERP4 TMEM9A	Homo sapiens (human)	6	4
Q9P0V8	SLAM family member 8	SLAMF8 BLAME	Homo sapiens (human)	1	1
Q9P0V9	Septin-10	SEPTIN10 SEPT10	Homo sapiens (human)	0	1
Q9P0W2	SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily E member 1-related	HMG20B BRAF35 HMGX2 HMGXB2 SMARCE1R	Homo sapiens (human)	0	1
Q9P0X4	Voltage-dependent T-type calcium channel subunit alpha-1I	CACNA1I KIAA1120	Homo sapiens (human)	7	1
Q9P109	Beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 4	GCNT4	Homo sapiens (human)	2	0
Q9P121	Neurotrimin	NTM IGLON2 NT	Homo sapiens (human)	7	0	Kartagener syndrome Mycobacterium avium complex disease Parkinson's disease acquired immunodeficiency syndrome actinic keratosis acute myeloid leukemia acute myocardial infarction attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bronchiectasis cancer chronic obstructive pulmonary disease congenital aphakia congenital heart disease congestive heart failure coronary thrombosis depressive disorder embryoma endophthalmitis esophagitis familial medullary thyroid carcinoma gallbladder disease gastroesophageal reflux disease hepatocellular carcinoma intracranial aneurysm late onset Parkinson's disease leprosy liver cancer liver disease lung disease lymphadenitis major depressive disorder melancholic depression multiple endocrine neoplasia type 2A myocardial infarction myopia neurotic disorder nicotine dependence obsolete melancholia peptic esophagitis primary ciliary dyskinesia 1 primary ciliary dyskinesia primary open angle glaucoma pulmonary tuberculosis schizophrenia seborrheic keratosis silent myocardial infarction skin disease thyroid gland medullary carcinoma tuberculosis tuberculous pneumothorax
Q9P126	C-type lectin domain family 1 member B	CLEC1B CLEC2	Homo sapiens (human)	3	1	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 Evans' syndrome Marfan syndrome Pick's disease Reye syndrome adult respiratory distress syndrome androgen insensitivity syndrome arteriosclerotic cardiovascular disease atherosclerosis atrioventricular septal defect autoimmune thrombocytopenic purpura bacterial sepsis blood coagulation disease cancer cerebral degeneration cerebral infarction cerebrovascular disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma coronary artery disease diabetes mellitus diabetic ketoacidosis embryoma gallbladder disease hematopoietic system disease hemolytic-uremic syndrome hepatocellular carcinoma liver cancer liver disease lung benign neoplasm melanoma newborn respiratory distress syndrome nonpapillary renal cell carcinoma nutmeg liver obsolete inherited blood coagulation disease papillary renal cell carcinoma pneumonia renal carcinoma renal cell carcinoma rheumatoid arthritis sarcomatoid renal cell carcinoma situs inversus skin melanoma split hand-foot malformation 1 stomach cancer stomach carcinoma thrombocytopenia due to platelet alloimmunization thrombocytopenia thrombophilia thrombotic thrombocytopenic purpura tuberous sclerosis type 2 diabetes mellitus viral infectious disease
Q9P1A6	Disks large-associated protein 2	DLGAP2 C8orf68 DAP2 ERICH1-AS1	Homo sapiens (human)	3	3
Q9P1D8	Putative uncharacterized protein PRO2289	PRO2289	Homo sapiens (human)	2	1
Q9P1P4	Putative trace amine-associated receptor 3	TAAR3P GPR57 TAAR3	Homo sapiens (human)	1	0
Q9P1P5	Trace amine-associated receptor 2	TAAR2 GPR58	Homo sapiens (human)	3	0
Q9P1Q0	Vacuolar protein sorting-associated protein 54	VPS54 HCC8	Homo sapiens (human)	0	1

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