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 **3876 - 3900** of **18496** in total

« First

‹ Prev

…

152

153

154

155

156

157

158

159

160

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
P78413	Iroquois-class homeodomain protein IRX-4	IRX4 IRXA3	Homo sapiens (human)	0	1
Q6YHU6	tRNA (32-2'-O)-methyltransferase regulator THADA	THADA GITA KIAA1767	Homo sapiens (human)	1	1
Q969S3	Cytoplasmic 60S subunit biogenesis factor ZNF622	ZNF622 ZPR9	Homo sapiens (human)	0	1
Q96MN5	Transcription elongation factor A N-terminal and central domain-containing protein 2	TCEANC2 C1orf83	Homo sapiens (human)	0	1
Q96AY4	Tetratricopeptide repeat protein 28	TTC28 KIAA1043 TPRBK	Homo sapiens (human)	5	1
Q9Y2L6	FERM domain-containing protein 4B	FRMD4B GRSP1 KIAA1013	Homo sapiens (human)	0	1
Q92551	Inositol hexakisphosphate kinase 1	IP6K1 IHPK1 KIAA0263	Homo sapiens (human)	0	1
Q5VV42	Threonylcarbamoyladenosine tRNA methylthiotransferase	CDKAL1	Homo sapiens (human)	1	1
Q9P2W1	Homologous-pairing protein 2 homolog	PSMC3IP HOP2 TBPIP	Homo sapiens (human)	0	1
O15440	ATP-binding cassette sub-family C member 5	ABCC5 MRP5	Homo sapiens (human)	9	1
Q3B820	Protein FAM161A	FAM161A	Homo sapiens (human)	0	1
Q9Y493	Zonadhesin	ZAN	Homo sapiens (human)	11	1
P35908	Keratin, type II cytoskeletal 2 epidermal	KRT2 KRT2A KRT2E	Homo sapiens (human)	3	1
Q08554	Desmocollin-1	DSC1 CDHF1	Homo sapiens (human)	8	1
Q9NUQ9	CYFIP-related Rac1 interactor B	CYRIB CYRI FAM49B	Homo sapiens (human)	0	1
O95295	SNARE-associated protein Snapin	SNAPIN BLOC1S7 SNAP25BP SNAPAP	Homo sapiens (human)	0	1
Q9GZT9	Egl nine homolog 1	EGLN1 C1orf12	Homo sapiens (human)	0	1
Q9UBC5	Unconventional myosin-Ia	MYO1A MYHL	Homo sapiens (human)	1	1
P32119	Peroxiredoxin-2	PRDX2 NKEFB TDPX1	Homo sapiens (human)	5	1
O14607	Histone demethylase UTY	UTY KDM6C	Homo sapiens (human)	1	1
P78382	CMP-sialic acid transporter	SLC35A1	Homo sapiens (human)	0	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 Behcet's disease Marfan syndrome Papillon-Lefevre disease Pick's disease Reye syndrome acute myocardial infarction agranulocytosis amyotrophic lateral sclerosis anhidrosis anterior horn cell disease aortic valve insufficiency arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis brain disease brain stem infarction cancer cardiovascular system disease cellulitis central nervous system cancer cerebral artery occlusion cerebral degeneration cerebral infarction cerebrovascular disease cone-rod dystrophy 2 cone-rod dystrophy congenital disorder of glycosylation Iq congenital disorder of glycosylation type II congenital disorder of glycosylation type IIf congenital disorder of glycosylation congenital nystagmus congestive heart failure coronary artery disease coronary thrombosis diabetes mellitus diabetic ketoacidosis diabetic macular edema dissociated nystagmus embryoma epilepsy episodic kinesigenic dyskinesia 1 essential hypertension gliosarcoma glucose intolerance heart disease hepatitis B hepatocellular carcinoma high grade glioma hyperglycemia hypertension hypohidrosis immune system disease inflammatory bowel disease 1 inflammatory bowel disease influenza intellectual disability lateral sclerosis learning disability lingual-facial-buccal dyskinesia liver cancer microcephaly mixed glioma motor neuron disease myocardial infarction myotonic dystrophy type 2 neutropenia obesity obsolete type 1 diabetes mellitus 9 osteoarthritis pathologic nystagmus placental insufficiency pneumonia prediabetes syndrome progressive bulbar palsy progressive muscular atrophy proteinuria severe congenital neutropenia silent myocardial infarction situs inversus spontaneous ocular nystagmus substance abuse substance-related disorder thrombocytopenia tuberous sclerosis type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis viral infectious disease visual epilepsy
Q16637	Survival motor neuron protein	SMN1 SMN2 SMN SMNC SMNT	Homo sapiens (human)	0	1
Q15651	High mobility group nucleosome-binding domain-containing protein 3	HMGN3 TRIP7	Homo sapiens (human)	0	1
Q8N3T6	Transmembrane protein 132C	TMEM132C	Homo sapiens (human)	3	1
O95600	Krueppel-like factor 8	KLF8 BKLF3 ZNF741	Homo sapiens (human)	0	1

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements