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 **16901 - 16925** 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
A0A078BFK3	Transforming growth factor, beta 1 (Fragment)	TGFB1	Homo sapiens (human)	1	0
A0A078BCJ0	Transforming growth factor, beta 1 (Fragment)	TGFB1	Homo sapiens (human)	1	0
A0A078BCH8	Transforming growth factor, beta 1 (Fragment)	TGFB1	Homo sapiens (human)	1	0
W8DYQ2	Transforming growth factor, beta receptor II delta	TGFBR2	Homo sapiens (human)	1	0
W8DXL6	Transforming growth factor, beta receptor II gamma	TGFBR2	Homo sapiens (human)	1	0
Q15582	Transforming growth factor-beta-induced protein ig-h3	TGFBI BIGH3	Homo sapiens (human)	2	1
P61586	Transforming protein RhoA	RHOA ARH12 ARHA RHO12	Homo sapiens (human)	2	1
Q01995	Transgelin	TAGLN SM22 WS3-10	Homo sapiens (human)	4	1
P37802	Transgelin-2	TAGLN2 KIAA0120	Homo sapiens (human)	7	3
O75762	Transient receptor potential cation channel subfamily A member 1	TRPA1 ANKTM1	Homo sapiens (human)	2	0
Q7Z4N2	Transient receptor potential cation channel subfamily M member 1	TRPM1 LTRPC1 MLSN MLSN1	Homo sapiens (human)	1	0
Q9HCF6	Transient receptor potential cation channel subfamily M member 3	TRPM3 KIAA1616 LTRPC3	Homo sapiens (human)	2	2
Q8TD43	Transient receptor potential cation channel subfamily M member 4	TRPM4 LTRPC4	Homo sapiens (human)	1	0
Q9BX84	Transient receptor potential cation channel subfamily M member 6	TRPM6 CHAK2	Homo sapiens (human)	1	1
Q7Z2W7	Transient receptor potential cation channel subfamily M member 8	TRPM8 LTRPC6 TRPP8	Homo sapiens (human)	1	1
Q8NER1	Transient receptor potential cation channel subfamily V member 1	TRPV1 VR1	Homo sapiens (human)	1	0
Q9Y5S1	Transient receptor potential cation channel subfamily V member 2	TRPV2 VRL	Homo sapiens (human)	1	0
Q9NQA5	Transient receptor potential cation channel subfamily V member 5	TRPV5 ECAC1	Homo sapiens (human)	1	0
Q9H1D0	Transient receptor potential cation channel subfamily V member 6	TRPV6 ECAC2	Homo sapiens (human)	4	1
P55072	Transitional endoplasmic reticulum ATPase	VCP HEL-220 HEL-S-70	Homo sapiens (human)	3	1
P29401	Transketolase	TKT	Homo sapiens (human)	2	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 Crohn's colitis Crohn's disease Leigh disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Wernicke encephalopathy Wernicke-Korsakoff syndrome adenocarcinoma adenoma adrenal cortex cancer alcohol dependence alcohol use disorder amnestic disorder atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect beriberi breast cancer breast carcinoma cancer carcinoma central nervous system cancer cerebral degeneration cervical adenocarcinoma cervical cancer cervix carcinoma chronic kidney disease chronic myeloid leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer cribriform carcinoma critical illness polyneuropathy cystinuria diabetes mellitus diabetic autonomic neuropathy diabetic ketoacidosis diabetic neuropathy diabetic polyneuropathy dry beriberi embryoma galactosemia gallbladder disease giant cell glioblastoma glioblastoma gliosarcoma glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease granular cell carcinoma hepatitis B hepatocellular carcinoma high grade glioma hyperglycemia inflammatory and toxic neuropathy inflammatory bowel disease 1 inflammatory bowel disease inherited metabolic disorder insulinoma intellectual disability large intestine cancer learning disability liver cancer liver disease meningoencephalitis mixed glioma multiple sclerosis myeloproliferative disorder with eosinophilia nasopharynx carcinoma neurodegenerative disease neuropathy obsolete type 1 diabetes mellitus 9 ovarian cancer ovarian carcinoma patent ductus arteriosus patent foramen ovale pellagra peripheral nervous system disease polyneuropathy rectal benign neoplasm rectum adenocarcinoma rectum cancer sarcomatoid carcinoma schizophrenia stereotypic movement disorder stomach cancer stomach carcinoma thiamine deficiency disease thiamine-responsive megaloblastic anemia syndrome thyroid gland anaplastic carcinoma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis 1 tuberous sclerosis tubular adenocarcinoma 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 ventricular septal defect
Q8N442	Translation factor GUF1, mitochondrial	GUF1	Homo sapiens (human)	0	1
P46199	Translation initiation factor IF-2, mitochondrial	MTIF2	Homo sapiens (human)	0	1
O75794	Translation initiation factor eIF2 assembly protein	CDC123 C10orf7 D123	Homo sapiens (human)	0	1
Q14232	Translation initiation factor eIF2B subunit alpha	EIF2B1 EIF2BA	Homo sapiens (human)	1	1

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