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 **1301 - 1325** 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
A0A6Q8PG06	Carboxypeptidase B2	CPB2	Homo sapiens (human)	3	0
Q8N6Y1	Protocadherin-20	PCDH20 PCDH13	Homo sapiens (human)	8	2
Q9HC36	rRNA methyltransferase 3, mitochondrial	MRM3 RNMTL1	Homo sapiens (human)	1	1
P01019	Angiotensinogen	AGT SERPINA8	Homo sapiens (human)	9	69
Q99081	Transcription factor 12	TCF12 BHLHB20 HEB HTF4	Homo sapiens (human)	8	1
O94813	Slit homolog 2 protein	SLIT2 SLIL3	Homo sapiens (human)	12	13
A0A7T8GE73	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
O00590	Atypical chemokine receptor 2	ACKR2 CCBP2 CCR10 CMKBR9 D6	Homo sapiens (human)	1	0
A0A7P0T9G9	cathepsin X	CTSZ	Homo sapiens (human)	1	0
Q04656	Copper-transporting ATPase 1	ATP7A MC1 MNK	Homo sapiens (human)	3	2
P20061	Transcobalamin-1	TCN1 TC1	Homo sapiens (human)	9	11
O14980	Exportin-1	XPO1 CRM1	Homo sapiens (human)	1	1
A8MPX8	Protein phosphatase 2C-like domain-containing protein 1	PP2D1 C3orf48	Homo sapiens (human)	0	1
P23434	Glycine cleavage system H protein, mitochondrial	GCSH	Homo sapiens (human)	0	1	Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome Unverricht-Lundborg syndrome X-linked Aarskog syndrome autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome blepharospasm brain disease breast cancer breast carcinoma cancer central nervous system lymphoma chondrodysplasia-pseudohermaphroditism syndrome early myoclonic encephalopathy embryoma epilepsy focal hand dystonia glycine encephalopathy intellectual disability learning disability lymphoma microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II obsolete ymphosarcoma schizophrenia urea cycle disorder visual epilepsy
A0A0C4ZLK5	HLA-B protein (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q92854	Semaphorin-4D	SEMA4D C9orf164 CD100 SEMAJ	Homo sapiens (human)	20	41
P78314	SH3 domain-binding protein 2	SH3BP2 3BP2	Homo sapiens (human)	0	1
A0A0G2R0X4	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
A6NFU0	Ig-like V-type domain-containing protein FAM187A	FAM187A	Homo sapiens (human)	1	0
Q9BUG6	Zinc finger and SCAN domain-containing protein 5A	ZSCAN5A ZNF495 ZSCAN5	Homo sapiens (human)	4	1
A0A0N7A4F5	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
E2GJH7	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
O60245	Protocadherin-7	PCDH7 BHPCDH	Homo sapiens (human)	9	3
A0A0A7C5N3	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
A0A0K0KS59	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0

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