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 **5301 - 5325** 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
Q86VS3	IQ domain-containing protein H	IQCH	Homo sapiens (human)	1	1
Q8N0W5	IQ domain-containing protein K	IQCK	Homo sapiens (human)	0	1
Q9H0B3	IQ domain-containing protein N	IQCN KIAA1683	Homo sapiens (human)	0	1
Q6DN90	IQ motif and SEC7 domain-containing protein 1	IQSEC1 ARFGEP100 BRAG2 KIAA0763	Homo sapiens (human)	0	1
Q5JU85	IQ motif and SEC7 domain-containing protein 2	IQSEC2 KIAA0522	Homo sapiens (human)	2	3
Q9UPP2	IQ motif and SEC7 domain-containing protein 3	IQSEC3 KIAA1110	Homo sapiens (human)	1	1
A8MXQ7	IQ motif and ankyrin repeat domain-containing protein 1	IQANK1	Homo sapiens (human)	0	1
P53990	IST1 homolog	IST1 KIAA0174	Homo sapiens (human)	0	1
A5YM53	ITGAV protein	ITGAV	Homo sapiens (human)	2	0
B7ZKJ8	ITIH4 protein	ITIH4	Homo sapiens (human)	3	0
P22304	Iduronate 2-sulfatase	IDS SIDS	Homo sapiens (human)	9	9	Balo concentric sclerosis Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome Fabry disease Griscelli syndrome type 1 Griscelli syndrome type 2 Griscelli syndrome type 3 Griscelli syndrome Laron syndrome Marfan syndrome Sveinsson chorioretinal atrophy Waardenburg syndrome type 3 X-linked ichthyosis achondroplasia adrenoleukodystrophy agammaglobulinemia allergic asthma alternating hemiplegia of childhood amnestic disorder antiphospholipid syndrome asthma autism spectrum disorder autistic disorder autonomic neuropathy bone marrow cancer brain disease breast cancer breast carcinoma cancer central nervous system disease centronuclear myopathy X-linked centronuclear myopathy cerebral infarction cerebrovascular disease chronic obstructive pulmonary disease chylomicron retention disease communicating hydrocephalus congenital adrenal hyperplasia congenital central hypoventilation syndrome congenital ptosis congenital structural myopathy congestive heart failure craniosynostosis cystinuria depressive disorder diarrhea dysthymic disorder embryoma epilepsy fragile X syndrome galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease Ia glycogen storage disease glycoproteinosis heart valve disease hydrocephalus hypercalcemia hypertrichosis hypoglycemia inguinal hernia intellectual disability intrinsic asthma learning disability lipid storage disease lung benign neoplasm lung carcinoma lysosomal storage disease major depressive disorder melancholic depression metachromatic leukodystrophy mixed sleep apnea mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis myeloproliferative neoplasm myocarditis myotonic disease myotonic dystrophy type 2 narcolepsy nephrocalcinosis nervous system disease neurotic disorder obsolete intestinal pseudo-obstruction obsolete melancholia obstructive hydrocephalus obstructive sleep apnea ocular albinism with sensorineural deafness oculocutaneous albinism omphalocele optic papillitis osteochondrodysplasia ovarian cancer ovarian carcinoma pancytopenia papilledema paralytic ileus phosphorus metabolism disease post-traumatic stress disorder ptosis retinal edema retrograde amnesia rumination disorder senile degeneration of brain sensorineural hearing loss sick sinus syndrome situs inversus sleep apnea sudden infant death syndrome trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis umbilical hernia visual epilepsy
A6NFU0	Ig-like V-type domain-containing protein FAM187A	FAM187A	Homo sapiens (human)	1	0
P55899	IgG receptor FcRn large subunit p51	FCGRT FCRN	Homo sapiens (human)	2	49
Q9Y6R7	IgGFc-binding protein	FCGBP	Homo sapiens (human)	20	47
A6NGN9	IgLON family member 5	IGLON5	Homo sapiens (human)	5	0
Q12908	Ileal sodium/bile acid cotransporter	SLC10A2 ASBT ISBT NTCP2	Homo sapiens (human)	1	0
Q9GZP8	Immortalization up-regulated protein	IMUP C19orf33	Homo sapiens (human)	0	1
Q8WZA9	Immunity-related GTPase family Q protein	IRGQ IRGQ1	Homo sapiens (human)	0	1
P01591	Immunoglobulin J chain	JCHAIN IGCJ IGJ	Homo sapiens (human)	6	165
P24071	Immunoglobulin alpha Fc receptor	FCAR CD89	Homo sapiens (human)	5	0
P01876	Immunoglobulin heavy constant alpha 1	IGHA1	Homo sapiens (human)	14	219
P01877	Immunoglobulin heavy constant alpha 2	IGHA2	Homo sapiens (human)	6	168
P01880	Immunoglobulin heavy constant delta	IGHD	Homo sapiens (human)	11	102
P01854	Immunoglobulin heavy constant epsilon	IGHE	Homo sapiens (human)	7	126
P01857	Immunoglobulin heavy constant gamma 1	IGHG1	Homo sapiens (human)	2	208

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