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 **17676 - 17700** 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
P12036	Neurofilament heavy polypeptide	NEFH KIAA0845 NFH	Homo sapiens (human)	11	1
Q99435	Protein kinase C-binding protein NELL2	NELL2 NRP2	Homo sapiens (human)	11	3
Q96MS0	Roundabout homolog 3	ROBO3	Homo sapiens (human)	11	1
Q9BTA9	WW domain-containing adapter protein with coiled-coil	WAC KIAA1844	Homo sapiens (human)	11	1
O43852	Calumenin	CALU	Homo sapiens (human)	11	116
Q9Y4H2	Insulin receptor substrate 2	IRS2	Homo sapiens (human)	11	1
Q9Y493	Zonadhesin	ZAN	Homo sapiens (human)	11	1
O75578	Integrin alpha-10	ITGA10	Homo sapiens (human)	11	0
Q8NHP8	Putative phospholipase B-like 2	PLBD2	Homo sapiens (human)	11	22
Q96PQ1	Sialic acid-binding Ig-like lectin 12	SIGLEC12 SIGLECL1 SLG	Homo sapiens (human)	11	1	carcinoma chronic fatigue syndrome disease of metabolism encephalomyelitis obesity prostate cancer prostate carcinoma sarcomatoid carcinoma systemic lupus erythematosus
Q69384	Endogenous retrovirus group K member 6 Env polyprotein	ERVK-6 ERVK6	Homo sapiens (human)	11	0
Q9NY47	Voltage-dependent calcium channel subunit alpha-2/delta-2	CACNA2D2 KIAA0558	Homo sapiens (human)	11	6	absence epilepsy agnosia alternating hemiplegia of childhood autonomic neuropathy bipolar I disorder brain cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system disease cerebellar ataxia cerebellar disease cervical adenocarcinoma cervical cancer cervix carcinoma cervix uteri carcinoma in situ childhood absence epilepsy choreatic disease colorectal cancer colorectal carcinoma congenital nystagmus coronary artery disease developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 21 dissociated nystagmus embryoma epilepsy hypertropia idiopathic generalized epilepsy large intestine cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma maple syrup urine disease mechanical strabismus nasopharynx carcinoma nervous system disease ophthalmoplegia pathologic nystagmus primary cutaneous amyloidosis prostate cancer prostate carcinoma sensorineural hearing loss sick sinus syndrome spontaneous ocular nystagmus strabismus syndromic X-linked intellectual disability type 10
Q8NEZ2	Vacuolar protein sorting-associated protein 37A	VPS37A HCRP1	Homo sapiens (human)	11	2
Q12805	EGF-containing fibulin-like extracellular matrix protein 1	EFEMP1 FBLN3 FBNL	Homo sapiens (human)	11	7
P52799	Ephrin-B2	EFNB2 EPLG5 HTKL LERK5	Homo sapiens (human)	11	17
O43524	Forkhead box protein O3	FOXO3 FKHRL1 FOXO3A	Homo sapiens (human)	11	2
Q9UKH3	Endogenous retrovirus group K member 9 Env polyprotein	ERVK-9	Homo sapiens (human)	11	0
Q12860	Contactin-1	CNTN1	Homo sapiens (human)	11	21	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 Compton-North congenital myopathy Guillain-Barre syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease Miller Fisher syndrome Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome adenocarcinoma adenoma arthritis arthropathy attention deficit hyperactivity disorder breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral degeneration chronic inflammatory demyelinating polyneuritis chronic inflammatory demyelinating polyradiculoneuropathy colorectal cancer colorectal carcinoma congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital myopathy 1A craniosynostosis cribriform carcinoma embryoma esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma familial adenomatous polyposis 1 familial adenomatous polyposis familial nephrotic syndrome familial periodic paralysis fetal akinesia deformation sequence syndrome 1 fetal akinesia deformation sequence syndrome gliosarcoma granular cell carcinoma high grade glioma islet cell tumor large intestine cancer lipoid nephrosis lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lung small cell carcinoma megaconial type congenital muscular dystrophy membranous glomerulonephritis mixed glioma multiple sclerosis muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 myopathy nemaline myopathy nephrotic syndrome neuropathy peripheral nervous system disease placental insufficiency polyhydramnios polyneuropathy progressive muscular atrophy prostate cancer prostate carcinoma rigid spine muscular dystrophy 1 spinal muscular atrophy squamous cell carcinoma stomach cancer stomach carcinoma thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma tubular adenocarcinoma
Q9HC78	Zinc finger and BTB domain-containing protein 20	ZBTB20 DPZF ZNF288	Homo sapiens (human)	11	2
Q9Y467	Sal-like protein 2	SALL2 KIAA0360 SAL2 ZNF795	Homo sapiens (human)	11	2
P31997	Carcinoembryonic antigen-related cell adhesion molecule 8	CEACAM8 CGM6	Homo sapiens (human)	11	10
Q13761	Runt-related transcription factor 3	RUNX3 AML2 CBFA3 PEBP2A3	Homo sapiens (human)	11	1
Q9ULH7	Myocardin-related transcription factor B	MRTFB KIAA1243 MKL2	Homo sapiens (human)	11	1
Q8IVL1	Neuron navigator 2	NAV2 HELAD1 KIAA1419 POMFIL2 RAINB1 STEERIN2	Homo sapiens (human)	11	18
Q8NBJ9	SID1 transmembrane family member 2	SIDT2	Homo sapiens (human)	11	8

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