GlyCosmos Portal

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UniProt ID	Protein Name ▼	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q15080	Neutrophil cytosol factor 4	NCF4 SH3PXD4	0	1
P19878	Neutrophil cytosol factor 2	NCF2 NOXA2 P67PHOX	0	1
P22894	Neutrophil collagenase	MMP8 CLG1	5	0
Q6PIU2	Neutral cholesterol ester hydrolase 1	NCEH1 AADACL1 KIAA1363	4	23
Q9NR71	Neutral ceramidase	ASAH2 HNAC1	23	0	Alzheimer's disease autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome celiac disease colorectal cancer congenital diaphragmatic hernia cystic fibrosis dementia diabetes mellitus diabetic ketoacidosis gallbladder disease gamma heavy chain disease glaucoma heavy chain disease inflammatory bowel disease large intestine cancer liver disease lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 neuroblastoma obesity systemic Epstein-Barr virus positive T-cell lymphoma of childhood type 2 diabetes mellitus
Q6YBV0	Neutral amino acid uniporter 4	SLC36A4 PAT4	3	3
Q15758	Neutral amino acid transporter B(0)	SLC1A5 ASCT2 M7V1 RDR RDRC	2	12
P43007	Neutral amino acid transporter A	SLC1A4 ASCT1 SATT	2	3
Q8NBW4	Neutral amino acid transporter 9	SLC38A9 URLC11	4	0
Q8TET4	Neutral alpha-glucosidase C	GANC	0	1	congenital dyserythropoietic anemia panic disorder
Q14697	Neutral alpha-glucosidase AB	GANAB G2AN KIAA0088	3	6	Meckel syndrome arthritis arthropathy autosomal dominant polycystic kidney disease chronic fatigue syndrome encephalitis encephalomyelitis gallbladder disease liver disease multiple sclerosis myelitis osteoarthritis polycystic kidney disease 1 polycystic kidney disease 2 polycystic kidney disease 3 polycystic liver disease
P56730	Neurotrypsin	PRSS12	2	0
P34130	Neurotrophin-4	NTF4 NTF5	1	0
P20783	Neurotrophin-3	NTF3	1	0
Q9P121	Neurotrimin	NTM IGLON2 NT	7	0	Kartagener syndrome Mycobacterium avium complex disease Parkinson's disease acquired immunodeficiency syndrome actinic keratosis acute myeloid leukemia acute myocardial infarction attention deficit hyperactivity disorder autism spectrum disorder autistic disorder bronchiectasis cancer chronic obstructive pulmonary disease congenital aphakia congenital heart disease congestive heart failure coronary thrombosis depressive disorder embryoma endophthalmitis esophagitis familial medullary thyroid carcinoma gallbladder disease gastroesophageal reflux disease hepatocellular carcinoma intracranial aneurysm late onset Parkinson's disease leprosy liver cancer liver disease lung disease lymphadenitis major depressive disorder melancholic depression multiple endocrine neoplasia type 2A myocardial infarction myopia neurotic disorder nicotine dependence obsolete melancholia peptic esophagitis primary ciliary dyskinesia 1 primary ciliary dyskinesia primary open angle glaucoma pulmonary tuberculosis schizophrenia seborrheic keratosis silent myocardial infarction skin disease thyroid gland medullary carcinoma tuberculosis tuberculous pneumothorax
P30989	Neurotensin receptor type 1	NTSR1 NTRR	3	0
Q99574	Neuroserpin	SERPINI1 PI12	4	16
O15240	Neurosecretory protein VGF	VGF	14	2
Q9Y639	Neuroplastin	NPTN SDFR1 SDR1	8	37
O60462	Neuropilin-2	NRP2 VEGF165R2	13	2
O14786	Neuropilin-1	NRP1 NRP VEGF165R	17	58
Q8NC67	Neuropilin and tolloid-like protein 2	NETO2 BTCL2	3	2
Q8TDF5	Neuropilin and tolloid-like protein 1	NETO1 BTCL1	3	1
X5D7M1	Neuropilin 2 isoform B (Fragment)	NRP2	2	0
V9GYL7	Neuropilin 1 (Fragment)	NRP1	1	0

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