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 **1876 - 1900** 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
Q9NPB9	Atypical chemokine receptor 4	ACKR4 CCBP2 CCR11 CCRL1 VSHK1	Homo sapiens (human)	2	0
Q9NPA9	Rheumatoid arthritis-related antigen RA-A47 (Fragment)	ra-a47	Homo sapiens (human)	2	0
Q9NPA8	Transcription and mRNA export factor ENY2	ENY2	Homo sapiens (human)	0	1
Q9NPA3	Mid1-interacting protein 1	MID1IP1 MIG12	Homo sapiens (human)	0	1
Q9NPA2	Matrix metalloproteinase-25	MMP25 MMP20 MMPL1 MT6MMP	Homo sapiens (human)	1	1	X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2 acoustic neuroma acute pericementitis adult fibrosarcoma aggressive periodontitis amelogenesis imperfecta hypomaturation type 2A2 amelogenesis imperfecta hypomaturation type 2A3 amelogenesis imperfecta hypomaturation type 2A4 amelogenesis imperfecta hypomaturation type 2A5 amelogenesis imperfecta type 1A amelogenesis imperfecta type 1B amelogenesis imperfecta type 1C amelogenesis imperfecta type 1E amelogenesis imperfecta type 1F amelogenesis imperfecta type 1G amelogenesis imperfecta type 1H amelogenesis imperfecta type 2A1 amelogenesis imperfecta type 3A amelogenesis imperfecta type 4 amelogenesis imperfecta anaplastic astrocytoma angiomatous meningioma arthritis arthropathy benign meningioma brain cancer breast cancer breast carcinoma cancer carcinoma cerebral convexity meningioma childhood cerebral astrocytoma clear cell meningioma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer dental fluorosis dentin dysplasia dentinogenesis imperfecta embryoma fibrillary astrocytoma fibrosarcoma fibrous meningioma gemistocytic astrocytoma giant cell glioblastoma glioblastoma in situ carcinoma intraorbital meningioma intraventricular meningioma juvenile pilocytic astrocytoma large intestine cancer laryngeal squamous cell carcinoma malignant astrocytoma melanoma meningioma meningothelial meningioma microcystic meningioma multiple myeloma multiple sclerosis olfactory groove meningioma osteoarthritis parasagittal meningioma periodontosis pilocytic astrocytoma pituitary adenoma protoplasmic astrocytoma psammomatous meningioma rheumatoid arthritis sarcomatoid carcinoma secretory meningioma skin melanoma spinal meningioma stomach cancer stomach carcinoma subependymal giant cell astrocytoma transitional meningioma
Q9NPA1	Calcium-activated potassium channel subunit beta-3	KCNMB3 KCNMB2 KCNMBL	Homo sapiens (human)	1	0
Q9NPA0	Endoplasmic reticulum membrane protein complex subunit 7	EMC7 C11orf3 C15orf24	Homo sapiens (human)	3	2
Q9NP99	Triggering receptor expressed on myeloid cells 1	TREM1	Homo sapiens (human)	3	0
Q9NP92	Large ribosomal subunit protein mL65	MRPS30 PDCD9	Homo sapiens (human)	0	1
Q9NP91	Sodium- and chloride-dependent transporter XTRP3	SLC6A20 SIT1 XT3 XTRP3	Homo sapiens (human)	2	0
Q9NP85	Podocin	NPHS2	Homo sapiens (human)	1	0
Q9NP81	Serine--tRNA ligase, mitochondrial	SARS2 SARSM	Homo sapiens (human)	1	1
Q9NP80	Calcium-independent phospholipase A2-gamma	PNPLA8 IPLA22 IPLA2G	Homo sapiens (human)	3	1
Q9NP79	Vacuolar protein sorting-associated protein VTA1 homolog	VTA1 C6orf55	Homo sapiens (human)	1	1
Q9NP78	ABC-type oligopeptide transporter ABCB9	ABCB9 KIAA1520	Homo sapiens (human)	2	1
Q9NP77	RNA polymerase II subunit A C-terminal domain phosphatase SSU72	SSU72	Homo sapiens (human)	0	1
Q9NP73	UDP-N-acetylglucosamine transferase subunit ALG13	ALG13 CXorf45 GLT28D1	Homo sapiens (human)	0	1	Bell's palsy Meckel's diverticulum West syndrome agnosia attention deficit hyperactivity disorder autistic disorder blindness cerebral degeneration choreatic disease clubfoot congenital disorder of glycosylation type I congenital disorder of glycosylation congenital nystagmus craniosynostosis developmental and epileptic encephalopathy 36 dissociated nystagmus epilepsy facial nerve disease facial paralysis focal segmental glomerulosclerosis hypophosphatemia intellectual disability learning disability lung cancer lung non-small cell carcinoma microcephaly non-syndromic X-linked intellectual disability obesity obsolete infantile epileptic encephalopathy optic atrophy pathologic nystagmus placental insufficiency pyloric stenosis spontaneous ocular nystagmus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 visual epilepsy
Q9NP71	Carbohydrate-responsive element-binding protein	MLXIPL BHLHD14 MIO WBSCR14	Homo sapiens (human)	8	1
Q9NP70	Ameloblastin	AMBN	Homo sapiens (human)	1	0
Q9NP66	High mobility group protein 20A	HMG20A HMGX1 HMGXB1	Homo sapiens (human)	0	1
Q9NP64	Zinc finger CCHC domain-containing protein 17	ZCCHC17 PS1D	Homo sapiens (human)	0	1
Q9NP62	Chorion-specific transcription factor GCMa	GCM1 GCMA	Homo sapiens (human)	1	1
Q9NP61	ADP-ribosylation factor GTPase-activating protein 3	ARFGAP3 ARFGAP1	Homo sapiens (human)	3	2
Q9NP60	X-linked interleukin-1 receptor accessory protein-like 2	IL1RAPL2 IL1R9	Homo sapiens (human)	5	0	autism spectrum disorder autistic disorder breast cancer childhood type dermatomyositis dermatomyositis hepatitis C myositis
Q9NP59	Solute carrier family 40 member 1	SLC40A1 FPN FPN1 IREG1 SLC11A3	Homo sapiens (human)	1	1

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