GlyCosmos Portal

Displaying entries **6501 - 6525** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
Q9UPM6	LIM/homeobox protein Lhx6	LHX6 LHX6.1	0	1
P05161	Ubiquitin-like protein ISG15	ISG15 G1P2 UCRP	0	1
E9PRG8	Uncharacterized protein C11orf98	C11orf98	0	1
P41743	Protein kinase C iota type	PRKCI DXS1179E	0	1
Q9H2Z4	Homeobox protein Nkx-2.4	NKX2-4 NKX2D	0	1
Q8TBZ5	Zinc finger protein 502	ZNF502	1	1
Q96JC9	ELL-associated factor 1	EAF1	1	1
Q9H693	Uncharacterized protein C16orf95	C16orf95	1	1
O94991	SLIT and NTRK-like protein 5	SLITRK5 KIAA0918 LRRC11	4	1
Q9Y330	Zinc finger and BTB domain-containing protein 12	ZBTB12 C6orf46 G10 NG35	0	1
Q96AH0	SOSS complex subunit B2	NABP1 OBFC2A SSB2	1	1
Q8N6N3	UPF0690 protein C1orf52	C1orf52 BAG	0	1
Q9BWW4	Single-stranded DNA-binding protein 3	SSBP3 SSDP SSDP1	3	1
Q9Y3B4	Splicing factor 3B subunit 6	SF3B6 SAP14 SF3B14 SF3B14A	0	1
Q86VH2	Kinesin-like protein KIF27	KIF27	2	1
P55072	Transitional endoplasmic reticulum ATPase	VCP HEL-220 HEL-S-70	3	1
Q16650	T-box brain protein 1	TBR1	1	1
Q96MK2	RIPOR family member 3	RIPOR3 C20orf175 C20orf176 FAM65C	1	1
P63119	Endogenous retrovirus group K member 21 Pro protein	ERVK-21	3	1
P07766	T-cell surface glycoprotein CD3 epsilon chain	CD3E T3E	1	1
Q00577	Transcriptional activator protein Pur-alpha	PURA PUR1	0	1
Q69YQ0	Cytospin-A	SPECC1L CYTSA KIAA0376	2	1
Q9HCK1	DBF4-type zinc finger-containing protein 2	ZDBF2 KIAA1571	4	1
Q15147	1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase beta-4	PLCB4	0	1	46,XY sex reversal Chagas disease Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Kawasaki disease abdominal obesity-metabolic syndrome 1 absence epilepsy acute chest syndrome acute myeloid leukemia adenocarcinoma adenoma agenesis of the corpus callosum with peripheral neuropathy agnosia ankylosis bipolar disorder breast cancer breast carcinoma cancer central sleep apnea childhood absence epilepsy childhood acute myeloid leukemia cleft palate congenital ptosis coronary aneurysm cribriform carcinoma cutaneous fibrous histiocytoma dengue hemorrhagic fever depressive disorder embryoma endometriosis of uterus endometriosis essential thrombocythemia gastrointestinal stromal tumor granular cell carcinoma hereditary neuropathy with liability to pressure palsies hidradenoma isolated cleft palate lung cancer lung non-small cell carcinoma major depressive disorder melancholic depression melanoma mood disorder motor peripheral neuropathy myelodysplastic syndrome neurotic disorder obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obstructive sleep apnea ptosis schizoaffective disorder schizophrenia schizophreniform disorder sensorineural hearing loss skin melanoma skin papilloma skin tag syringoma tongue disease trypanosomiasis tubular adenocarcinoma uveal melanoma
Q9Y3R5	Protein dopey-2	DOP1B C21orf5 DOPEY2 KIAA0933	0	1

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