GlyCosmos Portal

Displaying entries **12576 - 12600** of **18496** in total

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UniProt ID ▲	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q7L4I2	Arginine/serine-rich coiled-coil protein 2	RSRC2	0	1
Q7L4P6	BEN domain-containing protein 5	BEND5 C1orf165	0	1
Q7L513	Fc receptor-like A	FCRLA FCRL FCRL1 FCRLM1 FCRX FREB	1	1
Q7L576	Cytoplasmic FMR1-interacting protein 1	CYFIP1 KIAA0068	1	2
Q7L590	Protein MCM10 homolog	MCM10	1	1
Q7L591	Docking protein 3	DOK3	1	1
Q7L592	Protein arginine methyltransferase NDUFAF7, mitochondrial	NDUFAF7 C2orf56	3	1
Q7L5A8	Fatty acid 2-hydroxylase	FA2H FAAH FAXDC1	1	1
Q7L5L3	Lysophospholipase D GDPD3	GDPD3 GDE7	0	1	Fabry disease Wolman disease chylomicron retention disease lipid storage disease
Q7L5N1	COP9 signalosome complex subunit 6	COPS6 CSN6 HVIP	0	1
Q7L5N7	Lysophosphatidylcholine acyltransferase 2	LPCAT2 AGPAT11 AYTL1	0	1	colorectal cancer colorectal carcinoma large intestine cancer microphthalmia obsolete Matthew-Wood syndrome polycystic ovary syndrome prostate cancer prostate carcinoma
Q7L5Y1	Mitochondrial enolase superfamily member 1	ENOSF1 RTS TYMSAS	0	1	Down syndrome Hailey-Hailey disease Holt-Oram syndrome Klippel-Trenaunay syndrome Marfan syndrome Plasmodium falciparum malaria Rothmund-Thomson syndrome Rubinstein-Taybi syndrome VACTERL association Werner syndrome adult lymphoma arachnoiditis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB cancer central nervous system cancer central nervous system lymphoma cerebral malaria childhood leukemia childhood lymphoma colorectal cancer colorectal carcinoma congenital central hypoventilation syndrome cutaneous mastocytosis cutis laxa diffuse cutaneous mastocytosis embryoma endometrial cancer endometrial carcinoma exanthem gliosarcoma hepatitis B herpes zoster high grade glioma intellectual disability large intestine cancer learning disability leukemia lymphoma mal de Meleda malaria mastocytosis meningitis microphthalmia with limb anomalies mixed glioma mixed sleep apnea nail-patella syndrome obsolete ymphosarcoma obstructive sleep apnea ovarian cancer ovarian carcinoma poikiloderma with neutropenia progeria rabies restrictive dermopathy situs inversus sleep apnea split hand-foot malformation 1 with sensorineural hearing loss stomach cancer stomach carcinoma thrombocytopenia-absent radius syndrome tuberous sclerosis urticaria pigmentosa uterine corpus cancer
Q7L5Y6	DET1 homolog	DET1	0	1
Q7L775	EPM2A-interacting protein 1	EPM2AIP1 KIAA0766	0	1
Q7L7L0	Histone H2A type 3	H2AC25 H2AW HIST3H2A	1	1
Q7L7X3	Serine/threonine-protein kinase TAO1	TAOK1 KIAA1361 MAP3K16 MARKK	2	1
Q7L804	Rab11 family-interacting protein 2	RAB11FIP2 KIAA0941	0	1
Q7L8A9	Tubulinyl-Tyr carboxypeptidase 1	VASH1 KIAA1036 VASH	1	1
Q7L8C5	Synaptotagmin-13	SYT13 KIAA1427	3	3
Q7L8L6	FAST kinase domain-containing protein 5, mitochondrial	FASTKD5 KIAA1792	0	1
Q7L8S5	OTU domain-containing protein 6A	OTUD6A DUBA2	1	1
Q7L8W6	Diphthine--ammonia ligase	DPH6 ATPBD4	0	1
Q7L945	Zinc finger protein 627	ZNF627	0	1
Q7L985	Leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 2	LINGO2 LERN3 LRRN6C	5	0
Q7L9L4	MOB kinase activator 1B	MOB1B MOB4A MOBKL1A	0	1

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