GlyCosmos Portal

Displaying entries **16426 - 16450** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
O00567	Nucleolar protein 56	NOP56 NOL5A	5	5
Q8TDX6	Chondroitin sulfate N-acetylgalactosaminyltransferase 1	CSGALNACT1 CHGN GALNACT1	5	4	Guillain-Barre syndrome Laron syndrome Miller Fisher syndrome achondroplasia anorexia nervosa breast cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer diabetic ketoacidosis large intestine cancer melanoma multiple sclerosis obsolete type 1 diabetes mellitus 9 skin melanoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus
Q93070	Ecto-ADP-ribosyltransferase 4	ART4 DO DOK1	5	23	carotid artery thrombosis carotid stenosis conjunctivitis
Q9BU40	Chordin-like protein 1	CHRDL1 NRLN1	5	5
Q96D42	Hepatitis A virus cellular receptor 1	HAVCR1 KIM1 TIM1 TIMD1	5	5
Q14416	Metabotropic glutamate receptor 2	GRM2 GPRC1B MGLUR2	5	0
P81877	Single-stranded DNA-binding protein 2	SSBP2 SSDP2	5	1
Q6FHJ7	Secreted frizzled-related protein 4	SFRP4 FRPHE	5	31
Q8TE59	A disintegrin and metalloproteinase with thrombospondin motifs 19	ADAMTS19	5	0
Q16581	C3a anaphylatoxin chemotactic receptor	C3AR1 AZ3B C3R1 HNFAG09	5	2
B5A929	Soluble MET variant 1	MET	5	0
Q96KG7	Multiple epidermal growth factor-like domains protein 10	MEGF10 KIAA1780	5	0
Q96HA4	Uncharacterized protein C1orf159	C1orf159	5	3
Q68CP4	Heparan-alpha-glucosaminide N-acetyltransferase	HGSNAT TMEM76	5	19	Zollinger-Ellison syndrome agnosia amnestic disorder blindness bulimia nervosa cataract cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness corneal disease developmental coordination disorder diabetes mellitus diarrhea dissociated nystagmus echolalia enterocele epilepsy fundus albipunctatus fundus dystrophy glaucoma hyperinsulinism hypertrichosis hypertrophic cardiomyopathy 1 hypogonadism intellectual disability keratoconus learning disability mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis night blindness obesity obsolete asthenopia ophthalmoplegia optic atrophy pathologic nystagmus peripheral retinal degeneration retinitis pigmentosa 73 retinitis pigmentosa retrograde amnesia scoliosis sensorineural hearing loss spontaneous ocular nystagmus stereotypic movement disorder type 2 diabetes mellitus visual epilepsy
Q9H156	SLIT and NTRK-like protein 2	SLITRK2 CXorf2 KIAA1854 SLITL1	5	2
P78559	Microtubule-associated protein 1A	MAP1A MAP1L	5	1
Q8IVW6	AT-rich interactive domain-containing protein 3B	ARID3B BDP DRIL2	5	2
A6NGN9	IgLON family member 5	IGLON5	5	0
P23769	Endothelial transcription factor GATA-2	GATA2	5	1
Q9NZM1	Myoferlin	MYOF FER1L3 KIAA1207	5	2
P08195	Amino acid transporter heavy chain SLC3A2	SLC3A2 MDU1	5	147
P29323	Ephrin type-B receptor 2	EPHB2 DRT EPHT3 EPTH3 ERK HEK5 TYRO5	5	3
Q9UPP1	Histone lysine demethylase PHF8	PHF8 KIAA1111 ZNF422	5	2
O75718	Cartilage-associated protein	CRTAP CASP	5	22
Q92917	G-patch domain and KOW motifs-containing protein	GPKOW GPATC5 GPATCH5 T54	5	1

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