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 **2476 - 2500** 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
Q9NZM1	Myoferlin	MYOF FER1L3 KIAA1207	Homo sapiens (human)	5	2
P08195	Amino acid transporter heavy chain SLC3A2	SLC3A2 MDU1	Homo sapiens (human)	5	147
P29323	Ephrin type-B receptor 2	EPHB2 DRT EPHT3 EPTH3 ERK HEK5 TYRO5	Homo sapiens (human)	5	3
Q9UPP1	Histone lysine demethylase PHF8	PHF8 KIAA1111 ZNF422	Homo sapiens (human)	5	2
O75718	Cartilage-associated protein	CRTAP CASP	Homo sapiens (human)	5	22
Q92917	G-patch domain and KOW motifs-containing protein	GPKOW GPATC5 GPATCH5 T54	Homo sapiens (human)	5	1
E5RIL1	Uroplakin-3b-like protein 2	UPK3BL2	Homo sapiens (human)	5	0
Q6UWV6	Ectonucleotide pyrophosphatase/phosphodiesterase family member 7	ENPP7	Homo sapiens (human)	5	14	adenocarcinoma adenoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis cancer colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease cystic fibrosis familial adenomatous polyposis 1 familial adenomatous polyposis follicular adenoma islet cell tumor large intestine cancer microcystic adenoma papillary adenoma
G3V595	Serpin family A member 3 (Fragment)	SERPINA3	Homo sapiens (human)	5	0
P78364	Polyhomeotic-like protein 1	PHC1 EDR1 PH1	Homo sapiens (human)	5	1
Q8NBJ5	Procollagen galactosyltransferase 1	COLGALT1 GLT25D1	Homo sapiens (human)	5	31	Balo concentric sclerosis Simpson-Golabi-Behmel syndrome type 1 adrenoleukodystrophy bone osteosarcoma central nervous system disease cerebral degeneration childhood osteosarcoma epilepsy locked-in syndrome narcolepsy osteosarcoma porencephaly quadriplegia visual epilepsy
P04080	Cystatin-B	CSTB CST6 STFB	Homo sapiens (human)	5	1
Q9UKF2	Disintegrin and metalloproteinase domain-containing protein 30	ADAM30	Homo sapiens (human)	5	0
B0FP48	Uroplakin-3b-like protein 1	UPK3BL1 UPLP	Homo sapiens (human)	5	4
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
P04066	Tissue alpha-L-fucosidase	FUCA1	Homo sapiens (human)	5	53	Laron syndrome Sjogren's syndrome achondroplasia acquired immunodeficiency syndrome angiokeratoma anhidrosis aspartylglucosaminuria autoimmune disease autoimmune lymphoproliferative syndrome breast cancer breast carcinoma cancer cerebral degeneration colorectal cancer colorectal carcinoma congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital hypothyroidism craniosynostosis critical illness polyneuropathy diabetic cataract diabetic retinopathy embryoma enterocele epilepsy fucosidosis head and neck cancer human immunodeficiency virus infectious disease hypertrichosis hypohidrosis hypothyroidism immune system disease inflammatory and toxic neuropathy intellectual disability keratoconjunctivitis sicca large intestine cancer learning disability lipoatrophic diabetes mellitus lipodystrophy livedoid vasculitis lobular neoplasia locked-in syndrome lysosomal storage disease meningoencephalitis mucoepidermoid carcinoma mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis myxedema neuropathy papillary adenocarcinoma papillary renal cell carcinoma peripheral nervous system disease polyneuropathy quadriplegia recurrent corneal erosion scoliosis sensorineural hearing loss squamous cell carcinoma syndromic X-linked intellectual disability 94 thyroid adenoma thyroid cancer thyroid gland anaplastic carcinoma thyroid gland carcinoma thyroid gland papillary carcinoma tongue squamous cell carcinoma vascular skin disease visual epilepsy
O00591	Gamma-aminobutyric acid receptor subunit pi	GABRP	Homo sapiens (human)	5	0
Q9Y5F2	Protocadherin beta-11	PCDHB11	Homo sapiens (human)	5	3
Q8N5C6	S1 RNA-binding domain-containing protein 1	SRBD1	Homo sapiens (human)	5	1
H0Y3H6	Complement C2 (Fragment)	C2	Homo sapiens (human)	5	0
Q86WK6	Amphoterin-induced protein 1	AMIGO1 ALI2 AMIGO KIAA1163	Homo sapiens (human)	5	2
Q5BJH7	Protein YIF1B	YIF1B	Homo sapiens (human)	5	1
P0DTU3	T cell receptor alpha chain MC.7.G5	TRA	Homo sapiens (human)	5	0
Q9P0K7	Ankycorbin	RAI14 KIAA1334 NORPEG	Homo sapiens (human)	5	4
Q2M3T9	Hyaluronidase-4	HYAL4	Homo sapiens (human)	5	11	oxyphilic adenoma renal oncocytoma

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