GlyCosmos Portal

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UniProt ID ▼	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q9UKS6	Protein kinase C and casein kinase substrate in neurons protein 3	PACSIN3	0	1
Q9UKR3	Kallikrein-13	KLK13 KLKL4	2	0
Q9UKR0	Kallikrein-12	KLK12 KLKL5	2	0
Q9UKQ9	Kallikrein-9	KLK9	3	0
Q9UKQ2	Disintegrin and metalloproteinase domain-containing protein 28	ADAM28 ADAM23 MDCL	6	3
Q9UKP6	Urotensin-2 receptor	UTS2R GPR14	2	0
Q9UKP5	A disintegrin and metalloproteinase with thrombospondin motifs 6	ADAMTS6	6	0
Q9UKP4	A disintegrin and metalloproteinase with thrombospondin motifs 7	ADAMTS7	21	4
Q9UKN8	General transcription factor 3C polypeptide 4	GTF3C4	0	1
Q9UKN7	Unconventional myosin-XV	MYO15A MYO15	0	1
Q9UKN1	Mucin-12	MUC12 MUC11	22	1
Q9UKM9	RNA-binding protein Raly	RALY HNRPCL2 P542	0	1
Q9UKM7	Endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase	MAN1B1	17	4	Hailey-Hailey disease Rafiq syndrome Rothmund-Thomson syndrome agnosia alpha 1-antitrypsin deficiency autistic disorder 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 bladder carcinoma bulimia nervosa cancer cerebral degeneration choreatic disease congenital disorder of glycosylation Ii congenital disorder of glycosylation type I congenital disorder of glycosylation cutis laxa depressive disorder developmental coordination disorder dysthymic disorder dystonia epilepsy focal epilepsy gallbladder disease hepatocellular carcinoma hyperopia intellectual disability learning disability lingual-facial-buccal dyskinesia liver cancer liver disease major depressive disorder mal de Meleda melancholic depression microcephaly neurotic disorder non-syndromic intellectual disability obsolete infantile epileptic encephalopathy obsolete melancholia oophoritis parametritis partial motor epilepsy pelvic inflammatory disease periventricular nodular heterotopia pyosalpinx restrictive dermopathy salpingitis stereotypic movement disorder syndactyly syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 urinary bladder cancer visual epilepsy
Q9UKL3	CASP8-associated protein 2	CASP8AP2 FLASH KIAA1315 RIP25	3	1
Q9UKL2	Olfactory receptor 52A1	OR52A1	1	0
Q9UKL0	REST corepressor 1	RCOR1 KIAA0071 RCOR	3	2
Q9UKK9	ADP-sugar pyrophosphatase	NUDT5 NUDIX5	0	1	breast cancer cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma embryoma nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
Q9UKK6	NTF2-related export protein 1	NXT1	0	1
Q9UKK3	Protein mono-ADP-ribosyltransferase PARP4	PARP4 ADPRTL1 KIAA0177 PARPL	4	1	Down syndrome breast cancer breast carcinoma cancer central nervous system lymphoma childhood leukemia colon cancer colonic benign neoplasm colorectal cancer embryoma esophagus squamous cell carcinoma goiter intracranial hypertension large intestine cancer leukemia lymphoma obsolete ymphosarcoma pancreatic cancer pancreatic carcinoma pseudotumor cerebri thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland disease
Q9UKJ8	Disintegrin and metalloproteinase domain-containing protein 21	ADAM21	7	0
Q9UKJ3	G patch domain-containing protein 8	GPATCH8 GPATC8 KIAA0553	2	1
Q9UKJ1	Paired immunoglobulin-like type 2 receptor alpha	PILRA	2	7
Q9UKJ0	Paired immunoglobulin-like type 2 receptor beta	PILRB FDFACT	1	0
Q9UKI9	POU domain, class 2, transcription factor 3	POU2F3 OTF11 PLA1	2	1
Q9UKI8	Serine/threonine-protein kinase tousled-like 1	TLK1 KIAA0137	2	2

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