GlyCosmos Portal

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q01196	Runt-related transcription factor 1	RUNX1 AML1 CBFA2	10	2
O00487	26S proteasome non-ATPase regulatory subunit 14	PSMD14 POH1	1	2
Q9UNP9	Peptidyl-prolyl cis-trans isomerase E	PPIE CYP33	4	2
Q5T3J3	Ligand-dependent nuclear receptor-interacting factor 1	LRIF1 C1orf103 RIF1	11	2
P68371	Tubulin beta-4B chain	TUBB4B TUBB2C	7	2
Q9BV57	Acireductone dioxygenase	ADI1 MTCBP1	1	2
P46063	ATP-dependent DNA helicase Q1	RECQL RECQ1 RECQL1	2	2
Q9BVL2	Nucleoporin p58/p45	NUP58 KIAA0410 NUPL1	59	2
Q01105	Protein SET	SET	2	2
Q9Y4D8	Probable E3 ubiquitin-protein ligase HECTD4	HECTD4 C12orf51 KIAA0614	1	2
P04899	Guanine nucleotide-binding protein G(i) subunit alpha-2	GNAI2 GNAI2B	5	2
Q9H0B8	Cysteine-rich secretory protein LCCL domain-containing 2	CRISPLD2 CRISP11 LCRISP2	4	2
O43768	Alpha-endosulfine	ENSA	3	2
O75541	Zinc finger protein 821	ZNF821	1	2
Q3YEC7	Rab-like protein 6	RABL6 C9orf86 PARF	5	2
P07237	Protein disulfide-isomerase	P4HB ERBA2L PDI PDIA1 PO4DB	8	2
Q9UIJ7	GTP:AMP phosphotransferase AK3, mitochondrial	AK3 AK3L1 AK6 AKL3L	2	2
Q9H2S6	Tenomodulin	TNMD CHM1L	2	2
Q6UXI7	Vitrin	VIT	3	2
Q9NQT4	Exosome complex component RRP46	EXOSC5 CML28 RRP46	1	2
Q13454	Tumor suppressor candidate 3	TUSC3 N33	2	2	Peutz-Jeghers syndrome agnosia autosomal recessive intellectual developmental disorder 7 autosomal recessive intellectual developmental disorder bone osteosarcoma breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer central nervous system cancer cerebral degeneration childhood osteosarcoma chondrosarcoma choreatic disease chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital disorder of glycosylation depressive disorder developmental coordination disorder dysthymic disorder dystonia embryoma epilepsy esophageal cancer esophageal carcinoma esophagus squamous cell carcinoma focal epilepsy giant cell glioblastoma glioblastoma gliosarcoma hemochromatosis type 1 hemochromatosis hepatocellular carcinoma high grade glioma inflammatory bowel disease 1 inflammatory bowel disease intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia liver cancer lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma major depressive disorder melancholic depression microcephaly mixed glioma neurotic disorder nonpapillary renal cell carcinoma obsolete infantile epileptic encephalopathy obsolete melancholia osteosarcoma ovarian cancer ovarian carcinoma pancreatic cancer pancreatic carcinoma papillary renal cell carcinoma partial motor epilepsy prostate cancer prostate carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia squamous cell carcinoma stereotypic movement disorder syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 tongue squamous cell carcinoma ulcerative colitis visual epilepsy von Hippel-Lindau disease
A8MUV8	Putative zinc finger protein 727	ZNF727 ZNF727P	2	2
P40692	DNA mismatch repair protein Mlh1	MLH1 COCA2	2	2
Q8NDC0	MAPK-interacting and spindle-stabilizing protein-like	MAPK1IP1L C14orf32	10	2
Q9Y5B0	RNA polymerase II subunit A C-terminal domain phosphatase	CTDP1 FCP1	4	2

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