GlyCosmos Portal

Displaying entries **12251 - 12275** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▲	No. of GlyTouCan IDs	Disease Ontology
Q9UHP7	C-type lectin domain family 2 member D	CLEC2D CLAX LLT1 OCIL	2	0
D3W0D1	Killer cell lectin-like receptor subfamily F member 2	KLRF2	2	0
Q96EE4	Coiled-coil domain-containing protein 126	CCDC126	2	1
H9KV48	Serpin family G member 1	SERPING1	2	0
Q8IYD1	Eukaryotic peptide chain release factor GTP-binding subunit ERF3B	GSPT2 ERF3B	2	1
Q6DN72	Fc receptor-like protein 6	FCRL6 FCRH6	2	0
Q0ZGT2	Nexilin	NEXN	2	3
A0A7I2V5Q1	Cathepsin F	CTSF	2	0
Q53GL7	Protein mono-ADP-ribosyltransferase PARP10	PARP10	2	1	ataxia telangiectasia bipolar I disorder bipolar disorder hepatocellular carcinoma liver cancer neurodegenerative disease pancreatic cancer pancreatic carcinoma
Q8IWE2	Protein NOXP20	FAM114A1 NOXP20	2	1
P46063	ATP-dependent DNA helicase Q1	RECQL RECQ1 RECQL1	2	2
Q01105	Protein SET	SET	2	2
Q12965	Unconventional myosin-Ie	MYO1E MYO1C	2	6
Q86UW1	Organic solute transporter subunit alpha	SLC51A OSTA	2	1
Q16799	Reticulon-1	RTN1 NSP	2	1
Q9Y5G6	Protocadherin gamma-A7	PCDHGA7	2	1
Q9UIJ7	GTP:AMP phosphotransferase AK3, mitochondrial	AK3 AK3L1 AK6 AKL3L	2	2
P32418	Sodium/calcium exchanger 1	SLC8A1 CNC NCX1	2	0
B8YAC7	MHC class II antigen (Fragment)	HLA-DRB3	2	0
Q9H2S6	Tenomodulin	TNMD CHM1L	2	2
Q13491	Neuronal membrane glycoprotein M6-b	GPM6B M6B	2	0
P24752	Acetyl-CoA acetyltransferase, mitochondrial	ACAT1 ACAT MAT	2	7	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Bannayan-Riley-Ruvalcaba syndrome Cowden syndrome Crohn's colitis Crohn's disease Pick's disease Reye syndrome adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenal gland hyperfunction adrenocortical carcinoma adult hepatocellular carcinoma age related macular degeneration agnosia alopecia amyloidosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ataxia telangiectasia atherosclerosis bacterial sepsis beta-ketothiolase deficiency bronchus cancer bronchus carcinoma cancer cardiovascular system disease central nervous system cancer cerebral degeneration chancroid childhood hepatocellular carcinoma chromophobe renal cell carcinoma chronic kidney disease clear cell renal cell carcinoma colitis collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congestive heart failure coronary artery disease cribriform carcinoma cystathioninuria degeneration of macula and posterior pole developmental coordination disorder diabetes mellitus diarrhea disease of metabolism dry eye syndrome embryoma epilepsy essential hypertension familial hyperlipidemia familial nephrotic syndrome focal epilepsy gastroenteritis giant cell glioblastoma glioblastoma gliosarcoma granular cell carcinoma heart disease hepatitis C hepatocellular carcinoma high grade glioma hyperglycemia hypertension hyperuricemia hypoglycemia ileitis ileocolitis inflammatory bowel disease 1 inflammatory bowel disease inherited metabolic disorder intellectual disability kwashiorkor lactic acidosis large intestine cancer learning disability leptospirosis lipoid nephrosis liver cancer liver cirrhosis lung benign neoplasm lung cancer lung carcinoma lymphogranuloma venereum macular degeneration malignant teratoma marasmus mature teratoma mixed glioma necrotizing ulcerative gingivitis nephrotic syndrome neuroblastoma nonpapillary renal cell carcinoma nutmeg liver nutrition disease obsolete Cushing's syndrome papillary renal cell carcinoma partial motor epilepsy pneumocystosis primary hyperaldosteronism prostate cancer prostate carcinoma protein-energy malnutrition rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma steatotic liver disease syndromic X-linked intellectual disability 94 teratoma thrombocytosis trypanosomiasis tubular adenocarcinoma type 2 diabetes mellitus tyrosinemia type I tyrosinemia ulcerative colitis urea cycle disorder uterine cancer uterine corpus cancer visual epilepsy xanthomatosis xerophthalmia yaws
P22466	Galanin peptides	GAL GAL1 GALN GLNN	2	1
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
Q8IXJ9	Polycomb group protein ASXL1	ASXL1 KIAA0978	2	1

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