GlyCosmos Portal

Source	Last Updated
GlyConnect	March 24, 2025
GlycoProtDB	December 4, 2018
GlyGen	October 30, 2024
The O-GlcNAc Database	January 30, 2025
UniProt	February 20, 2025

Displaying entries **201 - 225** of **139028** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology ▲
Q8TAM2	Tetratricopeptide repeat protein 8	BBS8 TTC8	Homo sapiens (human)	1	1	Bardet-Biedl syndrome 8 Bardet-Biedl syndrome retinitis pigmentosa 51
Q3SYG4	Protein PTHB1	BBS9 PTHB1	Homo sapiens (human)	2	1	Bardet-Biedl syndrome 9 Bardet-Biedl syndrome craniosynostosis primary ovarian insufficiency
P03956	Interstitial collagenase	CLG MMP1	Homo sapiens (human)	2	48	Barrett's esophagus abdominal aortic aneurysm aortic valve stenosis arteriosclerosis atherosclerosis atrial fibrillation breast cancer carotid artery disease carotid stenosis cervical cancer congestive heart failure coronary artery disease dilated cardiomyopathy end stage renal disease epidermolysis bullosa dystrophica esophagus adenocarcinoma hypertension hypertrophic cardiomyopathy intermediate coronary syndrome localized scleroderma lung cancer myocardial infarction obstructive lung disease ocular hypertension ovarian cancer primary open angle glaucoma pulmonary emphysema renal cell carcinoma renal fibrosis skin melanoma thoracic aortic aneurysm thrombosis urinary bladder cancer varicose veins
P39900	Macrophage metalloelastase	HME MMP12	Homo sapiens (human)	2	0	Barrett's esophagus abdominal aortic aneurysm arteriosclerosis coronary aneurysm coronary artery disease esophagus adenocarcinoma multiple sclerosis
P21757	Macrophage scavenger receptor types I and II	MSR1 SCARA1	Homo sapiens (human)	7	10	Barrett's esophagus arteriosclerosis prostate cancer
Q9H334	Forkhead box protein P1	FOXP1 HSPC215	Homo sapiens (human)	10	2	Barrett's esophagus congenital heart disease esophagus adenocarcinoma intellectual disability-severe speech delay-mild dysmorphism syndrome peritonitis schizophrenia
P97698	Protein smoothened	Smo Smoh	Rattus norvegicus (Norway rat)	3	0	Barrett's esophagus esophagus adenocarcinoma liver cirrhosis middle cerebral artery infarction
Q9NPZ5	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 2	B3GAT2 GLCATS KIAA1963	Homo sapiens (human)	2	0	Barrett's esophagus schizophrenia
Q96CG8	Collagen triple helix repeat-containing protein 1	CTHRC1 UNQ762/PRO1550	Homo sapiens (human)	2	0	Barrett's esophagus
Q07646	Mesoderm-specific transcript protein	121a Mest Peg1	Mus musculus (house mouse)	1	0	Barth syndrome
Q13621	Solute carrier family 12 member 1	NKCC2 SLC12A1	Homo sapiens (human)	3	0	Bartter disease type 1 Bartter disease
P55014	Solute carrier family 12 member 1	Nkcc2 Slc12a1	Mus musculus (house mouse)	2	0	Bartter disease type 1
P48048	ATP-sensitive inward rectifier potassium channel 1	KCNJ1 ROMK1	Homo sapiens (human)	1	0	Bartter disease type 2
O88335	ATP-sensitive inward rectifier potassium channel 1	Kcnj1	Mus musculus (house mouse)	1	0	Bartter disease type 2
P51801	Chloride channel protein ClC-Kb	CLCNKB	Homo sapiens (human)	1	0	Bartter disease type 3 Bartter disease type 4b Gitelman syndrome hypertension
Q9WUB6	Chloride channel protein ClC-Kb	Clckb Clcnk1l Clcnkb	Mus musculus (house mouse)	1	0	Bartter disease type 3 Bartter disease
Q9UNF1	Melanoma-associated antigen D2	BCG1 MAGED2	Homo sapiens (human)	9	2	Bartter disease type 5
A1YYN3	FGFR2	Fgfr2	Mus musculus (house mouse)	3	0	Beare-Stevenson cutis gyrata syndrome Crouzon syndrome Pfeiffer syndrome acrocephalosyndactylia intestinal atresia
P11532	Dystrophin	DMD	Homo sapiens (human)	6	3	Becker muscular dystrophy Duchenne muscular dystrophy X-linked dilated cardiomyopathy cognitive disorder dilated cardiomyopathy intellectual disability
P11531	Dystrophin	Dmd	Mus musculus (house mouse)	5	4	Becker muscular dystrophy Duchenne muscular dystrophy
Q62261	Spectrin beta chain, non-erythrocytic 1	Elf Spnb-2 Spnb2 Sptb2 Sptbn1	Mus musculus (house mouse)	7	3	Beckwith-Wiedemann syndrome
P04275	von Willebrand factor	F8VWF VWF	Homo sapiens (human)	30	203	Behcet's disease Bernard-Soulier syndrome atrial fibrillation end stage renal disease essential thrombocythemia pulmonary hypertension von Willebrand's disease 1 von Willebrand's disease 2 von Willebrand's disease 3 von Willebrand's disease
Q9HC29	Nucleotide-binding oligomerization domain-containing protein 2	CARD15 NOD2	Homo sapiens (human)	1	0	Behcet's disease Blau syndrome Crohn's disease PFAPA syndrome asthma autoimmune disease breast cancer bronchiolitis obliterans chronic obstructive pulmonary disease colorectal adenocarcinoma coronary artery disease familial Mediterranean fever gastritis gastrointestinal carcinoma graft-versus-host disease intestinal disease larynx cancer leprosy lung cancer meningococcal meningitis ovarian cancer pulmonary sarcoidosis pulmonary tuberculosis relapsing-remitting multiple sclerosis rhinitis systemic lupus erythematosus
P49279	Natural resistance-associated macrophage protein 1	LSH NRAMP NRAMP1 SLC11A1	Homo sapiens (human)	2	0	Behcet's disease Buruli ulcer disease Crohn's disease cutaneous leishmaniasis inflammatory bowel disease juvenile rheumatoid arthritis leprosy lymphoproliferative syndrome multiple sclerosis pulmonary tuberculosis rheumatoid arthritis sarcoidosis systemic lupus erythematosus systemic scleroderma tuberculosis type 1 diabetes mellitus ulcerative colitis urinary bladder cancer visceral leishmaniasis
P12821	Angiotensin-converting enzyme	ACE DCP DCP1	Homo sapiens (human)	23	113	Behcet's disease COVID-19 Coronavirus infectious disease Fabry disease IgA glomerulonephritis IgA vasculitis allergic disease anemia ankylosing spondylitis aspiration pneumonia asthma atrial fibrillation breast cancer cerebral infarction chronic obstructive pulmonary disease coronary artery disease diabetic retinopathy diastolic heart failure end stage renal disease familial Mediterranean fever gallbladder adenocarcinoma heart valve disease hepatitis A hepatocellular carcinoma hypertension leukemia liver cirrhosis lung cancer mitral valve disease mitral valve prolapse multiple myeloma myocardial infarction nephritis non-arteritic anterior ischemic optic neuropathy obstructive sleep apnea pneumonia polycythemia pre-eclampsia proteinuria sarcoidosis stomach cancer subacute sclerosing panencephalitis toxic shock syndrome type 1 diabetes mellitus type 2 diabetes mellitus

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