GlyCosmos Portal

Displaying entries **5326 - 5350** of **18496** in total

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UniProt ID	Protein Name ▼	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q6UVM3	Potassium channel subfamily T member 2	KCNT2 SLICK	1	0
Q5JUK3	Potassium channel subfamily T member 1	KCNT1 KIAA1422	2	0
Q9NPC2	Potassium channel subfamily K member 9	KCNK9 TASK3	1	0
Q9Y2U2	Potassium channel subfamily K member 7	KCNK7	1	0
Q9Y257	Potassium channel subfamily K member 6	KCNK6 TOSS TWIK2	2	0
O95279	Potassium channel subfamily K member 5	KCNK5 TASK2	1	1
Q9NYG8	Potassium channel subfamily K member 4	KCNK4 TRAAK	2	0
O14649	Potassium channel subfamily K member 3	KCNK3 TASK TASK1	1	0
O95069	Potassium channel subfamily K member 2	KCNK2 TREK TREK1	4	1
Q7Z418	Potassium channel subfamily K member 18	KCNK18 TRESK TRIK	1	0
Q96T54	Potassium channel subfamily K member 17	KCNK17 TALK2 TASK4	2	0
Q9HB14	Potassium channel subfamily K member 13	KCNK13	2	0
Q9HB15	Potassium channel subfamily K member 12	KCNK12	1	0
P57789	Potassium channel subfamily K member 10	KCNK10 TREK2	4	1
O00180	Potassium channel subfamily K member 1	KCNK1 HOHO1 KCNO1 TWIK1	1	0
B2RCT9	Potassium channel subfamily K member	KCNK17	1	0
B2RDS2	Potassium channel subfamily K member	KCNK6	1	0
Q9HCN3	Post-GPI attachment to proteins factor 6	PGAP6 TMEM6 TMEM8 TMEM8A	6	5
Q9BRR3	Post-GPI attachment to proteins factor 4	PGAP4 C9orf125 TMEM246	1	0
Q96FM1	Post-GPI attachment to proteins factor 3	PGAP3 CAB2 PERLD1	1	7	Cogan syndrome Crohn's colitis Crohn's disease Hirschsprung's disease Marfan syndrome Unverricht-Lundborg syndrome allergic asthma asthma bipolar disorder blepharospasm breast cancer breast carcinoma bruxism capillary disease congenital diaphragmatic hernia congenital disorder of glycosylation craniosynostosis diffuse interstitial keratitis early myoclonic encephalopathy epilepsy esotropia focal hand dystonia hereditary hemorrhagic telangiectasia hydronephrosis hyperopia inflammatory bowel disease 1 inflammatory bowel disease intellectual disability intrinsic asthma isolated cleft palate learning disability lingual-facial-buccal dyskinesia monocular esotropia movement disease oligohydramnios scoliosis situs inversus stomach cancer stomach carcinoma syndromic X-linked intellectual disability 94 telangiectasis tuberous sclerosis ulcerative colitis visual epilepsy
P08397	Porphobilinogen deaminase	HMBS PBGD UPS	0	1
Q8N131	Porimin	TMEM123 KCT3	13	3
Q9HBV1	Popeye domain-containing protein 3	POPDC3 POP3	1	0
Q9HBU9	Popeye domain-containing protein 2	POPDC2 POP2	1	1
P18054	Polyunsaturated fatty acid lipoxygenase ALOX12	ALOX12 12LO LOG12	1	1	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 Becker muscular dystrophy Duchenne muscular dystrophy Pick's disease Reye syndrome actinic keratosis acute myeloid leukemia acute myocardial infarction adenocarcinoma adenoma adult lymphoma amyloidosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bacterial sepsis benign mesothelioma bipolar disorder bone marrow cancer breast cancer breast carcinoma cancer cardiovascular system disease central nervous system lymphoma cerebral degeneration cerebral infarction cerebrovascular disease childhood lymphoma chromophobe renal cell carcinoma clear cell renal cell carcinoma colitis collecting duct carcinoma colorectal cancer colorectal carcinoma cone-rod dystrophy 2 cone-rod dystrophy congenital toxoplasmosis congestive heart failure coronary artery disease coronary thrombosis cribriform carcinoma diabetes mellitus diabetic ketoacidosis distal myopathy embryoma endomyocardial fibrosis esophagus squamous cell carcinoma essential hypertension facioscapulohumeral muscular dystrophy follicular adenoma gastroenteritis glomerulonephritis granular cell carcinoma heart disease hepatocellular carcinoma hypertension ileitis ileocolitis juvenile rheumatoid arthritis kidney disease kidney hypertrophy large intestine cancer leech infestation limb-girdle muscular dystrophy liver cancer lymphoma malignant mesothelioma melanoma microcystic adenoma muscular dystrophy myeloproliferative neoplasm myiasis myocardial infarction nephritis nephrosis neuroblastoma neurodegenerative disease neuropathy nodular prostate nonpapillary renal cell carcinoma obesity obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete type 1 diabetes mellitus 9 obsolete ymphosarcoma oculopharyngeal muscular dystrophy osteoporosis ovarian cancer ovarian carcinoma papillary adenoma papillary renal cell carcinoma parapsoriasis peripheral nervous system disease pneumonia post-traumatic stress disorder prostate cancer prostate carcinoma prostatic adenoma psoriasis pustulosis of palm and sole pyoureter rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma retinal disease retinitis rheumatoid arthritis sarcomatoid renal cell carcinoma schizophrenia seborrheic keratosis silent myocardial infarction skin benign neoplasm skin cancer skin disease skin melanoma squamous cell carcinoma steatotic liver disease stomach cancer stomach carcinoma testicular cancer thyroid adenoma thyroid cancer thyroid gland carcinoma tongue squamous cell carcinoma toxoplasmosis tuberculosis tubular adenocarcinoma type 1 diabetes mellitus 10 type 1 diabetes mellitus 11 type 1 diabetes mellitus 12 type 1 diabetes mellitus 13 type 1 diabetes mellitus 15 type 1 diabetes mellitus 17 type 1 diabetes mellitus 18 type 1 diabetes mellitus 19 type 1 diabetes mellitus 20 type 1 diabetes mellitus 21 type 1 diabetes mellitus 22 type 1 diabetes mellitus 23 type 1 diabetes mellitus 24 type 1 diabetes mellitus 2 type 1 diabetes mellitus 3 type 1 diabetes mellitus 4 type 1 diabetes mellitus 5 type 1 diabetes mellitus 6 type 1 diabetes mellitus 7 type 1 diabetes mellitus 8 type 1 diabetes mellitus type 2 diabetes mellitus urinary bladder cancer vitelliform macular dystrophy vitiligo

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