GlyCosmos Portal

Displaying entries **1326 - 1350** of **18496** in total

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UniProt ID	Protein Name ▲	Gene Symbol	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
Q075Z2	Binder of sperm protein homolog 1	BSPH1	1	0
Q6QNY0	Biogenesis of lysosome-related organelles complex 1 subunit 3	BLOC1S3 BLOS3	0	1
Q8TDH9	Biogenesis of lysosome-related organelles complex 1 subunit 5	BLOC1S5 MUTED	0	1
Q96IK1	Biorientation of chromosomes in cell division protein 1	BOD1 FAM44B	1	1
Q8NFC6	Biorientation of chromosomes in cell division protein 1-like 1	BOD1L1 BOD1L FAM44A KIAA1327	6	1
P43251	Biotinidase	BTD	6	63
A0A5F9ZH15	Biotinidase	BTD	3	0
A0A5F9ZHR1	Biotinidase	BTD	1	0
A0A5F9ZH97	Biotinidase	BTD	1	0
A0A5F9ZH57	Biotinidase	BTD	1	0
A0A5F9ZHE9	Biotinidase	BTD	1	0
A0A2R8Y5J9	Biotinidase	BTD	1	0
A0A5F9ZH80	Biotinidase	BTD	2	0
A0A5F9ZHF5	Biotinidase	BTD	1	0
C9JSN9	Biotinidase (Fragment)	BTD	2	0
Q9Y6X5	Bis(5'-adenosyl)-triphosphatase ENPP4	ENPP4 KIAA0879 NPP4	9	21
O75503	Bis(monoacylglycero)phosphate synthase CLN5	CLN5 BMPS	8	66	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 Lafora disease MERRF syndrome Pick's disease Reye syndrome Unverricht-Lundborg syndrome agnosia blepharospasm blindness brain disease cerebellar ataxia cerebellar disease cerebral degeneration early myoclonic encephalopathy epilepsy eye disease focal hand dystonia intellectual disability learning disability neurodegenerative disease neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis retinal degeneration visual epilepsy
A0A1B0GWI2	Bis(monoacylglycero)phosphate synthase CLN5 (Fragment)	CLN5	4	0
P07738	Bisphosphoglycerate mutase	BPGM	6	0	acquired polycythemia cholecystitis cholecystolithiasis choledocholithiasis cholelithiasis erythropoietin polycythemia familial erythrocytosis 2 normocytic anemia polycythemia vera polycythemia stress polycythemia
Q13867	Bleomycin hydrolase	BLMH	0	1
Q8NE79	Blood vessel epicardial substance	BVES POP1 POPDC1	2	0
Q9Y3E2	BolA-like protein 1	BOLA1	1	2
Q9H3K6	BolA-like protein 2	BOLA2 BOLA2B BOLA2A	0	1
P32247	Bombesin receptor subtype-3	BRS3	2	0
P13727	Bone marrow proteoglycan	PRG2 MBP	7	6	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 Duchenne muscular dystrophy Ehlers-Danlos syndrome spondylodysplastic type 2 Pick's disease Reye syndrome allergic asthma asthma autosomal dominant Emery-Dreifuss muscular dystrophy 2 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 breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer cerebral degeneration cholera colorectal cancer colorectal carcinoma congenital muscular dystrophy dermatophytosis dilated cardiomyopathy 1A dilated cardiomyopathy distal myopathy embryoma endometrial cancer endometrial carcinoma eosinophilic esophagitis facioscapulohumeral muscular dystrophy fungal infectious disease intrinsic asthma large intestine cancer limb-girdle muscular dystrophy lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma muscular dystrophy myelofibrosis myofibrillar myopathy 1 myofibrillar myopathy 3 nodular prostate 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 oculopharyngeal muscular dystrophy prostate cancer prostate carcinoma prostatic adenoma rippling muscle disease 2 uterine corpus cancer

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