GlyCosmos Portal

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Displaying entries **122051 - 122075** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol ▼	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P21281	V-type proton ATPase subunit B, brain isoform	ATP6V1B2 ATP6B2 VPP3	Homo sapiens (human)	0	1
P38606	V-type proton ATPase catalytic subunit A	ATP6V1A ATP6A1 ATP6V1A1 VPP2	Homo sapiens (human)	5	1	American histoplasmosis Dandy-Walker syndrome Joubert syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Unverricht-Lundborg syndrome achondroplasia agnosia angioma serpiginosum anodontia aspergillosis atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect attention deficit hyperactivity disorder autistic disorder autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID black piedra blepharophimosis blepharospasm brain disease capillary hemangioma cardiomyopathy cataract cavernous hemangioma cerebral degeneration clubfoot coccidioidomycosis coloboma colorectal cancer colorectal carcinoma complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital nystagmus congenital ptosis congestive heart failure cortical dysplasia-focal epilepsy syndrome cryptorchidism cutis laxa dementia dental caries dentin caries developmental coordination disorder dissociated nystagmus dystonia early myoclonic encephalopathy endomyocardial fibrosis entropion epilepsy esophagitis familial hypertrophic cardiomyopathy focal hand dystonia gastroesophageal reflux disease histoplasmosis hydranencephaly hyperopia hypertrophic cardiomyopathy hypertropia inguinal hernia intellectual disability large intestine cancer learning disability lingual-facial-buccal dyskinesia lipoatrophic diabetes mellitus lipodystrophy lissencephaly mechanical strabismus microcephaly obsolete infantile epileptic encephalopathy ophthalmoplegia optic atrophy patent foramen ovale pathologic nystagmus peptic esophagitis placental insufficiency pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 ptosis retinal degeneration schizophrenia septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly spontaneous ocular nystagmus sporotrichosis status epilepticus stomach cancer stomach carcinoma strabismus superficial mycosis syndromic X-linked intellectual disability Najm type tooth agenesis visual epilepsy white piedra
Q2KIB5	V-type proton ATPase subunit e 2	ATP6V0E2	Bos taurus (cattle)	1	0
Q8NHE4	V-type proton ATPase subunit e 2	ATP6V0E2 ATP6V0E2L C7orf32	Homo sapiens (human)	2	3
Q5RAV0	V-type proton ATPase subunit e 1	ATP6V0E1 ATP6V0E	Pongo abelii (Sumatran orangutan)	1	0
O15342	V-type proton ATPase subunit e 1	ATP6V0E1 ATP6H ATP6V0E	Homo sapiens (human)	2	8
Q9BDP4	V-type proton ATPase subunit e 1	ATP6V0E1 ATP6H ATP6V0E	Canis lupus familiaris (dog)	1	0
P81103	V-type proton ATPase subunit e 1	ATP6V0E1 ATP6H ATP6V0E	Bos taurus (cattle)	1	0
P61421	V-type proton ATPase subunit d 1	ATP6V0D1 ATP6D VPATPD	Homo sapiens (human)	0	1
P27449	V-type proton ATPase 16 kDa proteolipid subunit c	ATP6V0C ATP6C ATP6L ATPL	Homo sapiens (human)	3	1
Q9HBG4	V-type proton ATPase 116 kDa subunit a 4	ATP6V0A4 ATP6N1B ATP6N2	Homo sapiens (human)	1	0
Q9Y487	V-type proton ATPase 116 kDa subunit a 2	ATP6V0A2	Homo sapiens (human)	5	7	Crohn's colitis Crohn's disease Dandy-Walker syndrome Ehlers-Danlos syndrome Hailey-Hailey disease Joubert syndrome Laron syndrome Miller-Dieker lissencephaly syndrome Rothmund-Thomson syndrome achondroplasia agnosia alopecia aortic valve disease 1 aortic valve disease 2 aortic valve stenosis arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB autosomal recessive osteopetrosis 7 bacterial sepsis bicuspid aortic valve disease bone disease breast cancer breast carcinoma cancer cartilage disease clubfoot complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital disorder of glycosylation Il congenital disorder of glycosylation type I congenital disorder of glycosylation congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 connective tissue disease coronary artery disease cortical dysplasia-focal epilepsy syndrome cryptococcosis cryptorchidism cutis laxa dementia dental caries dentin caries developmental coordination disorder diabetic cataract diabetic retinopathy encephalitis encephalomyelitis epilepsy essential hypertension generalized atherosclerosis geroderma osteodysplasticum giant cell glioblastoma glioblastoma gliosarcoma high grade glioma hydranencephaly hypertension hypertropia inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intracranial aneurysm learning disability lipoatrophic diabetes mellitus lipodystrophy lissencephaly lung disease mal de Meleda male infertility mechanical strabismus microcephaly mixed glioma myelitis myopia omphalocele ophthalmoplegia osteogenesis imperfecta osteopetrosis osteosclerosis placental insufficiency platelet-type bleeding disorder 11 platelet-type bleeding disorder 3 platelet-type bleeding disorder 8 platelet-type bleeding disorder 9 pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 pulmonary emphysema renal tubular acidosis restrictive dermopathy scoliosis septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly status epilepticus strabismus syndromic X-linked intellectual disability Najm type ulcerative colitis umbilical hernia visual epilepsy von Willebrand's disease
Q93050	V-type proton ATPase 116 kDa subunit a 1	ATP6V0A1 ATP6N1 ATP6N1A VPP1	Homo sapiens (human)	1	4
A0A7I2YQA5	ATPase H+ transporting accessory protein 1	ATP6AP1	Homo sapiens (human)	1	0
A0A7I2V3T8	ATPase H+ transporting accessory protein 1	ATP6AP1	Homo sapiens (human)	1	0
A6QRJ1	ATPase H+ transporting accessory protein 1 (Fragment)	ATP6AP1	Homo sapiens (human)	1	0
P40682	V-type proton ATPase subunit S1	ATP6AP1 ATP6IP1 ATP6S1	Bos taurus (cattle)	8	0
Q15904	V-type proton ATPase subunit S1	ATP6AP1 ATP6IP1 ATP6S1 VATPS1 XAP3	Homo sapiens (human)	10	53	Hailey-Hailey disease Rothmund-Thomson syndrome autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB cancer congenital disorder of glycosylation cutis laxa exocrine pancreatic insufficiency follicular lymphoma gallbladder disease hyperopia leukopenia liver disease mal de Meleda restrictive dermopathy steatotic liver disease tuberculosis
P13621	ATP synthase subunit O, mitochondrial	ATP5PO ATP5O	Bos taurus (cattle)	0	1
P48047	ATP synthase subunit O, mitochondrial	ATP5PO ATP5O ATPO	Homo sapiens (human)	0	1
P13620	ATP synthase subunit d, mitochondrial	ATP5PD ATP5H	Bos taurus (cattle)	0	1
O75947	ATP synthase subunit d, mitochondrial	ATP5PD ATP5H	Homo sapiens (human)	0	1
P24539	ATP synthase F(0) complex subunit B1, mitochondrial	ATP5PB ATP5F1	Homo sapiens (human)	0	1
P13619	ATP synthase F(0) complex subunit B1, mitochondrial	ATP5PB ATP5F ATP5F1	Bos taurus (cattle)	0	1
Q96IX5	ATP synthase membrane subunit K, mitochondrial	ATP5MK ATP5MD DAPIT HCVFTP2 USMG5	Homo sapiens (human)	0	1

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