GlyCosmos Portal

Displaying entries **1001 - 1025** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol ▲	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
P51164	Potassium-transporting ATPase subunit beta	ATP4B	7	0
P25705	ATP synthase subunit alpha, mitochondrial	ATP5F1A ATP5A ATP5A1 ATP5AL2 ATPM	7	1
P06576	ATP synthase subunit beta, mitochondrial	ATP5F1B ATP5B ATPMB ATPSB	2	1
P36542	ATP synthase subunit gamma, mitochondrial	ATP5F1C ATP5C ATP5C1 ATP5CL1	1	3
P30049	ATP synthase subunit delta, mitochondrial	ATP5F1D ATP5D	0	1
P56381	ATP synthase subunit epsilon, mitochondrial	ATP5F1E ATP5E	0	1
Q9UII2	ATPase inhibitor, mitochondrial	ATP5IF1 ATPI ATPIF1	0	1
Q06055	ATP synthase F(0) complex subunit C2, mitochondrial	ATP5MC2 ATP5G2	0	1
P48201	ATP synthase F(0) complex subunit C3, mitochondrial	ATP5MC3 ATP5G3	0	1
P56385	ATP synthase subunit e, mitochondrial	ATP5ME ATP5I ATP5K	1	1
P56134	ATP synthase subunit f, mitochondrial	ATP5MF ATP5J2 ATP5JL	0	1
Q96IX5	ATP synthase membrane subunit K, mitochondrial	ATP5MK ATP5MD DAPIT HCVFTP2 USMG5	0	1
P24539	ATP synthase F(0) complex subunit B1, mitochondrial	ATP5PB ATP5F1	0	1
O75947	ATP synthase subunit d, mitochondrial	ATP5PD ATP5H	0	1
P48047	ATP synthase subunit O, mitochondrial	ATP5PO ATP5O ATPO	0	1
Q15904	V-type proton ATPase subunit S1	ATP6AP1 ATP6IP1 ATP6S1 VATPS1 XAP3	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
A0A7I2YQA5	ATPase H+ transporting accessory protein 1	ATP6AP1	1	0
A0A7I2V3T8	ATPase H+ transporting accessory protein 1	ATP6AP1	1	0
A6QRJ1	ATPase H+ transporting accessory protein 1 (Fragment)	ATP6AP1	1	0
Q93050	V-type proton ATPase 116 kDa subunit a 1	ATP6V0A1 ATP6N1 ATP6N1A VPP1	1	4
Q9Y487	V-type proton ATPase 116 kDa subunit a 2	ATP6V0A2	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
Q9HBG4	V-type proton ATPase 116 kDa subunit a 4	ATP6V0A4 ATP6N1B ATP6N2	1	0
P27449	V-type proton ATPase 16 kDa proteolipid subunit c	ATP6V0C ATP6C ATP6L ATPL	3	1
P61421	V-type proton ATPase subunit d 1	ATP6V0D1 ATP6D VPATPD	0	1
O15342	V-type proton ATPase subunit e 1	ATP6V0E1 ATP6H ATP6V0E	2	8

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