GlyCosmos Portal

Displaying entries **1901 - 1925** of **18496** in total

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UniProt ID	Protein Name	Gene Symbol	No. of Glycosylation Sites ▼	No. of GlyTouCan IDs	Disease Ontology
O75473	Leucine-rich repeat-containing G-protein coupled receptor 5	LGR5 GPR49 GPR67	6	0
Q9H7S9	Zinc finger protein 703	ZNF703 ZEPPO1 ZPO1	6	1
Q12815	Tastin	TROAP	6	1
A8K2U0	Alpha-2-macroglobulin-like protein 1	A2ML1 CPAMD9	6	4
Q96S16	JmjC domain-containing protein 8	JMJD8 C16orf20	6	2
P36955	Pigment epithelium-derived factor	SERPINF1 PEDF	6	57
Q96MU8	Kremen protein 1	KREMEN1 KREMEN KRM1	6	0
A8MWY0	Endosome/lysosome-associated apoptosis and autophagy regulator family member 2	ELAPOR2 EIG121L KIAA1324L	6	3
Q9Y4B6	DDB1- and CUL4-associated factor 1	DCAF1 KIAA0800 RIP VPRBP	6	3
Q9NZN1	Interleukin-1 receptor accessory protein-like 1	IL1RAPL1 OPHN4	6	0	B-cell lymphoma Bell's palsy Coffin-Lowry syndrome Klinefelter syndrome Marfan syndrome Meckel's diverticulum Patau syndrome X-linked adrenal hypoplasia congenita allergic asthma asthma attention deficit hyperactivity disorder autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome brain cancer breast cancer breast carcinoma cancer cardiovascular system disease chromosome Xp21 deletion syndrome clubfoot diffuse large B-cell lymphoma embryoma facial nerve disease facial paralysis heart disease hepatocellular carcinoma immune system disease intellectual disability intrinsic asthma learning disability liver cancer melanoma non-syndromic X-linked intellectual disability obesity obsolete ymphosarcoma placental insufficiency pyloric stenosis rheumatoid arthritis situs inversus skin melanoma syndromic X-linked intellectual disability 94 tuberous sclerosis visual epilepsy vitiligo
P15924	Desmoplakin	DSP	6	3
Q70UQ0	Inhibitor of nuclear factor kappa-B kinase-interacting protein	IKBIP IKIP	6	31
C9JYY6	Neuronal cell adhesion molecule	NRCAM	6	0
Q9NRM6	Interleukin-17 receptor B	IL17RB CRL4 EVI27 IL17BR	6	8
Q5FYB0	Arylsulfatase J	ARSJ	6	0
Q8IZF5	Adhesion G-protein coupled receptor F3	ADGRF3 GPR113 PGR23	6	1
Q6UB99	Ankyrin repeat domain-containing protein 11	ANKRD11 ANCO1	6	1
Q9NQ25	SLAM family member 7	SLAMF7 CS1	6	1
O75694	Nuclear pore complex protein Nup155	NUP155 KIAA0791	6	1
Q6NUS6	Tectonic-3	TCTN3 C10orf61 TECT3	6	11
Q6UXV0	GDNF family receptor alpha-like	GFRAL C6orf144	6	0
Q9UJ99	Cadherin-22	CDH22 C20orf25	6	1
Q3V5L5	Alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B	MGAT5B KIAA2008	6	5	brain cancer cancer chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma hepatocellular carcinoma liver cancer neuroblastoma nonpapillary renal cell carcinoma papillary renal cell carcinoma polycystic ovary syndrome renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
Q7LGC8	Carbohydrate sulfotransferase 3	CHST3	6	4	Bannayan-Riley-Ruvalcaba syndrome Bartter disease Conn's syndrome Cowden syndrome Desbuquois dysplasia Hailey-Hailey disease Laron syndrome Larsen syndrome Larsen-like syndrome B3GAT3 type Ollier disease Rothmund-Thomson syndrome SOST-related sclerosing bone dysplasia Schwartz-Jampel syndrome 1 Silverman-Handmaker type dyssegmental dysplasia Sjogren's syndrome Waterhouse-Friderichsen syndrome X-linked spondyloepiphyseal dysplasia tarda achondroplasia acute promyelocytic leukemia adenocarcinoma adenoma adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenocortical carcinoma adrenoleukodystrophy adult fibrosarcoma agnosia alcoholic hepatitis alcoholic liver cirrhosis amblyopia aortic valve disease 1 aortic valve disease 2 aortic valve insufficiency aortic valve stenosis apparent mineralocorticoid excess syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atopic dermatitis 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 atrophy of testis autoimmune hepatitis 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 bicuspid aortic valve disease blastomycosis breast cancer breast carcinoma buphthalmos cancer cardiomyopathy cardiovascular system disease choriocarcinoma cleft palate cleidocranial dysplasia clubfoot communicating hydrocephalus congenital adrenal hyperplasia coronary artery disease craniosynostosis cutis laxa cystadenoma dermatitis developmental coordination disorder diabetes mellitus diabetic ketoacidosis diastrophic dysplasia embryoma endometrial adenocarcinoma endometrial cancer endometrial carcinoma endometrial hyperplasia endometriosis of uterus endometriosis endomyocardial fibrosis enterocele esotropia essential hypertension fibrosarcoma follicular adenoma heart disease hepatitis hereditary multiple exostoses humeroradial synostosis hydrocephalus hydrophthalmos hyperopia hypertension hypertrophic cardiomyopathy hypogonadotropic hypogonadism 23 with or without anosmia inclusion body myositis intrahepatic cholestasis isolated cleft palate juvenile glaucoma keratoconjunctivitis sicca leiomyoma liver cirrhosis lung small cell carcinoma mal de Meleda microcystic adenoma mitral valve insufficiency mitral valve prolapse mitral valve stenosis monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia myofibroma neurogenic arthropathy obesity obsolete type 1 diabetes mellitus 9 obstructive hydrocephalus osteochondrodysplasia osteoporosis ovarian cancer ovarian carcinoma ovarian hyperstimulation syndrome papillary adenoma paracoccidioidomycosis patent foramen ovale placenta cancer polycystic ovary syndrome postural orthostatic tachycardia syndrome primary hyperaldosteronism primary pulmonary hypertension progressive familial intrahepatic cholestasis progressive pseudorheumatoid arthropathy of childhood pulmonary valve stenosis radioulnar synostosis restrictive dermopathy rheumatoid arthritis schizophrenia scoliosis senile degeneration of brain sensorineural hearing loss spondyloepiphyseal dysplasia congenita spondyloepiphyseal dysplasia with congenital joint dislocations strabismic amblyopia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tricuspid valve insufficiency tricuspid valve stenosis 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 uterine corpus cancer uterine fibroid varicose veins ventricular septal defect
O95803	Bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 3	NDST3 HSST3	6	0	Balo concentric sclerosis adrenoleukodystrophy anxiety disorder central nervous system disease depressive disorder generalized anxiety disorder major depressive disorder melancholic depression narcolepsy neurotic disorder obsolete melancholia schizophrenia

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