GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
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The O-GlcNAc Database	June 3, 2024
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Displaying entries **3026 - 3050** 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
Q2TAA5	GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase	ALG11 GT8	Homo sapiens (human)	2	1	cerebral degeneration congenital disorder of glycosylation Ip congenital disorder of glycosylation type I congenital disorder of glycosylation epilepsy hypertropia inherited metabolic disorder intellectual disability learning disability mechanical strabismus microcephaly ophthalmoplegia scoliosis sensorineural hearing loss strabismus visual epilepsy
A8MR93	Dol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferase	ALG12 EBS4	Arabidopsis thaliana (thale cress)	2	0
Q9NP73	UDP-N-acetylglucosamine transferase subunit ALG13	ALG13 CXorf45 GLT28D1	Homo sapiens (human)	0	1	Bell's palsy Meckel's diverticulum West syndrome agnosia attention deficit hyperactivity disorder autistic disorder blindness cerebral degeneration choreatic disease clubfoot congenital disorder of glycosylation type I congenital disorder of glycosylation congenital nystagmus craniosynostosis developmental and epileptic encephalopathy 36 dissociated nystagmus epilepsy facial nerve disease facial paralysis focal segmental glomerulosclerosis hypophosphatemia intellectual disability learning disability lung cancer lung non-small cell carcinoma microcephaly non-syndromic X-linked intellectual disability obesity obsolete infantile epileptic encephalopathy optic atrophy pathologic nystagmus placental insufficiency pyloric stenosis spontaneous ocular nystagmus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability type 10 visual epilepsy
Q96F25	UDP-N-acetylglucosamine transferase subunit ALG14	ALG14	Homo sapiens (human)	0	1	Bell's palsy agnosia clubfoot congenital myasthenic syndrome 15 congenital myasthenic syndrome congenital ptosis developmental coordination disorder facial nerve disease facial paralysis familial periodic paralysis idiopathic scoliosis intellectual disability isolated elevated serum creatine phosphokinase levels learning disability myopathy ptosis scoliosis syndromic X-linked intellectual disability 94
Q6BVA4	Alpha-1,3/1,6-mannosyltransferase ALG2	ALG2	Debaryomyces hansenii CBS767	2	0
Q59LF2	Alpha-1,3/1,6-mannosyltransferase ALG2	ALG2	Candida albicans SC5314	3	0
Q755C1	Alpha-1,3/1,6-mannosyltransferase ALG2	ALG2	Eremothecium gossypii ATCC 10895	1	0
Q6FJJ9	Alpha-1,3/1,6-mannosyltransferase ALG2	ALG2	Nakaseomyces glabratus CBS 138	2	0
O94738	Alpha-1,3/1,6-mannosyltransferase ALG2	ALG2	Rhizomucor pusillus	1	0
P43636	Alpha-1,3/1,6-mannosyltransferase ALG2	ALG2	Saccharomyces cerevisiae S288C	4	0
Q6CWQ0	Alpha-1,3/1,6-mannosyltransferase ALG2	ALG2	Kluyveromyces lactis NRRL Y-1140	5	0
Q6C3V7	Alpha-1,3/1,6-mannosyltransferase ALG2	ALG2	Yarrowia lipolytica CLIB122	2	0
O82244	Dol-P-Man:Man(5)GlcNAc(2)-PP-Dol alpha-1,3-mannosyltransferase	ALG3	Arabidopsis thaliana (thale cress)	2	0
Q9Y673	Dolichyl-phosphate beta-glucosyltransferase	ALG5	Homo sapiens (human)	1	1
Q9Y672	Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase	ALG6	Homo sapiens (human)	1	0	antithrombin III deficiency congenital disorder of glycosylation Ia congenital disorder of glycosylation Ic congenital disorder of glycosylation type I congenital disorder of glycosylation epilepsy hypertropia mechanical strabismus ophthalmoplegia protein C deficiency protein S deficiency strabismus thrombophilia visual epilepsy
Q802T2	Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase	ALG6	Gallus gallus (chicken)	1	0
Q5NVS8	Dolichyl pyrophosphate Man9GlcNAc2 alpha-1,3-glucosyltransferase	ALG6	Pongo abelii (Sumatran orangutan)	1	0
Q9H6U8	Alpha-1,2-mannosyltransferase ALG9	ALG9 DIBD1	Homo sapiens (human)	4	2	Gilles de la Tourette syndrome Marfan syndrome Meckel syndrome 1 Meckel syndrome 2 Meckel syndrome 3 Meckel syndrome 4 Meckel syndrome 5 Meckel syndrome 6 Meckel syndrome 8 Meckel syndrome autosomal dominant polycystic kidney disease cardiovascular system disease congenital disorder of glycosylation Il congenital disorder of glycosylation type I congenital disorder of glycosylation congenital heart disease congestive heart failure craniosynostosis cystic kidney disease cystinuria enophthalmos epilepsy esotropia galactokinase deficiency galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease Ia glycogen storage disease heart disease heart septal defect hemopericardium intellectual disability learning disability microcephaly monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia neuroendocrine carcinoma neuroendocrine tumor obsolete exophthalmos orbital disease osteochondrodysplasia pericardial effusion polycystic kidney disease 1 polycystic liver disease psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder situs inversus tuberous sclerosis visual epilepsy
Q9FZ49	Alpha-1,2-mannosyltransferase ALG9	ALG9	Arabidopsis thaliana (thale cress)	1	0
Q9LTW0	ALA-interacting subunit 1	ALIS1	Arabidopsis thaliana (thale cress)	3	0
Q67YS6	Putative ALA-interacting subunit 2	ALIS2	Arabidopsis thaliana (thale cress)	4	0
Q9SLK2	ALA-interacting subunit 3	ALIS3	Arabidopsis thaliana (thale cress)	3	0
Q9SA35	Putative ALA-interacting subunit 4	ALIS4	Arabidopsis thaliana (thale cress)	3	0
Q8L8W0	ALA-interacting subunit 5	ALIS5	Arabidopsis thaliana (thale cress)	2	0
Q9UM73	ALK tyrosine kinase receptor	ALK	Homo sapiens (human)	16	1

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