GlyCosmos Portal

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GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
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Displaying entries **16101 - 16125** 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
Q8NBZ7	UDP-glucuronic acid decarboxylase 1	UXS1	Homo sapiens (human)	1	1	bipolar disorder hereditary multiple exostoses schizoaffective disorder schizophrenia schizophreniform disorder
Q8NBX0	Saccharopine dehydrogenase-like oxidoreductase	SCCPDH	Homo sapiens (human)	0	1
Q8NBW4	Neutral amino acid transporter 9	SLC38A9 URLC11	Homo sapiens (human)	4	0
Q8NBU5	Outer mitochondrial transmembrane helix translocase	ATAD1	Homo sapiens (human)	1	2
Q8NBT3	Transmembrane protein 145	TMEM145	Homo sapiens (human)	2	2
Q8NBS9	Thioredoxin domain-containing protein 5	TXNDC5 TLP46	Homo sapiens (human)	14	6
Q8NBS3	Solute carrier family 4 member 11	SLC4A11 BTR1	Homo sapiens (human)	2	0
Q8NBR9	Uncharacterized protein NDUFV1-DT	NDUFV1-DT C11orf72	Homo sapiens (human)	0	1
Q8NBR0	Tumor protein p53-inducible protein 13	TP53I13 DSCP1	Homo sapiens (human)	9	3
Q8NBQ5	Estradiol 17-beta-dehydrogenase 11	HSD17B11 DHRS8 PAN1B SDR16C2	Homo sapiens (human)	1	1
Q8NBP7	Proprotein convertase subtilisin/kexin type 9	PCSK9 NARC1	Homo sapiens (human)	1	1
Q8NBP5	Major facilitator superfamily domain-containing protein 9	MFSD9	Homo sapiens (human)	1	1
Q8NBN7	Retinol dehydrogenase 13	RDH13 SDR7C3	Homo sapiens (human)	0	1
Q8NBN3	Transmembrane protein 87A	TMEM87A	Homo sapiens (human)	6	41
Q8NBM8	Prenylcysteine oxidase-like	PCYOX1L	Homo sapiens (human)	1	0
Q8NBM4	Ubiquitin-associated domain-containing protein 2	UBAC2 PHGDHL1	Homo sapiens (human)	1	1
Q8NBL3	Transmembrane protein 178A	TMEM178A TMEM178	Homo sapiens (human)	1	0
Q8NBL1	Protein O-glucosyltransferase 1	POGLUT1 C3orf9 CLP46 KTELC1 MDSRP	Homo sapiens (human)	5	23	Dowling-Degos disease Duchenne muscular dystrophy T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia acute myeloid leukemia 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 cancer childhood T-cell acute lymphoblastic leukemia childhood leukemia colon cancer colon carcinoma colonic benign neoplasm colorectal cancer colorectal carcinoma congenital muscular dystrophy distal myopathy embryoma essential thrombocythemia facioscapulohumeral muscular dystrophy hematopoietic system disease isolated elevated serum creatine phosphokinase levels keratosis follicularis large intestine cancer leukemia limb-girdle muscular dystrophy lung cancer lung non-small cell carcinoma mongolian spot muscular dystrophy myelodysplastic syndrome myofibrillar myopathy 1 myofibrillar myopathy 3 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 primary biliary cholangitis pseudoxanthoma elasticum reticulate acropigmentation of Kitamura rippling muscle disease 2
Q8NBK3	Formylglycine-generating enzyme	SUMF1	Homo sapiens (human)	2	12	Balo concentric sclerosis Laron syndrome X-linked chondrodysplasia punctata 1 X-linked ichthyosis achondroplasia adrenoleukodystrophy autosomal dominant cerebellar ataxia autosomal dominant chondrodysplasia punctata autosomal recessive spinocerebellar ataxia 16 blindness breast cancer breast carcinoma cancer cataract central nervous system disease cerebral degeneration chondrodysplasia punctata chronic obstructive pulmonary disease communicating hydrocephalus cystic fibrosis embryoma epilepsy hydrocephalus ichthyosis inherited metabolic disorder intellectual disability learning disability lysosomal storage disease metachromatic leukodystrophy microcephaly mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis mucosulfatidosis multiple sclerosis narcolepsy obstructive hydrocephalus optic atrophy recurrent corneal erosion retinal degeneration rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 schizophrenia senile degeneration of brain sensorineural hearing loss visual epilepsy
Q8NBJ9	SID1 transmembrane family member 2	SIDT2	Homo sapiens (human)	11	8
Q8NBJ7	Inactive C-alpha-formylglycine-generating enzyme 2	SUMF2	Homo sapiens (human)	6	21
Q8NBJ5	Procollagen galactosyltransferase 1	COLGALT1 GLT25D1	Homo sapiens (human)	5	31	Balo concentric sclerosis Simpson-Golabi-Behmel syndrome type 1 adrenoleukodystrophy bone osteosarcoma central nervous system disease cerebral degeneration childhood osteosarcoma epilepsy locked-in syndrome narcolepsy osteosarcoma porencephaly quadriplegia visual epilepsy
Q8NBJ4	Golgi membrane protein 1	GOLM1 C9orf155 GOLPH2	Homo sapiens (human)	18	61
Q8NBI6	Xyloside xylosyltransferase 1	XXYLT1 C3orf21	Homo sapiens (human)	4	2	atrial fibrillation bronchus cancer bronchus carcinoma cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma nicotine dependence obesity osteoporosis
Q8NBI5	Equilibrative nucleobase transporter 1	SLC43A3 ENBT1	Homo sapiens (human)	4	4

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