GlyCosmos Portal

Source	Last Updated
GlyConnect	April 19, 2023
GlycoProtDB	October 1, 2021
GlyGen	June 4, 2024
The O-GlcNAc Database	June 3, 2024
UniProt	June 4, 2024

Displaying entries **16001 - 16025** of **18496** in total

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UniProt ID	Protein Name ▲	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs	Disease Ontology
O95136	Sphingosine 1-phosphate receptor 2	S1PR2 EDG5	Homo sapiens (human)	1	1
Q99500	Sphingosine 1-phosphate receptor 3	S1PR3 C9orf108 C9orf47 EDG3	Homo sapiens (human)	1	1
O95977	Sphingosine 1-phosphate receptor 4	S1PR4 EDG6	Homo sapiens (human)	2	0
Q9H228	Sphingosine 1-phosphate receptor 5	S1PR5 EDG8	Homo sapiens (human)	1	0
O95470	Sphingosine-1-phosphate lyase 1	SGPL1 KIAA1252	Homo sapiens (human)	1	2	Addison's disease Alzheimer's disease Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Huntington's disease-like 1 Huntington's disease-like 2 Huntington's disease IMAGe syndrome Marfan syndrome Niemann-Pick disease Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome adrenal cortical hypofunction alveolar rhabdomyosarcoma anaplastic astrocytoma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal recessive Robinow syndrome autosomal recessive congenital ichthyosis 1 breast cancer breast carcinoma cancer childhood cerebral astrocytoma chondrodysplasia-pseudohermaphroditism syndrome chronic obstructive pulmonary disease colitis colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital hypothyroidism congenital ptosis congestive heart failure coronary artery disease cryptorchidism embryoma endometrial cancer endometrial carcinoma epilepsy familial nephrotic syndrome fibrillary astrocytoma focal segmental glomerulosclerosis gastroenteritis gemistocytic astrocytoma glucose intolerance high grade glioma hyperglycemia hypertropia hypoglycemia hypogonadism hypothyroidism ichthyosis idiopathic interstitial pneumonia ileitis ileocolitis inherited metabolic disorder juvenile pilocytic astrocytoma keratosis follicularis kidney disease large intestine cancer laryngeal disease lipoid nephrosis lymphopenia malignant astrocytoma mechanical strabismus microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II microcephaly mongolian spot multiple sclerosis myxedema nephrosis nephrotic syndrome type 14 nephrotic syndrome type 1 nephrotic syndrome neurodegenerative disease neuropathy obsolete congenital ichthyosiform erythroderma ophthalmoplegia peripheral nervous system disease pilocytic astrocytoma pneumonia polyneuropathy postinflammatory pulmonary fibrosis prediabetes syndrome proteinuria protoplasmic astrocytoma pseudoxanthoma elasticum ptosis pulmonary fibrosis sensorineural hearing loss situs inversus sphingolipidosis strabismus subependymal giant cell astrocytoma tracheal disease triple-A syndrome tuberous sclerosis uterine corpus cancer visual epilepsy
Q9BX95	Sphingosine-1-phosphate phosphatase 1	SGPP1 SPP1	Homo sapiens (human)	0	1	adult lymphoma cancer colitis embryoma gastroenteritis ileitis ileocolitis inflammatory bowel disease squamous cell carcinoma stomach cancer stomach carcinoma tongue squamous cell carcinoma
A6NFX1	Sphingosine-1-phosphate transporter MFSD2B	MFSD2B	Homo sapiens (human)	0	1
Q8IVW8	Sphingosine-1-phosphate transporter SPNS2	SPNS2	Homo sapiens (human)	0	1
Q8N0Z3	Spindle and centriole-associated protein 1	SPICE1 CCDC52 SPICE	Homo sapiens (human)	3	3
Q8IX90	Spindle and kinetochore-associated protein 3	SKA3 C13orf3 RAMA1	Homo sapiens (human)	1	1
Q6UVJ0	Spindle assembly abnormal protein 6 homolog	SASS6 SAS6	Homo sapiens (human)	6	1
Q9BUA3	Spindlin interactor and repressor of chromatin-binding protein	SPINDOC C11orf84	Homo sapiens (human)	0	1
Q9Y657	Spindlin-1	SPIN1 OCR SPIN	Homo sapiens (human)	0	1
Q99865	Spindlin-2A	SPIN2A DXF34 SPIN2	Homo sapiens (human)	1	1
Q9BPZ2	Spindlin-2B	SPIN2B SPIN2	Homo sapiens (human)	1	1
Q5JUX0	Spindlin-3	SPIN3	Homo sapiens (human)	0	1
Q56A73	Spindlin-4	SPIN4	Homo sapiens (human)	0	1
Q13838	Spliceosome RNA helicase DDX39B	DDX39B BAT1 UAP56	Homo sapiens (human)	0	1
Q9P013	Spliceosome-associated protein CWC15 homolog	CWC15 C11orf5	Homo sapiens (human)	3	2
Q6UX04	Spliceosome-associated protein CWC27 homolog	CWC27 SDCCAG10	Homo sapiens (human)	2	1
Q15637	Splicing factor 1	SF1 ZFM1 ZNF162	Homo sapiens (human)	10	2
Q15459	Splicing factor 3A subunit 1	SF3A1 SAP114	Homo sapiens (human)	1	1
Q15428	Splicing factor 3A subunit 2	SF3A2 SAP62	Homo sapiens (human)	3	1
Q12874	Splicing factor 3A subunit 3	SF3A3 SAP61	Homo sapiens (human)	1	1
O75533	Splicing factor 3B subunit 1	SF3B1 SAP155	Homo sapiens (human)	4	1

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