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 **122901 - 122925** of **126547** in total

« First

‹ Prev

…

4913

4914

4915

4916

4917

4918

4919

4920

4921

…

Next ›

Last »
UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▲	Disease Ontology
Q9NZM1	Myoferlin	MYOF FER1L3 KIAA1207	Homo sapiens (human)	5	2
O94967	WD repeat-containing protein 47	WDR47 KIAA0893	Homo sapiens (human)	1	2
P97445	Voltage-dependent P/Q-type calcium channel subunit alpha-1A	Cacna1a Caca1a Cach4 Cacn3 Cacnl1a4 Ccha1a	Mus musculus (house mouse)	5	2
Q9NUA8	Zinc finger and BTB domain-containing protein 40	ZBTB40 KIAA0478	Homo sapiens (human)	3	2
E9Q743	Cilia- and flagella-associated protein 251	Cfap251 Wdr66	Mus musculus (house mouse)	4	2
Q15113	Procollagen C-endopeptidase enhancer 1	PCOLCE PCPE1	Homo sapiens (human)	4	2
Q9UPP1	Histone lysine demethylase PHF8	PHF8 KIAA1111 ZNF422	Homo sapiens (human)	5	2
Q6ZS30	Neurobeachin-like protein 1	NBEAL1 ALS2CR16 ALS2CR17	Homo sapiens (human)	3	2
Q91XA2	Golgi membrane protein 1	Golm1 Golph2	Mus musculus (house mouse)	3	2
Q0HA38	Tetratricopeptide repeat protein 21B	Ttc21b Ift139 Kiaa1992 Thm1	Mus musculus (house mouse)	1	2
O00268	Transcription initiation factor TFIID subunit 4	TAF4 TAF2C TAF2C1 TAF4A TAFII130 TAFII135	Homo sapiens (human)	22	2
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
Q9DCZ4	MICOS complex subunit Mic26	Apoo Fam121b Mic23 Mic26	Mus musculus (house mouse)	1	2
Q9BRK5	45 kDa calcium-binding protein	SDF4 CAB45	Homo sapiens (human)	9	2
Q96B26	Exosome complex component RRP43	EXOSC8 OIP2 RRP43	Homo sapiens (human)	1	2
P10493	Nidogen-1	Nid1 Ent	Mus musculus (house mouse)	9	2
P10912	Growth hormone receptor	GHR	Homo sapiens (human)	7	2
O15063	Granule associated Rac and RHOG effector protein 1	GARRE1 KIAA0355	Homo sapiens (human)	1	2
Q9WU79	Proline dehydrogenase 1, mitochondrial	Prodh Pro1	Mus musculus (house mouse)	1	2
Q8BGQ7	Alanine--tRNA ligase, cytoplasmic	Aars1 Aars	Mus musculus (house mouse)	1	2
Q8IVL6	Prolyl 3-hydroxylase 3	P3H3 LEPREL2	Homo sapiens (human)	2	2
Q6UWE0	E3 ubiquitin-protein ligase LRSAM1	LRSAM1 TAL	Homo sapiens (human)	1	2
P25440	Bromodomain-containing protein 2	BRD2 KIAA9001 RING3	Homo sapiens (human)	7	2
Q3U3E2	Protein FAM117B	Fam117b Als2cr13	Mus musculus (house mouse)	5	2
E9Q4F7	Ankyrin repeat domain-containing protein 11	Ankrd11	Mus musculus (house mouse)	2	2

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements