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 **2626 - 2650** 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
G9I2L1	MHC Class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
A0A6B7IHH5	MHC class I antigen	HLA-C	Homo sapiens (human)	1	0
O60927	E3 ubiquitin-protein ligase PPP1R11	PPP1R11 HCGV TCTE5	Homo sapiens (human)	2	1
P31327	Carbamoyl-phosphate synthase [ammonia], mitochondrial	CPS1	Homo sapiens (human)	7	5
A6NDH6	Olfactory receptor 5H15	OR5H15	Homo sapiens (human)	1	0
Q8N335	Glycerol-3-phosphate dehydrogenase 1-like protein	GPD1L KIAA0089	Homo sapiens (human)	0	1	Brugada syndrome 1 Brugada syndrome 2 Brugada syndrome 3 Brugada syndrome 4 Brugada syndrome 5 Brugada syndrome 6 Brugada syndrome 7 Brugada syndrome 8 Brugada syndrome 9 Brugada syndrome arteriosclerotic cardiovascular disease arthritis arthropathy atherosclerosis atrial fibrillation congestive heart failure coronary artery disease head and neck squamous cell carcinoma nutmeg liver osteoarthritis sick sinus syndrome steatotic liver disease sudden infant death syndrome
P30085	UMP-CMP kinase	CMPK1 CMK CMPK UCK UMK UMPK	Homo sapiens (human)	4	1
Q14207	Protein NPAT	NPAT CAND3 E14	Homo sapiens (human)	4	1
P43897	Elongation factor Ts, mitochondrial	TSFM	Homo sapiens (human)	0	1
Q9BZE4	GTP-binding protein 4	GTPBP4 CRFG NOG1	Homo sapiens (human)	1	1
H0YGP2	Adhesion G protein-coupled receptor G6 (Fragment)	ADGRG6	Homo sapiens (human)	1	0
P0C623	Olfactory receptor 4Q2	OR4Q2 OR4Q2P	Homo sapiens (human)	1	0
Q9Y210	Short transient receptor potential channel 6	TRPC6 TRP6	Homo sapiens (human)	5	5
Q15054	DNA polymerase delta subunit 3	POLD3 KIAA0039	Homo sapiens (human)	3	1
P32238	Cholecystokinin receptor type A	CCKAR CCKRA	Homo sapiens (human)	3	0
A0A075B6N1	T cell receptor beta variable 19	TRBV19	Homo sapiens (human)	1	0
P35410	Mas-related G-protein coupled receptor MRG	MAS1L MRG	Homo sapiens (human)	2	0
Q01968	Inositol polyphosphate 5-phosphatase OCRL	OCRL OCRL1	Homo sapiens (human)	1	1	Bartter disease Conn's syndrome Dent disease Ehlers-Danlos syndrome Fanconi anemia Fanconi syndrome Laron syndrome Waterhouse-Friderichsen syndrome achondroplasia amblyopia anemia angular cheilitis anxiety disorder arthritis arthropathy attention deficit hyperactivity disorder autistic disorder autoimmune hemolytic anemia azoospermia blindness buphthalmos calcinosis calcium metabolism disease cataract 1 multiple types cataract 10 multiple types cataract 11 multiple types cataract 12 multiple types cataract 13 with adult i phenotype cataract 14 multiple types cataract 15 multiple types cataract 16 multiple types cataract 17 multiple types cataract 18 cataract 19 multiple types cataract 2 multiple types cataract 20 multiple types cataract 21 multiple types cataract 22 multiple types cataract 23 cataract 24 cataract 25 cataract 26 multiple types cataract 27 cataract 29 cataract 3 multiple types cataract 30 cataract 31 multiple types cataract 32 multiple types cataract 33 cataract 34 multiple types cataract 35 cataract 37 cataract 38 cataract 39 multiple types cataract 4 multiple types cataract 40 cataract 41 cataract 42 cataract 43 cataract 44 cataract 45 cataract 46 juvenile-onset cataract 5 multiple types cataract 6 multiple types cataract 7 cataract 8 multiple types cataract 9 multiple types cataract cheilitis chromosome 17p13.1 deletion syndrome chronic kidney disease chronic ulcer of skin congenital nystagmus cryptorchidism cystinosis dental caries dental enamel hypoplasia dentin caries depressive disorder diabetes insipidus dissociated nystagmus dysthymic disorder epilepsy esophagitis fetal erythroblastosis gastroesophageal reflux disease generalized anxiety disorder giant cell glioblastoma gingivitis glaucoma glioblastoma glomerulonephritis high grade glioma hydrocephalus hydrophthalmos hypercalcemia hyperparathyroidism hypertropia hypokalemia hypophosphatemia inguinal hernia intellectual disability isolated elevated serum creatine phosphokinase levels kidney failure learning disability lip disease lissencephaly listeriosis macrocytic anemia major depressive disorder mechanical strabismus melancholic depression microphthalmia neonatal anemia nephritis nephrocalcinosis nephrolithiasis neurohypophyseal diabetes insipidus neurotic disorder obsolete constipation obsolete melancholia oculocerebrorenal syndrome omphalocele ophthalmoplegia osteitis fibrosa osteoarthritis osteogenesis imperfecta osteomalacia otitis media pathologic nystagmus peptic esophagitis periodontitis phosphorus metabolism disease primary hyperaldosteronism proteinuria recurrent corneal erosion renal tubular acidosis rickets scoliosis skin benign neoplasm skin cancer spondyloepimetaphyseal dysplasia, Sponastrime type spontaneous ocular nystagmus stereotypic movement disorder strabismic amblyopia strabismus subcortical band heterotopia thrombocytopenia trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tropical sprue umbilical hernia uremia uric acid nephrolithiasis visual epilepsy
P07942	Laminin subunit beta-1	LAMB1	Homo sapiens (human)	18	135
M9P9N1	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q96NL6	Sodium channel and clathrin linker 1	SCLT1 SAP1	Homo sapiens (human)	0	1
H0YA68	Alpha-mannosidase (Fragment)	MAN2B2	Homo sapiens (human)	2	0
A0A2H4FZP6	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9UGP8	Translocation protein SEC63 homolog	SEC63 DNAJC23 SEC63L	Homo sapiens (human)	1	1
A0A0X7YJ37	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0

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