GlyCosmos Portal

GlyCosmos Glycoproteins

Integrated list of glycoproteins extracted from UniProt and annotated with glycosylation data from GlyGen, GlyConnect, GlycoProtDB and The O-GlcNAc Database. For each entry, information such as glycosylation site, glycans, diseases, 3D structures, and pathway information are available.

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 **14151 - 14175** 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
Q92562	Polyphosphoinositide phosphatase	FIG4 KIAA0274 SAC3	Homo sapiens (human)	1	1	Charcot-Marie-Tooth disease X-linked dominant 1 Charcot-Marie-Tooth disease X-linked dominant 6 Charcot-Marie-Tooth disease X-linked recessive 2 Charcot-Marie-Tooth disease X-linked recessive 3 Charcot-Marie-Tooth disease X-linked recessive 4 Charcot-Marie-Tooth disease X-linked recessive 5 Charcot-Marie-Tooth disease axonal type 2C Charcot-Marie-Tooth disease axonal type 2F Charcot-Marie-Tooth disease axonal type 2H Charcot-Marie-Tooth disease axonal type 2K Charcot-Marie-Tooth disease axonal type 2L Charcot-Marie-Tooth disease axonal type 2N Charcot-Marie-Tooth disease axonal type 2O Charcot-Marie-Tooth disease axonal type 2P Charcot-Marie-Tooth disease axonal type 2Q Charcot-Marie-Tooth disease axonal type 2T Charcot-Marie-Tooth disease axonal type 2U Charcot-Marie-Tooth disease dominant intermediate A Charcot-Marie-Tooth disease dominant intermediate B Charcot-Marie-Tooth disease dominant intermediate C Charcot-Marie-Tooth disease dominant intermediate D Charcot-Marie-Tooth disease dominant intermediate E Charcot-Marie-Tooth disease dominant intermediate F Charcot-Marie-Tooth disease recessive intermediate B Charcot-Marie-Tooth disease recessive intermediate C Charcot-Marie-Tooth disease recessive intermediate D Charcot-Marie-Tooth disease type 1A Charcot-Marie-Tooth disease type 1B Charcot-Marie-Tooth disease type 1C Charcot-Marie-Tooth disease type 1D Charcot-Marie-Tooth disease type 1E Charcot-Marie-Tooth disease type 1F Charcot-Marie-Tooth disease type 2 Charcot-Marie-Tooth disease type 2A1 Charcot-Marie-Tooth disease type 2A2A Charcot-Marie-Tooth disease type 2B1 Charcot-Marie-Tooth disease type 2B2 Charcot-Marie-Tooth disease type 2B Charcot-Marie-Tooth disease type 2D Charcot-Marie-Tooth disease type 2E Charcot-Marie-Tooth disease type 2I Charcot-Marie-Tooth disease type 2J Charcot-Marie-Tooth disease type 2R Charcot-Marie-Tooth disease type 2Y Charcot-Marie-Tooth disease type 3 Charcot-Marie-Tooth disease type 4 Charcot-Marie-Tooth disease type 4A Charcot-Marie-Tooth disease type 4B1 Charcot-Marie-Tooth disease type 4B2 Charcot-Marie-Tooth disease type 4B3 Charcot-Marie-Tooth disease type 4C Charcot-Marie-Tooth disease type 4D Charcot-Marie-Tooth disease type 4E Charcot-Marie-Tooth disease type 4F Charcot-Marie-Tooth disease type 4G Charcot-Marie-Tooth disease type 4H Charcot-Marie-Tooth disease type 4J Charcot-Marie-Tooth disease type 4K Charcot-Marie-Tooth disease Joubert syndrome Laron syndrome Marfan syndrome Miller-Dieker lissencephaly syndrome Papillon-Lefevre disease Yunis-Varon syndrome achondroplasia agenesis of the corpus callosum with peripheral neuropathy amyotrophic lateral sclerosis type 11 amyotrophic lateral sclerosis type 1 amyotrophic lateral sclerosis type 2 amyotrophic lateral sclerosis type 4 amyotrophic lateral sclerosis anterior horn cell disease anxiety disorder atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal recessive distal hereditary motor neuronopathy 1 breast cancer breast carcinoma cardiomyopathy cataract communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 cortical dysplasia-focal epilepsy syndrome cryptorchidism demyelinating disease demyelinating polyneuropathy depressive disorder distal arthrogryposis dysthymic disorder endomyocardial fibrosis enophthalmos epilepsy essential hypertension generalized anxiety disorder gingival recession gliosarcoma hereditary neuropathy with liability to pressure palsies hereditary sensory and autonomic neuropathy type 1 hereditary sensory and autonomic neuropathy type 2 hereditary spastic paraplegia 7 high grade glioma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hypertension hypertrophic cardiomyopathy hypospadias laryngostenosis lateral sclerosis lissencephaly lysosomal storage disease major depressive disorder melancholic depression microcephaly mixed glioma motor neuron disease motor peripheral neuropathy neuroblastoma neurodegenerative disease neuropathy neurotic disorder obsolete exophthalmos obsolete hereditary motor and sensory neuropathy with agenesis of the corpus callosum obsolete melancholia obstructive hydrocephalus orbital disease patent foramen ovale peripheral nervous system disease placental insufficiency polyhydramnios polyneuropathy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 primary pulmonary hypertension progressive muscular atrophy pyloric stenosis renal artery obstruction renovascular hypertension sclerocornea senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus status epilepticus subacute delirium syndactyly syndromic X-linked intellectual disability Najm type tetralogy of Fallot tuberous sclerosis ventricular septal defect
Q9BVA6	Protein adenylyltransferase FICD	FICD HIP13 HYPE	Homo sapiens (human)	2	2
Q8TAL6	Fin bud initiation factor homolog	FIBIN	Homo sapiens (human)	1	0
Q8N539	Fibrinogen C domain-containing protein 1	FIBCD1	Homo sapiens (human)	1	0
Q2V2M9	FH1/FH2 domain-containing protein 3	FHOD3 FHOS2 KIAA1695	Homo sapiens (human)	1	1
Q9Y613	FH1/FH2 domain-containing protein 1	FHOD1 FHOS FHOS1	Homo sapiens (human)	1	1
Q13643	Four and a half LIM domains protein 3	FHL3 SLIM2	Homo sapiens (human)	1	1
Q14192	Four and a half LIM domains protein 2	FHL2 DRAL SLIM3	Homo sapiens (human)	0	1
Q13642	Four and a half LIM domains protein 1	FHL1 SLIM1	Homo sapiens (human)	2	2
Q5W0V3	FHF complex subunit HOOK interacting protein 2A	FHIP2A FAM160B1 KIAA1600	Homo sapiens (human)	0	1
B1AJZ9	Forkhead-associated domain-containing protein 1	FHAD1 KIAA1937	Homo sapiens (human)	4	1
P07954	Fumarate hydratase, mitochondrial	FH	Homo sapiens (human)	1	1	B-cell lymphoma Barrett's esophagus Burkitt lymphoma Crohn's colitis Crohn's disease Gilbert syndrome Hirschsprung's disease Langerhans-cell histiocytosis MELAS syndrome Parkinson's disease Richter's syndrome Tangier disease acquired polycythemia actinic keratosis acute lymphoblastic leukemia acute myeloid leukemia acute promyelocytic leukemia adenosarcoma adrenal carcinoma adrenal cortex cancer adrenal gland cancer adrenal gland hyperfunction adrenocortical carcinoma adult acute lymphocytic leukemia adult lymphoma aggressive systemic mastocytosis agranulocytosis aniridia aortic valve disease 2 aortic valve stenosis arthritis arthropathy autism spectrum disorder autistic disorder autoimmune disease autoimmune hepatitis autoimmune lymphoproliferative syndrome type 2A autoimmune lymphoproliferative syndrome type 2B autoimmune lymphoproliferative syndrome type 3 autoimmune lymphoproliferative syndrome bilirubin metabolic disorder bizarre leiomyoma bladder carcinoma blindness brain disease breast cancer cancer carcinoma cataract central nervous system lymphoma cerebral degeneration cerebral malaria childhood acute lymphocytic leukemia childhood kidney cell carcinoma childhood lymphoma cholestasis chromophobe renal cell carcinoma chronic lymphocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital adrenal hyperplasia congestive heart failure cutaneous leiomyosarcoma cutaneous leishmaniasis cystic kidney disease duodenum cancer embryoma endometrial cancer endometrial carcinoma epilepsy epithelioid leiomyosarcoma erythropoietin polycythemia familial adenomatous polyposis familial erythrocytosis 2 familial renal papillary carcinoma follicular lymphoma fumarase deficiency glomerulonephritis heart cancer hemangioblastoma hypercalcemia hypertensive retinopathy immune system disease indolent systemic mastocytosis inflammatory bowel disease 1 inflammatory bowel disease kidney cancer kidney disease kwashiorkor lactic acidosis large intestine cancer late onset Parkinson's disease leiomyoma cutis leiomyoma leiomyomatosis leiomyosarcoma leukopenia lymphoma lymphoproliferative syndrome 1 lymphoproliferative syndrome 2 mantle cell lymphoma marasmus mastocytosis microcephaly microphthalmia mucinous ovarian cystadenoma mucocutaneous leishmaniasis multiple endocrine neoplasia type 2A multiple myeloma multiple sclerosis muscle benign neoplasm muscle cancer myofibroma myxoid leiomyosarcoma nasopharynx carcinoma nephritis nephroblastoma nephrocalcinosis neuroblastoma neuroendocrine carcinoma neurofibromatosis 1 neurofibromatosis neutropenia non-Hodgkin lymphoma non-congenital cyst of kidney nonpapillary renal cell carcinoma nutrition disease obsolete Cushing's syndrome obsolete ymphosarcoma optic atrophy osteoarthritis oxyphilic adenoma pancreatic cancer pancreatic carcinoma panic disorder papillary adenocarcinoma papillary renal cell carcinoma paraganglioma pheochromocytoma phosphorus metabolism disease polycythemia vera polycythemia primary biliary cholangitis primary hyperaldosteronism prostate cancer prostate carcinoma protein-energy malnutrition proteinuria rectal benign neoplasm rectum adenocarcinoma rectum cancer renal carcinoma renal cell carcinoma renal osteodystrophy reticulosarcoma sarcomatoid carcinoma sarcomatoid renal cell carcinoma schizophrenia seborrheic keratosis severe congenital neutropenia sickle cell anemia skin disease small intestine cancer smooth muscle tumor speech disorder status epilepticus stomach cancer stomach carcinoma stress polycythemia systemic Epstein-Barr virus positive T-cell lymphoma of childhood systemic lupus erythematosus systemic mastocytosis testicular cancer thyroid adenoma thyroid cancer thyroid gland carcinoma thyroid gland papillary carcinoma trichohepatoenteric syndrome 1 trichohepatoenteric syndrome ulcerative colitis urinary bladder cancer uterine corpus cancer uterine fibroid uterus leiomyosarcoma vaginal cancer visceral leishmaniasis visual epilepsy
P09769	Tyrosine-protein kinase Fgr	FGR SRC2	Homo sapiens (human)	2	1
Q14314	Fibroleukin	FGL2	Homo sapiens (human)	7	126
P02679	Fibrinogen gamma chain	FGG	Homo sapiens (human)	3	107
C9JC84	Fibrinogen gamma chain	FGG	Homo sapiens (human)	1	0
C9JEU5	Fibrinogen gamma chain	FGG	Homo sapiens (human)	1	0
A0PJ49	FGFRL1 protein (Fragment)	FGFRL1	Homo sapiens (human)	1	0
Q8N441	Fibroblast growth factor receptor-like 1	FGFRL1 FGFR5 FHFR	Homo sapiens (human)	4	5
B5A965	Soluble FGFR4 variant 2	FGFR4	Homo sapiens (human)	1	0
J3KPQ0	Fibroblast growth factor receptor	FGFR4	Homo sapiens (human)	1	0
P22455	Fibroblast growth factor receptor 4	FGFR4 JTK2 TKF	Homo sapiens (human)	8	10
A0A7I2RW32	Fibroblast growth factor receptor	FGFR3	Homo sapiens (human)	2	0
Q8NI16	Fibroblast growth factor receptor 3 (Fragment)	FGFR3	Homo sapiens (human)	2	0
X5D2G8	Fibroblast growth factor receptor 3 (Fragment)	FGFR3	Homo sapiens (human)	2	0

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