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 **18326 - 18350** 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
O43426	Synaptojanin-1	SYNJ1 KIAA0910	Homo sapiens (human)	7	1	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Creutzfeldt-Jakob disease Down syndrome Duchenne muscular dystrophy Joubert syndrome 1 Joubert syndrome Laron syndrome Parkinson's disease 19A Parkinson's disease 1 Parkinson's disease 20 Parkinson's disease 23 Parkinson's disease 2 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome Unverricht-Lundborg syndrome achondroplasia amnestic disorder amyotrophic lateral sclerosis anodontia attention deficit hyperactivity disorder autistic disorder 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 bipolar disorder blepharospasm blindness borderline personality disorder brain disease cerebral degeneration cone-rod dystrophy congenital muscular dystrophy congenital nystagmus congenital ptosis dementia developmental and epileptic encephalopathy 1 developmental and epileptic encephalopathy 53 dissociated nystagmus distal myopathy dystonia early infantile epileptic encephalopathy early myoclonic encephalopathy early-onset Parkinson's disease epilepsy esophagitis facioscapulohumeral muscular dystrophy focal hand dystonia fundus albipunctatus gastroesophageal reflux disease giant cell glioblastoma glioblastoma high grade glioma intellectual disability intermittent explosive disorder isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia locked-in syndrome microcephaly muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 neuroblastoma neurodegenerative disease 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 obsolete infantile epileptic encephalopathy oculopharyngeal muscular dystrophy optic atrophy pathologic nystagmus peptic esophagitis progressive muscular atrophy ptosis quadriplegia retinal degeneration retinitis pigmentosa retrograde amnesia rhabdomyosarcoma rippling muscle disease 2 scoliosis secondary Parkinson disease spontaneous ocular nystagmus status epilepticus tauopathy tooth agenesis visual epilepsy
I3ZN85	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
A8MWD9	Putative small nuclear ribonucleoprotein G-like protein 15	SNRPGP15	Homo sapiens (human)	1	1
Q9P0X4	Voltage-dependent T-type calcium channel subunit alpha-1I	CACNA1I KIAA1120	Homo sapiens (human)	7	1
Q9BYM8	RanBP-type and C3HC4-type zinc finger-containing protein 1	RBCK1 C20orf18 RNF54 UBCE7IP3 XAP3 XAP4	Homo sapiens (human)	0	1
Q9BVV7	Mitochondrial import inner membrane translocase subunit Tim21	TIMM21 C18orf55 TIM21	Homo sapiens (human)	2	1
F8SY67	MHC class I antigen (Fragment)	HLA-Cw	Homo sapiens (human)	1	0
Q9H3R5	Centromere protein H	CENPH ICEN35	Homo sapiens (human)	0	1
D7GK37	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
Q9NX65	Zinc finger and SCAN domain-containing protein 32	ZSCAN32 ZNF434	Homo sapiens (human)	0	1
P43116	Prostaglandin E2 receptor EP2 subtype	PTGER2	Homo sapiens (human)	4	0
F8RHF2	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
P78545	ETS-related transcription factor Elf-3	ELF3 ERT ESX JEN	Homo sapiens (human)	0	1
Q14050	Collagen alpha-3(IX) chain	COL9A3	Homo sapiens (human)	1	0
F2VP88	MHC class I antigen (Fragment)	HLA-C	Homo sapiens (human)	1	0
A0A1S5QQY5	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
I3UI71	MHC class I antigen (Fragment)	HLA-B	Homo sapiens (human)	1	0
Q9HCY8	Protein S100-A14	S100A14 S100A15	Homo sapiens (human)	0	1
B7ZL68	Neuropilin	NRP2	Homo sapiens (human)	2	0
Q15046	Lysine--tRNA ligase	KARS1 KARS KIAA0070	Homo sapiens (human)	2	1
A0A4P2SSX2	MHC class I antigen	HLA-B	Homo sapiens (human)	1	0
Q9ULD8	Potassium voltage-gated channel subfamily H member 3	KCNH3 KIAA1282	Homo sapiens (human)	4	1
P20138	Myeloid cell surface antigen CD33	CD33 SIGLEC3	Homo sapiens (human)	9	4	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease B-cell lymphoma Burkitt lymphoma Creutzfeldt-Jakob disease Crohn's colitis Crohn's disease Fanconi anemia complementation group A Fanconi anemia Japanese encephalitis Langerhans-cell histiocytosis Miller-Dieker lissencephaly syndrome Pick's disease Reye syndrome Richter's syndrome St. Louis encephalitis Stevens-Johnson syndrome T-cell acute lymphoblastic leukemia T-cell adult acute lymphocytic leukemia T-cell childhood lymphoblastic lymphoma acoustic neuroma acute biphenotypic leukemia acute leukemia acute lymphoblastic leukemia acute monocytic leukemia acute myeloid leukemia acute promyelocytic leukemia adult acute lymphocytic leukemia adult lymphoma aggressive systemic mastocytosis agranulocytosis allergic asthma amyloidosis angiomatous meningioma asthma atypical chronic myeloid leukemia, BCR-ABL1 negative benign meningioma bone marrow cancer breast cancer breast carcinoma bronchus cancer bronchus carcinoma cancer carcinoma central nervous system lymphoma cerebral convexity meningioma cerebral degeneration childhood T-cell acute lymphoblastic leukemia childhood acute lymphocytic leukemia childhood acute myeloid leukemia childhood leukemia childhood lymphoma chromosome 17p13.1 deletion syndrome chronic lymphocytic leukemia chronic monocytic leukemia chronic myeloid leukemia chronic obstructive pulmonary disease clear cell meningioma colorectal cancer colorectal carcinoma dengue disease diabetes mellitus diabetic ketoacidosis embryoma essential thrombocythemia fibrous meningioma giant cell glioblastoma glioblastoma head and neck squamous cell carcinoma hepatitis C high grade glioma hyperglycemia in situ carcinoma indolent systemic mastocytosis inflammatory bowel disease 1 inflammatory bowel disease intraorbital meningioma intraventricular meningioma intrinsic asthma large intestine cancer leukemia leukopenia lissencephaly lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoblastic lymphoma lymphoid leukemia lymphoma mast-cell leukemia mastocytosis meningioma meningothelial meningioma microcystic meningioma multiple myeloma myelodysplastic syndrome myeloid leukemia myeloid sarcoma myeloproliferative neoplasm neurodegenerative disease neuroendocrine carcinoma neuroendocrine tumor neutropenia non-Hodgkin lymphoma obesity obsolete ymphosarcoma olfactory groove meningioma ovarian cancer ovarian carcinoma parasagittal meningioma pituitary adenoma plasmacytoma polycythemia vera polycythemia primary immunodeficiency disease prostate cancer prostate carcinoma psammomatous meningioma reticulosarcoma secretory meningioma severe congenital neutropenia spinal meningioma squamous cell carcinoma status epilepticus stomach cancer stomach carcinoma systemic lupus erythematosus systemic mastocytosis tongue squamous cell carcinoma transitional meningioma type 2 diabetes mellitus ulcerative colitis viral infectious disease yellow fever
C9JN98	Serpin family E member 2 (Fragment)	SERPINE2	Homo sapiens (human)	1	0
P17098	Zinc finger protein 8	ZNF8	Homo sapiens (human)	0	1

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