GlyCosmos Portal

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Displaying entries **11451 - 11475** of **126547** in total

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UniProt ID	Protein Name	Gene Symbol	Organism	No. of Glycosylation Sites	No. of GlyTouCan IDs ▼	Disease Ontology
V5B780	3-hydroxy-3-methylglutaryl coenzyme A reductase	TCDM_02105	Trypanosoma cruzi Dm28c	0	1
O00499	Myc box-dependent-interacting protein 1	BIN1 AMPHL	Homo sapiens (human)	2	1
P05204	Non-histone chromosomal protein HMG-17	HMGN2 HMG17	Homo sapiens (human)	0	1
K2MLW4	Alpha-MPP	MOQ_009654	Trypanosoma cruzi marinkellei	0	1
F2Z3F1	Uncharacterized protein C5orf67	C5orf67	Homo sapiens (human)	0	1
P31689	DnaJ homolog subfamily A member 1	DNAJA1 DNAJ2 HDJ2 HSJ2 HSPF4	Homo sapiens (human)	0	1
P51826	AF4/FMR2 family member 3	AFF3 LAF4	Homo sapiens (human)	5	1
Q2V2Q1	Antisense of depressing factor protein 1	ADF1	Saccharomyces cerevisiae S288C	3	1
Q96FQ6	Protein S100-A16	S100A16 S100F	Homo sapiens (human)	0	1
Q62812	Myosin-9	Myh9	Rattus norvegicus (Norway rat)	0	1
B6KH13	P-type phospholipid transporter	BN1205_004110	Toxoplasma gondii VEG	0	1
V5B1R9	DRBM domain-containing protein	TCDM_04320	Trypanosoma cruzi Dm28c	0	1
V5C1M1	Pyruvate kinase	TCDM_00417	Trypanosoma cruzi Dm28c	0	1
P20029	Endoplasmic reticulum chaperone BiP	Hspa5 Grp78	Mus musculus (house mouse)	1	1
P43034	Platelet-activating factor acetylhydrolase IB subunit beta	PAFAH1B1 LIS1 MDCR MDS PAFAHA	Homo sapiens (human)	0	1	3p deletion syndrome Alzheimer's disease Angelman syndrome B-cell lymphoma Behcet's disease Crohn's colitis Crohn's disease Ewing sarcoma Gaucher's disease type I Gaucher's disease Hodgkin's granuloma Hodgkin's lymphoma, lymphocytic depletion Hodgkin's lymphoma, lymphocytic-histiocytic predominance Hodgkin's lymphoma, mixed cellularity Hodgkin's lymphoma Joubert syndrome Langerhans-cell histiocytosis Marfan syndrome Miller-Dieker lissencephaly syndrome NFIA-related disorder Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease REM sleep behavior disorder Rett syndrome SATB2-associated syndrome Shwachman-Diamond syndrome Smith-Magenis syndrome West syndrome X-linked juvenile retinoschisis 1 Zellweger syndrome acute monocytic leukemia acute myeloid leukemia adult medulloblastoma adult respiratory distress syndrome aggressive periodontitis allergic asthma alternating hemiplegia of childhood anxiety disorder aplastic anemia asthma autism spectrum disorder autistic disorder autonomic neuropathy bone marrow cancer bone osteosarcoma bronchus cancer bronchus carcinoma cancer central nervous system disease childhood acute myeloid leukemia childhood leukemia childhood medulloblastoma childhood osteosarcoma chromophobe renal cell carcinoma chromosome 13q14 deletion syndrome chromosome 15q13.3 microdeletion syndrome chromosome 15q24 deletion syndrome chromosome 15q26-qter deletion syndrome chromosome 16p11.2 deletion syndrome, 220-kb chromosome 16p12.2-p11.2 deletion syndrome chromosome 17p13.1 deletion syndrome chromosome 17p13.3 duplication syndrome chromosome 17q12 deletion syndrome chromosome 17q23.1-q23.2 deletion syndrome chromosome 18q deletion syndrome chromosome 1q21.1 deletion syndrome chromosome 1q41-q42 deletion syndrome chromosome 2p16.1-p15 deletion syndrome chromosome 6pter-p24 deletion syndrome chromosome 8q21.11 deletion syndrome chromosome 9p deletion syndrome chronic monocytic leukemia chronic myelomonocytic leukemia clear cell renal cell carcinoma collecting duct carcinoma coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congestive heart failure cortical dysplasia-focal epilepsy syndrome dementia depressive disorder distal 10q deletion syndrome distal arthrogryposis dysthymic disorder dystonia embryoma epilepsy essential thrombocythemia essential tremor familial adenomatous polyposis 1 familial adenomatous polyposis generalized anxiety disorder giant cell glioblastoma glioblastoma glomerulonephritis hematologic cancer hepatocellular carcinoma high grade glioma hydranencephaly hydrocephalus impulse control disorder inclusion body myositis inflammatory bowel disease 1 inflammatory bowel disease inguinal hernia intellectual disability intermittent explosive disorder intrinsic asthma islet cell tumor juvenile myelomonocytic leukemia kidney disease kleptomania late onset Parkinson's disease learning disability leukemia lingual-facial-buccal dyskinesia lissencephaly liver cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma lymphoma major depressive disorder medulloblastoma medullomyoblastoma melancholic depression melanotic medulloblastoma microcephaly mood disorder movement disease multiple myeloma multiple system atrophy myelodysplastic syndrome myelodysplastic/myeloproliferative neoplasm myeloproliferative neoplasm nephritis nephrosis nervous system disease neurotic disorder newborn respiratory distress syndrome non-Hodgkin lymphoma nonpapillary renal cell carcinoma obsolete constipation obsolete infantile epileptic encephalopathy obsolete melancholia obsolete ymphosarcoma obstructive hydrocephalus oculocerebrorenal syndrome omphalocele osteosarcoma papillary renal cell carcinoma periodontosis periventricular nodular heterotopia peroxisome biogenesis disorder 1A phobic disorder polycystic ovary syndrome polyhydramnios pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 postural orthostatic tachycardia syndrome progressive supranuclear palsy psychotic disorder pyoureter renal carcinoma renal cell carcinoma reticulosarcoma retinitis pigmentosa 13 sarcomatoid renal cell carcinoma schizoaffective disorder schizophrenia schizophreniform disorder secondary Parkinson disease senile degeneration of brain septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly situs inversus speech disorder subcortical band heterotopia syndromic X-linked intellectual disability Najm type trichohepatoenteric syndrome 1 trichohepatoenteric syndrome tuberous sclerosis ulcerative colitis umbilical hernia vascular disease visual epilepsy
Q13765	Nascent polypeptide-associated complex subunit alpha	NACA	Homo sapiens (human)	0	1
Q96RT6	cTAGE family member 2	CTAGE1 CTAGE2	Homo sapiens (human)	0	1
P61009	Signal peptidase complex subunit 3	SPCS3 SPC22	Homo sapiens (human)	1	1
P80315	T-complex protein 1 subunit delta	Cct4 Cctd	Mus musculus (house mouse)	0	1
Q9BVI0	PHD finger protein 20	PHF20 C20orf104 GLEA2 HCA58 NZF TZP	Homo sapiens (human)	0	1
V5DUJ1	Polyadenylate-binding protein	TCDM_00069	Trypanosoma cruzi Dm28c	0	1
Q8K0C7	Oxysterol-binding protein	Osbp2	Mus musculus (house mouse)	0	1
Q3UHT7	ELKS/RAB6-interacting/CAST family member 2	Erc2 D14Ertd171e	Mus musculus (house mouse)	0	1
Q4DUG1	Clu domain-containing protein	Tc00.1047053508837.80	Trypanosoma cruzi strain CL Brener	0	1
E9QPD7	Pyruvate carboxylase	Pcx	Mus musculus (house mouse)	0	1

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