EuRBPDB

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  • Description
  • RBPome
  • Expression
  • Transcripts
  • Gene Model
  • Phenotypes
  • GWAS
  • PPI
  • Orthologs
  • Gene Ontology
Description
Ensembl ID
ENSG00000054654 (Gene tree)
Gene ID
23224
Gene Symbol
SYNE2
Alias
SYNE-2|DKFZP434H2235|Nesprin-2|NUANCE|NUA|KIAA1011|Nesp2
Full Name
spectrin repeat containing nuclear envelope protein 2
Gene Type
protein_coding
Species
Homo_sapiens
Status
putative
Strand
Plus strand
Length
373,864 bases
Position
chr14:63,852,586-64,226,449
Accession
17084
RBP type
non-canonical RBP
Summary
The protein encoded by this gene is a nuclear outer membrane protein that binds cytoplasmic F-actin. This binding tethers the nucleus to the cytoskeleton and aids in the maintenance of the structural integrity of the nucleus. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009]
RNA binding proteome (RBPome)
PIDTitleMethod TimeAuthorDoi
30607034Comprehensive identification of RNA protein interactions in any organism using orthogonal organic phase separation (OOPS)OOPS & HEK2932019 Jan 3Queiroz RMLDOI: 10.1038/s41587-018-0001-2
30528433The Human RNA-Binding Proteome and Its Dynamics during Translational ArrestXRNAX & HEK2932018 Dec 6Trendel JDOI: 10.1016/j.cell.2018.11.004
30607034Comprehensive identification of RNA protein interactions in any organism using orthogonal organic phase separation (OOPS)OOPS & MCF10A2019 Jan 3Queiroz RMLDOI: 10.1038/s41587-018-0001-2
30528433The Human RNA-Binding Proteome and Its Dynamics during Translational ArrestXRNAX & MCF72018 Dec 6Trendel JDOI: 10.1016/j.cell.2018.11.004
30607034Comprehensive identification of RNA protein interactions in any organism using orthogonal organic phase separation (OOPS)OOPS & U2OS2019 Jan 3Queiroz RMLDOI: 10.1038/s41587-018-0001-2
Expression
Transcripts
Transcript IDNameLengthRefSeq ID Protein IDLengthRefSeq IDUniportKB ID
ENST00000554805SYNE2-2133481--- (aa)--
ENST00000554997SYNE2-215711--- (aa)--
ENST00000557024SYNE2-224998--- (aa)--
ENST00000554584SYNE2-21220508-ENSP000004525706818 (aa)-G3V5X4
ENST00000557005SYNE2-2235804--- (aa)--
ENST00000557060SYNE2-2253203--- (aa)--
ENST00000555002SYNE2-21611532-ENSP000004508313541 (aa)-A0A0C4DGK3
ENST00000555022SYNE2-2173396--- (aa)--
ENST00000557307SYNE2-227526--- (aa)--
ENST00000553289SYNE2-2085261-ENSP00000451184607 (aa)-G3V3D4
ENST00000553801SYNE2-211536-ENSP0000049259016 (aa)-A0A1W2PS37
ENST00000554928SYNE2-2141048--- (aa)--
ENST00000553455SYNE2-210674-ENSP00000452434214 (aa)-G3V5N1
ENST00000553308SYNE2-209557--- (aa)--
ENST00000357395SYNE2-20321555-ENSP000003499696824 (aa)-A0A0A0MRE3
ENST00000341472SYNE2-2011132-ENSP00000344528285 (aa)-Q8WXH0
ENST00000358025SYNE2-20421842XM_005267454ENSP000003507196907 (aa)XP_005267511Q8WXH0
ENST00000556342SYNE2-221572--- (aa)--
ENST00000557084SYNE2-226689-ENSP00000450789199 (aa)-G3V2Q0
ENST00000344113SYNE2-20221777XM_005267458ENSP000003417816885 (aa)XP_005267515Q8WXH0
ENST00000394768SYNE2-20511095--- (aa)--
ENST00000556725SYNE2-222672--- (aa)--
ENST00000555612SYNE2-2206766-ENSP000004519721127 (aa)-G3V4T3
ENST00000458046SYNE2-2072669XM_017021103ENSP00000391937556 (aa)XP_016876592Q8WXH0
ENST00000441438SYNE2-2063084--- (aa)--
ENST00000555323SYNE2-219389--- (aa)--
ENST00000555241SYNE2-218665-ENSP0000049258899 (aa)-A0A1W2PRN9
ENST00000639659SYNE2-2281290-ENSP00000492333429 (aa)-Q8WXH0
Gene Model
Click here to download ENSG00000054654's gene model file
Phenotypes
ensgIDTraitpValuePubmed ID
ENSG00000054654Hemoglobin A, Glycosylated5.6370000E-00519875614
ENSG00000054654Lymphocyte Count9.357e-005-
ENSG00000054654Lymphocyte Count9.631e-005-
ENSG00000054654Lymphocyte Count8.561e-005-
ENSG00000054654Neutrophils4.82e-005-
ENSG00000054654Neutrophils5.818e-005-
ENSG00000054654Neutrophils4.424e-005-
ENSG00000054654Child Development Disorders, Pervasive3.9570000E-007-
ENSG00000054654Child Development Disorders, Pervasive2.8275000E-007-
ENSG00000054654Autistic Disorder4.0461000E-006-
ENSG00000054654Autistic Disorder3.6392000E-006-
ENSG00000054654Child Development Disorders, Pervasive6.9518000E-006-
ENSG00000054654Child Development Disorders, Pervasive2.3881000E-006-
ENSG00000054654Child Development Disorders, Pervasive1.9115000E-005-
ENSG00000054654Autistic Disorder1.5146000E-005-
ENSG00000054654Child Development Disorders, Pervasive8.4024000E-006-
ENSG00000054654Child Development Disorders, Pervasive1.0223000E-005-
ENSG00000054654Child Development Disorders, Pervasive9.7627000E-006-
ENSG00000054654Child Development Disorders, Pervasive1.0578000E-005-
ENSG00000054654Child Development Disorders, Pervasive1.6068000E-005-
ENSG00000054654Child Development Disorders, Pervasive5.5000000E-005-
ENSG00000054654Child Development Disorders, Pervasive4.5000000E-005-
ENSG00000054654Myocardial Infarction2.2360000E-005-
ENSG00000054654Myocardial Infarction1.7400000E-005-
ENSG00000054654Myocardial Infarction2.0030000E-005-
ENSG00000054654Myocardial Infarction1.7960000E-005-
ENSG00000054654Myocardial Infarction2.4020000E-005-
ENSG00000054654Myocardial Infarction2.4230000E-005-
ENSG00000054654Myocardial Infarction2.3310000E-005-
ENSG00000054654Myocardial Infarction1.7630000E-005-
ENSG00000054654Myocardial Infarction2.3890000E-005-
ENSG00000054654Myocardial Infarction1.7950000E-005-
ENSG00000054654Myocardial Infarction1.8200000E-005-
ENSG00000054654Myocardial Infarction1.3620000E-005-
ENSG00000054654Myocardial Infarction2.3430000E-005-
ENSG00000054654Myocardial Infarction2.2750000E-005-
ENSG00000054654Myocardial Infarction1.5100000E-005-
ENSG00000054654Myocardial Infarction2.4590000E-005-
ENSG00000054654Myocardial Infarction1.4340000E-005-
ENSG00000054654Myocardial Infarction1.5170000E-005-
ENSG00000054654Myocardial Infarction2.3260000E-005-
ENSG00000054654Myocardial Infarction1.0810000E-005-
ENSG00000054654Myocardial Infarction9.2370000E-006-
ENSG00000054654Myocardial Infarction2.0770000E-005-
ENSG00000054654Myocardial Infarction2.5970000E-005-
ENSG00000054654Atrial Fibrillation6E-1322544366
GWAS
ensgIDSNPChromosomePositionSNP-risk TraitPubmedID95% CIOr or BEAT EFO ID
ENSG00000054654rs27384131464213242AAtrial fibrillation30061737[1.07-1.10]1.08EFO_0000275
ENSG00000054654rs11525951464208263TEducational attainment (MTAG)30038396[0.0061-0.0111] unit decrease0.0086EFO_0004784
ENSG00000054654rs11525911464214130AAtrial fibrillation28416818[1.06-1.13]1.09EFO_0000275
ENSG00000054654rs27384131464213242AAtrial fibrillation29892015[1.07-1.1]1.08EFO_0000275
ENSG00000054654rs27384131464213242AAtrial fibrillation29892015[1.06-1.1]1.08EFO_0000275
ENSG00000054654rs11525911464214130AAtrial fibrillation22544366[1.09-1.17]1.13EFO_0000275
ENSG00000054654rs9150571464219489GDepression29700475[1.02-1.04]1.0309278EFO_0003761
ENSG00000054654rs23571761463942595?Nevus count or cutaneous melanoma30429480EFO_0004632|EFO_0000389
ENSG00000054654rs108731721463923312GBlond vs. brown/black hair color30531825NR1.068EFO_0003924
ENSG00000054654rs1481142811464160241?Mean corpuscular hemoglobin30595370EFO_0004527
ENSG00000054654rs108731721463923312?Hair color30595370EFO_0007822
Protein-Protein Interaction (PPI)

Clik here to download ENSG00000054654's network

* RBP PPI network refers to all genes directly bind to RBP
Orthologs identified by RBPome
Ensembl IDGene SymbolCoverageIdentiy OrthologGene SymbolCoverageIdentiy Species
ENSG00000054654SYNE210098.990ENSMUSG00000063450Syne210096.396Mus_musculus
Gene Ontology
Go IDGo_termPubmedIDEvidenceCategory
GO:0003779actin binding-ISSFunction
GO:0005515protein binding15671068.18396275.22555292.22632968.23414517.24880667.26506308.IPIFunction
GO:0005634nucleus12118075.IDAComponent
GO:0005635nuclear envelope15671068.IDAComponent
GO:0005640nuclear outer membrane-IEAComponent
GO:0005654nucleoplasm-IEAComponent
GO:0005737cytoplasm12118075.15671068.IDAComponent
GO:0005739mitochondrion15671068.IDAComponent
GO:0005813centrosome21873635.IBAComponent
GO:0005925focal adhesion15671068.IDAComponent
GO:0007097nuclear migration20724637.IMPProcess
GO:0010457centriole-centriole cohesion21873635.IBAProcess
GO:0016021integral component of membrane-IEAComponent
GO:0016235aggresome-IDAComponent
GO:0016529sarcoplasmic reticulum15671068.IDAComponent
GO:0021817nucleokinesis involved in cell motility in cerebral cortex radial glia guided migration-IEAProcess
GO:0030018Z disc15671068.IDAComponent
GO:0030335positive regulation of cell migration-ISSProcess
GO:0031022nuclear migration along microfilament-ISSProcess
GO:0031258lamellipodium membrane15671068.IDAComponent
GO:0031527filopodium membrane15671068.IDAComponent
GO:0031965nuclear membrane-IDAComponent
GO:0031981nuclear lumen15671068.IDAComponent
GO:0033017sarcoplasmic reticulum membrane-IEAComponent
GO:0034993meiotic nuclear membrane microtubule tethering complex18396275.IDAComponent
GO:0045111intermediate filament cytoskeleton-IDAComponent
GO:0051015actin filament binding-IEAFunction
GO:0051642centrosome localization20724637.IMPProcess
GO:0070062extracellular exosome18570454.HDAComponent
GO:0090286cytoskeletal anchoring at nuclear membrane18396275.IDAProcess
GO:1902017regulation of cilium assembly-IEAProcess

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