1837


Homo sapiens (NCBI)

Features
Gene ID: 1837
  
Biological name :
  
Synonyms : D18S892E|DRP3|DTN|DTN-A|LVNC1 / DTNA / dystrobrevin alpha
  
Possible biological names infered from orthology :
  
Species: Homo sapiens (NCBI)
  
Chr. number:
Strand:
Band:
Gene start:
Gene end:
  
Corresponding Affymetrix probe sets: 205741_s_at (Human Genome U133 Plus 2.0 Array)   208430_s_at (Human Genome U133 Plus 2.0 Array)   210091_s_at (Human Genome U133 Plus 2.0 Array)   210611_s_at (Human Genome U133 Plus 2.0 Array)   210736_x_at (Human Genome U133 Plus 2.0 Array)   211493_x_at (Human Genome U133 Plus 2.0 Array)   227084_at (Human Genome U133 Plus 2.0 Array)   244142_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: RefSeq - 42717994
RefSeq - 1034603506
RefSeq - 1034603508
RefSeq - 1034603511
RefSeq - 1034603513
RefSeq - 1034603515
RefSeq - 1034603517
RefSeq - 1034603519
RefSeq - 1034603523
RefSeq - 1034603525
RefSeq - 1034603527
RefSeq - 1034603529
RefSeq - 1034603531
RefSeq - 1034603533
RefSeq - 1034603535
RefSeq - 1034603537
RefSeq - 1034603541
RefSeq - 1034603543
RefSeq - 1034603545
RefSeq - 1034603550
RefSeq - 1034603552
RefSeq - 1034603554
RefSeq - 1034603556
RefSeq - 1034603558
RefSeq - 1034603560
RefSeq - 1370473145
RefSeq - 1370473152
RefSeq - 1370473164
RefSeq - 14916515
RefSeq - 189571587
RefSeq - 312147255
RefSeq - 312147259
RefSeq - 312147263
RefSeq - 312147269
RefSeq - 312147274
RefSeq - 312147278
RefSeq - 312147282
RefSeq - 312147286
RefSeq - 1034603504
RefSeq - 42717997
RefSeq - 42717999
RefSeq - 42718001
RefSeq - 42718003
RefSeq - 42718005
RefSeq - 42718007
RefSeq - 530413697
RefSeq - 767998351
RefSeq - NC_000018.10
RefSeq - NG_009201.1
RefSeq - NP_001121647.1
RefSeq - NP_001185867.1
RefSeq - NP_001185868.1
RefSeq - NP_001185869.1
RefSeq - NP_001185870.1
RefSeq - NP_001185871.1
RefSeq - NP_001185872.1
RefSeq - NP_001185873.1
RefSeq - NP_001185874.1
RefSeq - NP_001381.2
RefSeq - NP_001382.2
RefSeq - NP_001383.2
RefSeq - NP_116757.2
RefSeq - NP_116760.2
RefSeq - NP_116761.2
RefSeq - NP_116762.2
RefSeq - NP_116763.1
RefSeq - XP_005258278.1
RefSeq - XP_011524155.1
RefSeq - XP_016881064.1
RefSeq - XP_016881065.1
RefSeq - XP_016881066.1
RefSeq - XP_016881067.1
RefSeq - XP_016881068.1
RefSeq - XP_016881069.1
RefSeq - XP_016881070.1
RefSeq - XP_016881071.1
RefSeq - XP_016881073.1
RefSeq - XP_016881074.1
RefSeq - XP_016881075.1
RefSeq - XP_016881076.1
RefSeq - XP_016881077.1
RefSeq - XP_016881078.1
RefSeq - XP_016881079.1
RefSeq - XP_016881080.1
RefSeq - XP_016881082.1
RefSeq - XP_016881083.1
RefSeq - XP_016881084.1
RefSeq - XP_016881086.1
RefSeq - XP_016881087.1
RefSeq - XP_016881088.1
RefSeq - XP_016881089.1
RefSeq - XP_016881090.1
RefSeq - XP_016881091.1
RefSeq - XP_024306864.1
RefSeq - XP_024306865.1
RefSeq - XP_024306866.1
RefSeq - XM_017025587.2
RefSeq - XM_017025588.2
RefSeq - XM_017025589.2
RefSeq - XM_017025590.2
RefSeq - XM_017025591.2
RefSeq - XM_017025593.2
RefSeq - XM_017025594.2
RefSeq - XM_017025595.1
RefSeq - XM_017025597.2
RefSeq - XM_017025598.2
RefSeq - XM_017025599.2
RefSeq - XM_017025600.2
RefSeq - XM_017025601.2
RefSeq - NM_001128175.1
RefSeq - NM_001198938.1
RefSeq - NM_001198939.1
RefSeq - NM_001198940.1
RefSeq - NM_001198941.1
RefSeq - NM_001198942.1
RefSeq - NM_001198943.1
RefSeq - NM_001198944.1
RefSeq - NM_001198945.1
RefSeq - NM_001390.4
RefSeq - NM_001391.5
RefSeq - NM_001392.4
RefSeq - NM_032975.3
RefSeq - NM_032978.6
RefSeq - NM_032979.4
RefSeq - NM_032980.3
RefSeq - NM_032981.4
RefSeq - XM_017025602.2
RefSeq - XM_024451096.1
RefSeq - XM_024451097.1
RefSeq - XM_024451098.1
RefSeq - XR_001753161.1
RefSeq - XR_001753162.1
RefSeq - XR_001753163.1
RefSeq - XR_002958166.1
RefSeq - XR_001753152.1
RefSeq - XR_001753153.1
RefSeq - XR_001753154.1
RefSeq - XR_001753155.1
RefSeq - XR_001753156.1
RefSeq - XR_001753157.1
RefSeq - XR_001753158.1
RefSeq - XR_001753159.1
RefSeq - XR_001753160.1
RefSeq - XM_005258221.5
RefSeq - XM_011525853.3
RefSeq - XM_017025575.2
RefSeq - XM_017025576.2
RefSeq - XM_017025577.2
RefSeq - XM_017025578.2
RefSeq - XM_017025579.2
RefSeq - XM_017025580.1
RefSeq - XM_017025581.2
RefSeq - XM_017025582.2
RefSeq - XM_017025584.2
RefSeq - XM_017025585.2
RefSeq - XM_017025586.2
  
See co-cited genes in PubMed
Warning: Please see the Ensembl gene model ENSG00000134769 to get all the annotations available for this gene.


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006941 striated muscle contraction TAS
 biological_processGO:0007165 signal transduction TAS
 biological_processGO:0007268 chemical synaptic transmission TAS
 biological_processGO:0007274 neuromuscular synaptic transmission TAS
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0030054 cell junction IEA
 cellular_componentGO:0030424 axon IEA
 cellular_componentGO:0031234 extrinsic component of cytoplasmic side of plasma membrane IEA
 cellular_componentGO:0032991 protein-containing complex IDA
 cellular_componentGO:0042383 sarcolemma IEA
 cellular_componentGO:0045202 synapse IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0008270 zinc ion binding IEA
 molecular_functionGO:0030165 PDZ domain binding IEA


Pathways (from Reactome)
Pathway description
No match


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

1 s.

 
External programs and data are copyrighted by and are the property of their respective authors.
The Manteia system, data and analyses are provided "as is" with no warranties, expressed or implied as to capabilities or accuracy. User assumes the entire risk as to the results and performance of the software, data and documentation


                   


© Olivier Tassy / Olivier Pourquie 2007-2024
contact: otassy@igbmc.fr