ENSG00000134769


Homo sapiens

Features
Gene ID: ENSG00000134769
  
Biological name :DTNA
  
Synonyms : DTNA / dystrobrevin alpha / Q9Y4J8
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 18
Strand: 1
Band: q12.1
Gene start: 34493290
Gene end: 34891844
  
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: Ensembl peptide - ENSP00000473078
Ensembl peptide - ENSP00000472031
Ensembl peptide - ENSP00000473119
Ensembl peptide - ENSP00000269192
Ensembl peptide - ENSP00000283365
Ensembl peptide - ENSP00000322519
Ensembl peptide - ENSP00000336682
Ensembl peptide - ENSP00000382064
Ensembl peptide - ENSP00000382072
Ensembl peptide - ENSP00000405819
Ensembl peptide - ENSP00000451516
Ensembl peptide - ENSP00000452255
Ensembl peptide - ENSP00000464904
Ensembl peptide - ENSP00000465063
Ensembl peptide - ENSP00000466573
Ensembl peptide - ENSP00000466978
Ensembl peptide - ENSP00000467720
Ensembl peptide - ENSP00000468138
Ensembl peptide - ENSP00000468262
Ensembl peptide - ENSP00000468473
Ensembl peptide - ENSP00000468631
Ensembl peptide - ENSP00000469121
Ensembl peptide - ENSP00000470152
Ensembl peptide - ENSP00000470247
Ensembl peptide - ENSP00000470716
Ensembl peptide - ENSP00000470934
Ensembl peptide - ENSP00000471143
Ensembl peptide - ENSP00000471783
NCBI entrez gene - 1837     See in Manteia.
OMIM - 601239
RefSeq - XM_017025602
RefSeq - NM_032981
RefSeq - XM_005258221
RefSeq - XM_011525853
RefSeq - XM_017025575
RefSeq - XM_017025576
RefSeq - XM_017025577
RefSeq - XM_017025578
RefSeq - XM_017025579
RefSeq - XM_017025580
RefSeq - XM_017025581
RefSeq - XM_017025582
RefSeq - XM_017025583
RefSeq - XM_017025584
RefSeq - XM_017025585
RefSeq - XM_017025586
RefSeq - XM_017025587
RefSeq - XM_017025588
RefSeq - XM_017025589
RefSeq - XM_017025590
RefSeq - XM_017025591
RefSeq - XM_017025592
RefSeq - XM_017025593
RefSeq - XM_017025594
RefSeq - XM_017025595
RefSeq - XM_017025596
RefSeq - XM_017025597
RefSeq - XM_017025598
RefSeq - XM_017025599
RefSeq - XM_017025600
RefSeq - XM_017025601
RefSeq - NM_001128175
RefSeq - NM_001198938
RefSeq - NM_001198939
RefSeq - NM_001198940
RefSeq - NM_001198941
RefSeq - NM_001198942
RefSeq - NM_001198943
RefSeq - NM_001198944
RefSeq - NM_001198945
RefSeq - NM_001390
RefSeq - NM_001391
RefSeq - NM_001392
RefSeq - NM_032975
RefSeq - NM_032978
RefSeq - NM_032979
RefSeq - NM_032980
RefSeq Peptide - NP_001185867
RefSeq Peptide - NP_001185871
RefSeq Peptide - NP_001185872
RefSeq Peptide - NP_001185873
RefSeq Peptide - NP_001185874
RefSeq Peptide - NP_001381
RefSeq Peptide - NP_001382
RefSeq Peptide - NP_001383
RefSeq Peptide - NP_116757
RefSeq Peptide - NP_116760
RefSeq Peptide - NP_116761
RefSeq Peptide - NP_116762
RefSeq Peptide - NP_116763
RefSeq Peptide - NP_001121647
RefSeq Peptide - NP_001185868
RefSeq Peptide - NP_001185869
RefSeq Peptide - NP_001185870
swissprot - K7EJ84
swissprot - K7EMN1
swissprot - K7ENJ7
swissprot - K7ER73
swissprot - K7ERH7
swissprot - K7ERZ2
swissprot - K7ESB2
swissprot - M0QZ28
swissprot - M0R021
swissprot - M0R0C4
swissprot - Q9Y4J8
swissprot - A0A024RC32
swissprot - K7EIV1
Ensembl - ENSG00000134769
  
Related genetic diseases (OMIM): 604169 - Left ventricular noncompaction 1, with or without congenital heart defects, 604169
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 dtnaENSDARG00000031015Danio rerio
 DTNAENSGALG00000015211Gallus gallus
 DtnaENSMUSG00000024302Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
DTNB / O60941 / dystrobrevin betaENSG0000013810162
DMD / P11532 / dystrophinENSG0000019894724
UTRN / P46939 / utrophinENSG0000015281823
DRP2 / Q13474 / dystrophin related protein 2ENSG0000010238522
DYTN / A2CJ06 / dystrotelinENSG0000023212516


Protein motifs (from Interpro)
Interpro ID Name
 IPR000433  Zinc finger, ZZ-type
 IPR011992  EF-hand domain pair
 IPR015153  EF-hand domain, type 1
 IPR015154  EF-hand domain, type 2
 IPR017432  Distrobrevin


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:0005886 plasma membrane IEA
 cellular_componentGO:0016020 membrane 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:0042995 cell projection 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
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000006 Autosomal dominant inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators]
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 HP:0001629 Ventricular septal defect "A hole between the two bottom chambers (ventricles) of the heart. The defect is centered around the most superior aspect of the ventricular septum." [HPO:curators]
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 HP:0001635 Congestive heart failure "The presence of an abnormality of cardiac function that is responsible for the failure of the heart to pump blood at a rate that is commensurate with the needs of the tissues or a state in which abnormally elevated filling pressures are required for the heart to do so. Heart failure is frequently related to a defect in myocardial contraction." [HPO:curators]
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 HP:0001643 Patent ductus arteriosus 
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 HP:0001645 Sudden cardiac death 
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 HP:0001653 Mitral regurgitation "An `abnormality of the mitral valve` (HP:0001633) characterized by insufficiency or incompetence of the mitral valve resulting in retrograde leaking of blood through the mitral valve upon ventricular contraction." [HPO:probinson]
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 HP:0001712 Left ventricular hypertrophy 
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 HP:0004308 Ventricular arrhythmia 
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 HP:0004383 Hypoplastic left heart 
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 HP:0005110 Atrial fibrillation 
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 HP:0011664 Non-compaction cardiomyopathy "Left ventricular non-compaction (LVNC) is characterized by prominent left ventricular trabeculae and deep inter-trabecular recesses. The myocardial wall is often thickened with a thin, compacted epicardial layer and a thickened endocardial layer. In some patients, LVNC is associated with left ventricular dilatation and systolic dysfunction, which can be transient in neonates." [pmid:17916581]
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 HP:0030682 Left ventricular noncompaction "Left ventricular noncompaction (LVNC) is defined by 3 markers: prominent left ventricular (LV) trabeculae, deep intertrabecular recesses, and the thin compacted layer." [PMID:16670098, PMID:25443708]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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