ENSG00000187726


Homo sapiens

Features
Gene ID: ENSG00000187726
  
Biological name :DNAJB13
  
Synonyms : DNAJB13 / DnaJ heat shock protein family (Hsp40) member B13 / P59910
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 11
Strand: 1
Band: q13.4
Gene start: 73950319
Gene end: 73970366
  
Corresponding Affymetrix probe sets: 230936_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000344431
Ensembl peptide - ENSP00000438576
Ensembl peptide - ENSP00000439711
Ensembl peptide - ENSP00000440778
NCBI entrez gene - 374407     See in Manteia.
OMIM - 610263
RefSeq - XM_017017678
RefSeq - NM_153614
RefSeq - XM_017017675
RefSeq - XM_017017676
RefSeq - XM_017017677
RefSeq - XM_005273984
RefSeq - XM_011545004
RefSeq - XM_011545005
RefSeq - XM_011545007
RefSeq - XM_011545009
RefSeq - XM_011545015
RefSeq Peptide - NP_705842
swissprot - P59910
swissprot - H0YFX2
Ensembl - ENSG00000187726
  
Related genetic diseases (OMIM): 617091 - Ciliary dyskinesia, primary, 34, 617091
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
 dnajb13ENSDARG00000043157Danio rerio
 DNAJB13ENSGALG00000017317Gallus gallus
 Q80Y75ENSMUSG00000030708Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
DNAJB1 / P25685 / DnaJ heat shock protein family (Hsp40) member B1ENSG0000013200251
DNAJB5 / O75953 / DnaJ heat shock protein family (Hsp40) member B5ENSG0000013709450
DNAJB4 / Q9UDY4 / DnaJ heat shock protein family (Hsp40) member B4ENSG0000016261648
DNAJB6 / O75190 / DnaJ heat shock protein family (Hsp40) member B6ENSG0000010599327
DNAJB8 / Q8NHS0 / DnaJ heat shock protein family (Hsp40) member B8ENSG0000017940721
DNAJB7 / Q7Z6W7 / DnaJ heat shock protein family (Hsp40) member B7ENSG0000017240421
DNAJB2 / P25686 / DnaJ heat shock protein family (Hsp40) member B2ENSG0000013592420
DNAJB9 / Q9UBS3 / DnaJ heat shock protein family (Hsp40) member B9ENSG0000012859017


Protein motifs (from Interpro)
Interpro ID Name
 IPR001623  DnaJ domain
 IPR002939  Chaperone DnaJ, C-terminal
 IPR008971  HSP40/DnaJ peptide-binding
 IPR018253  DnaJ domain, conserved site
 IPR036869  Chaperone J-domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006457 protein folding IEA
 biological_processGO:0030030 cell projection organization IEA
 biological_processGO:1904158 axonemal central apparatus assembly IMP
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005929 cilium IEA
 cellular_componentGO:0005930 axoneme IEA
 cellular_componentGO:0031514 motile cilium IEA
 cellular_componentGO:0036126 sperm flagellum IDA
 cellular_componentGO:0042995 cell projection IEA
 cellular_componentGO:0097224 sperm connecting piece ISS
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0051082 unfolded protein binding IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive 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 homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0002205 Recurrent respiratory infections 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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