ENSG00000102580


Homo sapiens

Features
Gene ID: ENSG00000102580
  
Biological name :DNAJC3
  
Synonyms : DNAJC3 / DnaJ heat shock protein family (Hsp40) member C3 / Q13217
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 13
Strand: 1
Band: q32.1
Gene start: 95677139
Gene end: 95794989
  
Corresponding Affymetrix probe sets: 1558080_s_at (Human Genome U133 Plus 2.0 Array)   208499_s_at (Human Genome U133 Plus 2.0 Array)   225284_at (Human Genome U133 Plus 2.0 Array)   235341_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000473631
Ensembl peptide - ENSP00000365991
NCBI entrez gene - 5611     See in Manteia.
OMIM - 601184
RefSeq - XM_017020674
RefSeq - NM_006260
RefSeq - XM_011521104
RefSeq - XM_011521105
RefSeq Peptide - NP_006251
swissprot - X6R9L0
swissprot - A8KA82
swissprot - Q13217
Ensembl - ENSG00000102580
  
Related genetic diseases (OMIM): 616192 - ?Ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus, 616192
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
 dnajc3aENSDARG00000041110Danio rerio
 DNAJC3ENSGALG00000016894Gallus gallus
 Dnajc3ENSMUSG00000022136Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
DNAJC7 / Q99615 / DnaJ heat shock protein family (Hsp40) member C7ENSG0000016825926


Protein motifs (from Interpro)
Interpro ID Name
 IPR001623  DnaJ domain
 IPR011990  Tetratricopeptide-like helical domain superfamily
 IPR013026  Tetratricopeptide repeat-containing domain
 IPR018704  Tetratricopeptide repeat-like domain
 IPR019734  Tetratricopeptide repeat
 IPR036869  Chaperone J-domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006417 regulation of translation IEA
 biological_processGO:0006469 negative regulation of protein kinase activity IEA
 biological_processGO:0006986 response to unfolded protein IEA
 biological_processGO:0036494 positive regulation of translation initiation in response to endoplasmic reticulum stress ISS
 biological_processGO:0036498 IRE1-mediated unfolded protein response TAS
 biological_processGO:0043066 negative regulation of apoptotic process IMP
 biological_processGO:0043312 neutrophil degranulation TAS
 biological_processGO:0043687 post-translational protein modification TAS
 biological_processGO:0044267 cellular protein metabolic process TAS
 biological_processGO:0051603 proteolysis involved in cellular protein catabolic process IEA
 biological_processGO:0051607 defense response to virus IEA
 biological_processGO:0070417 cellular response to cold ISS
 biological_processGO:1903912 negative regulation of endoplasmic reticulum stress-induced eIF2 alpha phosphorylation ISS
 cellular_componentGO:0005576 extracellular region TAS
 cellular_componentGO:0005737 cytoplasm TAS
 cellular_componentGO:0005783 endoplasmic reticulum ISS
 cellular_componentGO:0005788 endoplasmic reticulum lumen TAS
 cellular_componentGO:0005790 smooth endoplasmic reticulum IEA
 cellular_componentGO:0005829 cytosol IEA
 cellular_componentGO:0016020 membrane HDA
 cellular_componentGO:0031205 endoplasmic reticulum Sec complex IEA
 cellular_componentGO:0035578 azurophil granule lumen TAS
 cellular_componentGO:0070062 extracellular exosome HDA
 cellular_componentGO:1903561 extracellular vesicle HDA
 molecular_functionGO:0004860 protein kinase inhibitor activity TAS
 molecular_functionGO:0005515 protein binding IEA
 molecular_functionGO:0019901 protein kinase binding IEA
 molecular_functionGO:0051087 chaperone binding IEA
 molecular_functionGO:0051787 misfolded protein binding IEA


Pathways (from Reactome)
Pathway description
Viral mRNA Translation
XBP1(S) activates chaperone genes
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)
Neutrophil degranulation
Post-translational protein phosphorylation


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:0000407 Hearing loss, sensorineural "Hearing loss caused by damage or dysfunction of the auditory nerve (cranial nerve VIII)." [HPO:curators]
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 HP:0000819 Diabetes mellitus 
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 HP:0001256 Mental retardation, mild "Mild mental retardation is defined as an intelligence quotient (IQ) in the range of 50-69." [HPO:curators]
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 HP:0001272 Cerebellar atrophy 
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 HP:0002059 Cerebral atrophy 
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 HP:0002066 Gait ataxia "Impairment of the ability to coordinate the movements required for normal walking." [HPO:curators]
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 HP:0002522 Areflexia in lower limbs 
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 HP:0003487 Babinski sign "Upturning of the big toe (and sometimes fanning of the other toes) in response to stimulation of the sole of the foot. If the Babinski sign is present it can indicate damage to the corticospinal tract." [HPO:curators]
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 HP:0004322 Decreased body height "A height below that which is expected according to age and gender norms. Although there is no universally accepted definition of short stature, many refer to "short stature" as height more than 2 standard deviations below the mean for age and gender (or below the 3rd percentile for age and gender dependent norms)." [HPO:curators]
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 HP:0004325 Decreased body weight 
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 HP:0006827 MRI shows atrophy of the spinal cord 
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 HP:0007108 Demyelinating peripheral neuropathy 
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 HP:0007141 Sensorimotor neuropathy 
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 HP:0007366 Atrophy/Degeneration affecting the brainstem 
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 HP:0008619 Hearing loss, sensorineural, bilateral 
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 HP:0010871 Sensory ataxia "Incoordination of movement caused by a deficit in the sensory nervous system. Sensory ataxia can be distinguished from cerebellar ataxia by asking the patient to close his or her eyes. Persons with cerebellar ataxia show only a minimal worsening of symptoms, whereas persons with sensory ataxia show a marked worsening of symptoms." [HPO:probinson]
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 HP:0100543 Cognitive impairment "Abnormality in the process of thought including the ability to process information." [HPO:sdoelken]
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 HP:0100651 Diabetes mellitus Type I 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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