ENSG00000116675


Homo sapiens

Features
Gene ID: ENSG00000116675
  
Biological name :DNAJC6
  
Synonyms : DNAJC6 / DnaJ heat shock protein family (Hsp40) member C6 / O75061
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 1
Strand: 1
Band: p31.3
Gene start: 65248219
Gene end: 65415869
  
Corresponding Affymetrix probe sets: 204720_s_at (Human Genome U133 Plus 2.0 Array)   204721_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000263441
Ensembl peptide - ENSP00000360108
Ensembl peptide - ENSP00000378735
Ensembl peptide - ENSP00000473821
NCBI entrez gene - 9829     See in Manteia.
OMIM - 608375
RefSeq - NM_001256865
RefSeq - NM_001256864
RefSeq - NM_014787
RefSeq Peptide - NP_001243793
RefSeq Peptide - NP_001243794
RefSeq Peptide - NP_055602
swissprot - O75061
swissprot - S4R305
Ensembl - ENSG00000116675
  
Related genetic diseases (OMIM): 615528 - Parkinson disease 19a, juvenile-onset, 615528
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
 dnajc6ENSDARG00000079891Danio rerio
 DNAJC6ENSGALG00000011041Gallus gallus
 Dnajc6ENSMUSG00000028528Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
GAK / O14976 / cyclin G associated kinaseENSG0000017895046
TNS3 / Q68CZ2 / tensin 3ENSG0000013620520
TNS1 / Q9HBL0 / tensin 1ENSG0000007930819
TNS2 / Q63HR2 / tensin 2ENSG0000011107718
TPTE2 / Q6XPS3 / transmembrane phosphoinositide 3-phosphatase and tensin homolog 2ENSG000001329589
TNS4 / Q8IZW8 / tensin 4ENSG000001317469
TPTE / P56180 / transmembrane phosphatase with tensin homologyENSG000002743918
PTEN / P60484 / phosphatase and tensin homologENSG000001718628


Protein motifs (from Interpro)
Interpro ID Name
 IPR001623  DnaJ domain
 IPR014020  Tensin phosphatase, C2 domain
 IPR029021  Protein-tyrosine phosphatase-like
 IPR029023  Tensin-type phosphatase domain
 IPR035892  C2 domain superfamily
 IPR036869  Chaperone J-domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006470 protein dephosphorylation IEA
 biological_processGO:0006898 receptor-mediated endocytosis IBA
 biological_processGO:0016191 synaptic vesicle uncoating ISS
 biological_processGO:0035335 peptidyl-tyrosine dephosphorylation IEA
 biological_processGO:0061024 membrane organization TAS
 biological_processGO:0072318 clathrin coat disassembly IEA
 biological_processGO:2000369 regulation of clathrin-dependent endocytosis IEA
 cellular_componentGO:0005829 cytosol TAS
 cellular_componentGO:0014069 postsynaptic density IEA
 cellular_componentGO:0031982 vesicle IBA
 cellular_componentGO:0045202 synapse IEA
 molecular_functionGO:0004721 phosphoprotein phosphatase activity IEA
 molecular_functionGO:0004725 protein tyrosine phosphatase activity IEA
 molecular_functionGO:0016787 hydrolase activity IEA
 molecular_functionGO:0017124 SH3 domain binding IEA


Pathways (from Reactome)
Pathway description
Lysosome Vesicle Biogenesis
Golgi Associated Vesicle Biogenesis
Clathrin-mediated endocytosis


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:0000338 Hypomimic face 
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 HP:0000571 Hypometric saccades 
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 HP:0000738 Hallucinations 
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 HP:0001249 Mental retardation 
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 HP:0001250 Seizures "Seizures are an intermittent `abnormality of the central nervous system` (FMA:HP:0002011) due to a sudden, excessive, disorderly discharge of cerebral neurons and characterized clinically by some combination of disturbance of sensation, loss of consciousness, impairment of psychic function, or convulsive movements." [HPO:probinson]
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 HP:0001257 Spasticity "A motor disorder characterized by a velocity-dependent increase in tonic stretch reflexes with increased muscle tone, exaggerated (hyperexcitable) tendon reflexes." [HPO:curators]
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 HP:0001260 Dysarthria "Dysarthric speech is a general description referring to a neurological speech disorder characterized by poor articulation. Depending on the involved neurological structures, dysarthria may be further classified as spastic, flaccid, ataxic, hyperkinetic and hypokinetic, or mixed." [HPO:curators]
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 HP:0001265 Hyporeflexia 
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 HP:0001300 Parkinsonism 
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 HP:0001332 Dystonia "An abnormally increased muscular tone that causes fixed abnormal postures. There is a slow, intermittent twisting motion that leads to exaggerated turning and posture of the extremities and trunk." [HPO:curators]
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 HP:0001336 Myoclonus "Very brief, involuntary random muscular contractions occurring at rest, in response to sensory stimuli, or accompanying voluntary movements." [HPO:curators]
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 HP:0001337 Tremor "An unintentional, oscillating to-and-fro muscle movement." [HPO:curators]
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 HP:0001621 Soft voice 
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 HP:0001761 Pes cavus 
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 HP:0002063 Rigidity 
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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:0002067 Bradykinesia "Bradykinesia literally means slow movement, and is used clinically to denote a slowness in the execution of movement (in contrast to hypokinesia, which is used to refer to slowness in the initiation of movement)." [HPO:curators]
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 HP:0002172 Postural instability 
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 HP:0002304 Akinesia 
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 HP:0002322 Resting tremor "A resting tremor occurs when muscles are at rest and becomes less noticeable or disappears when the affected muscles are moved. Resting tremors are often slow and coarse." [HPO:curators]
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 HP:0002362 Shuffling gait 
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 HP:0002425 Anarthria "A defect in the motor ability that enables speech." [HPO:curators]
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 HP:0002540 Inability to walk 
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 HP:0002650 Scoliosis "The presence of an abnormal lateral curvature of the spine." [HPO:curators]
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 HP:0003677 Slow progression 
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 HP:0003678 Rapidly progressive 
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 HP:0007164 Slowed slurred speech 
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 HP:0007256 Mild pyramidal signs 
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 HP:0007311 Short stepped shuffling gait 
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 HP:0008969 Leg muscle stiffness 
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 HP:0012378 Fatigue "A subjective feeling of tiredness characterized by a lack of energy and motivation." [HPO:probinson]
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 HP:0012444 Brain atrophy "Partial or complete wasting (loss) of brain tissue that was once present." [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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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000109971 HSPA8 / P11142 / heat shock protein family A (Hsp70) member 8  / complex






 

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