ENSG00000101327


Homo sapiens

Features
Gene ID: ENSG00000101327
  
Biological name :PDYN
  
Synonyms : P01213 / PDYN / prodynorphin
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 20
Strand: -1
Band: p13
Gene start: 1978757
Gene end: 1994285
  
Corresponding Affymetrix probe sets: 206803_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000217305
Ensembl peptide - ENSP00000440185
Ensembl peptide - ENSP00000442259
NCBI entrez gene - 5173     See in Manteia.
OMIM - 131340
RefSeq - NM_024411
RefSeq - XM_017027878
RefSeq - NM_001190892
RefSeq - NM_001190898
RefSeq - NM_001190899
RefSeq - NM_001190900
RefSeq - XM_011529245
RefSeq - XM_011529246
RefSeq - XM_011529247
RefSeq - XM_011529248
RefSeq - XM_011529249
RefSeq - XM_011529250
RefSeq - XM_011529244
RefSeq Peptide - NP_001177827
RefSeq Peptide - NP_001177828
RefSeq Peptide - NP_001177829
RefSeq Peptide - NP_077722
RefSeq Peptide - NP_001177821
swissprot - P01213
Ensembl - ENSG00000101327
  
Related genetic diseases (OMIM): 610245 - Spinocerebellar ataxia 23, 610245
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
 pdynENSDARG00000087798Danio rerio
 PDYNENSGALG00000027211Gallus gallus
 PdynENSMUSG00000027400Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
PENK / P01210 / proenkephalinENSG0000018119530


Protein motifs (from Interpro)
Interpro ID Name
 IPR000750  Proenkephalin B
 IPR006024  Opioid neuropeptide precursor


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007186 G-protein coupled receptor signaling pathway TAS
 biological_processGO:0007218 neuropeptide signaling pathway IBA
 biological_processGO:0007268 chemical synaptic transmission IBA
 biological_processGO:0007600 sensory perception IBA
 biological_processGO:0010469 regulation of signaling receptor activity IEA
 cellular_componentGO:0005576 extracellular region TAS
 cellular_componentGO:0005886 plasma membrane IDA
 cellular_componentGO:0030425 dendrite IBA
 cellular_componentGO:0043025 neuronal cell body IBA
 cellular_componentGO:0043679 axon terminus IBA
 molecular_functionGO:0001515 opioid peptide activity IEA
 molecular_functionGO:0005184 neuropeptide hormone activity IBA
 molecular_functionGO:0031628 opioid receptor binding IBA


Pathways (from Reactome)
Pathway description
Opioid Signalling
G-protein activation
Peptide ligand-binding receptors
G alpha (i) signalling events


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:0000514 Slow saccades 
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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:0001272 Cerebellar atrophy 
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 HP:0001274 Agenesis of corpus callosum "Absence of the corpus callosum as a result of the failure of the corpus callosum to develop, which can be the result of a failure in any one of the multiple steps of callosal development including cellular proliferation and migration, axonal growth or glial patterning at the midline." [HPO:curators]
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 HP:0001310 Dysmetria 
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 HP:0001337 Tremor "An unintentional, oscillating to-and-fro muscle movement." [HPO:curators]
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 HP:0001347 Hyperreflexia "The presence of overactive or overresponsive reflexes." [HPO:curators]
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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:0002070 Limb ataxia 
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 HP:0002073 Progressive cerebellar ataxia 
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 HP:0002166 Decreased vibratory sense in the lower limbs "A decrease in the ability to perceive vibration in the legs." [HPO:curators]
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 HP:0002529 Neuropathology shows neuronal loss in basal ganglia, brainstem, and cerebellum 
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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:0003677 Slow progression 
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 HP:0006886 Decreased distal vibration sense "A decrease in the ability to perceive vibration in the distal portions of the limbs." [HPO:curators]
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 HP:0007141 Sensorimotor neuropathy 
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 HP:0007305 Cns demyelination 
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 HP:0010831 Impaired proprioception "A loss or impairment of the sensation of the relative position of parts of the body and joint position." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000112038 OPRM1 / P35372 / opioid receptor mu 1  / complex / reaction
 ENSG00000186469 GNG2 / P59768 / G protein subunit gamma 2  / reaction / complex
 ENSG00000078369 GNB1 / P62873 / G protein subunit beta 1  / reaction / complex






 

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