PDYN - prodynorphin Gene
Also Known as ADCA; PENKB; SCA23
Species: Homo sapiens
About PDYN
This gene has 11 transcripts (splice variants), 188 orthologues, 2 paralogues and is associated with 2 phenotypes. Restricted expression toward brain (RPKM 14.6).
Summary
The protein encoded by this gene is a preproprotein that is proteolytically processed to form the secreted opioid peptides beta-neoendorphin, dynorphin, leu-enkephalin, rimorphin, and leumorphin. These peptides are ligands for the kappa-type of Opioid Receptor. Dynorphin is involved in modulating responses to several psychoactive substances, including cocaine. Multiple alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2010]
PDYN Products (5)
| mRNA | Protein | Name |
|---|---|---|
| NM_001190892.1 | NP_001177821.1 | proenkephalin-B preproprotein |
| NM_001190898.3 | NP_001177827.1 | proenkephalin-B preproprotein |
| NM_001190899.2 | NP_001177828.1 | proenkephalin-B preproprotein |
| NM_001190900.1 | NP_001177829.1 | proenkephalin-B preproprotein |
| NM_024411.5 | NP_077722.1 | proenkephalin-B preproprotein |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
28514442 | GOA |
| Cellular Component GO Annotation | Evidence | References | Source |
|---|---|---|---|
| is active in hippocampal mossy fiber to CA3 synapse |
IDA
IDA: Inferred from direct assay
|
10098940 | GOA |
| is active in neuronal dense core vesicle |
IDA
IDA: Inferred from direct assay
|
10098940 | GOA |
| located in plasma membrane |
IDA
IDA: Inferred from direct assay
|
9047294 | GOA |
PDYN Protein Structure
Opiods_neuropep: Vertebrate endogenous opioids neuropeptide (21 - 68)
- 0
- 100
- 200
- 254 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
proenkephalin-B |
|
Recombinant PDYN Proteins
| Cat. No. | Product Name | Accession | Purity |
|---|---|---|---|
| HY-P71058 | PDYN Protein, Human (HEK293, His) | P01213 (D21-A254) | ≥ 95%, as determined by reducing SDS-PAGE. |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Spinocerebellar Ataxia 23 |
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| Cocaine Dependence |
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| Drug Dependence |
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| Temporal Lobe Epilepsy |
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| Opiate Dependence |
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| Heroin Dependence |
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| Pain Agnosia |
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| Opioid Abuse |
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| Obsessive-Compulsive Disorder |
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| Agnosia |
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| Amnestic Disorder |
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| Withdrawal Disorder |
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| Alcohol Dependence |
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| Spinocerebellar Ataxia, Autosomal Recessive 23 |
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| Narcolepsy |
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| Constipation |
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| Morphine Dependence |
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| Focal Epilepsy |
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| Femoral Cancer |
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| Substance Dependence |
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| Cocaine Abuse |
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| Pheochromocytoma |
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| Specific Developmental Disorder |
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| Parkinson Disease, Late-Onset |
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| Epilepsy |
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| Neonatal Abstinence Syndrome |
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| Amphetamine Abuse |
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| Central Precocious Puberty |
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| Anxiety |
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| Huntington Disease |
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| Bipolar Disorder |
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| Substance Abuse |
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| Childhood Absence Epilepsy |
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| Alexithymia |
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| Pathological Gambling |
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| Kleptomania |
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| Cutis Laxa, Autosomal Dominant 1 |
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| Major Depressive Disorder |
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| Alcohol Use Disorder |
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| Spinocerebellar Ataxia, Autosomal Recessive 17 |
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| Mood Disorder |
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| Dystonia |
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| Psychotic Disorder |
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| Schizophrenia |
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| Disease Of Mental Health |
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| Tobacco Addiction |
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| Migraine With Or Without Aura 1 |
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| Autosomal Dominant Cerebellar Ataxia |
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| Attention Deficit-Hyperactivity Disorder |
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| Alzheimer Disease, Familial, 1 |
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| Nervous System Disease |
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Orthologs Information
| Species | Symbol | Source | ID |
|---|---|---|---|
| Macaca mulatta | PDYN | VGNC | VGNC:75937 |
| Rattus norvegicus | PDYN | RGD | RGD:62054 |
| Canis familiaris | PDYN | VGNC | VGNC:44398 |
| Felis catus | PDYN | VGNC | VGNC:81145 |
| Bos taurus | PDYN | VGNC | VGNC:32723 |
| Mus musculus | PDYN | MGD | MGI:97535 |
| Others | PDYN | NCBI |