Neurotransmitter disorders (Homo sapiens)

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Aromatic L-Amino Acid Decarboxylase DeficiencyDBH5-Hydroxyindoleacetic acidL-tryptophanEpinephrineSerotoninDopamine3-O-methyldopa5-HydroxytryptophanDopamine Transporter DeficiencyDihydroxyphenylacetic acidTyrosineNormetanephrineNorepinephrineMetanephrineVanillylmandelic acidHomovanillic acidL-DopaMonoamine Oxidase ATyrosine 3-monooxygenase3-methoxy-4-hydroxyphenylglycolDopamine-Serotonin Vesicular Transport Defect3-MethoxytyramineVanillactic acidTyrosine Hydroxylase DeficiencyAromatic L-amino acidMonoamine Oxidase AMonoamine Oxidase ADopamine Beta Hydroxylase DeficiencyMonoamine Oxidase A Deficiency


Description

Neurtotransmitter Disorders

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Quality Tags

Ontology Terms

 

Bibliography

  1. Mark J Crabtree, Keith M Channon; ''Synthesis and recycling of tetrahydrobiopterin in endothelial function and vascular disease''; Nitric Oxide, 2011 PubMed Europe PMC Scholia
  2. Heiko Brennenstuhl, Sabine Jung-Klawitter, Birgit Assmann, Thomas Opladen; ''Inherited Disorders of Neurotransmitters: Classification and Practical Approaches for Diagnosis and Treatment''; Neuropediatrics ., 2019 PubMed Europe PMC Scholia
  3. C A Nichol, C L Lee, M P Edelstein, J Y Chao, D S Duch; ''Biosynthesis of tetrahydrobiopterin by de novo and salvage pathways in adrenal medulla extracts, mammalian cell cultures, and rat brain in vivo''; Proc Natl Acad Sci U S A ., 1983 PubMed Europe PMC Scholia
  4. Nenad Blau, Marinus Duran, K Michael Gibson, Carlo Dionisi-Vici; ''Physician's Guide to the Diagnosis, Treatment, and Follow-Up of Inherited Metabolic Diseases''; Springer-Verlag Berlin Heidelberg, 2014

History

View all...
CompareRevisionActionTimeUserComment
128514view00:56, 11 February 2024EweitzSoften disease color
128299view04:24, 30 January 2024EweitzUse standard shape for pathway nodes
127617view20:11, 8 November 2023LarsgwFix reference bp:DB
126301view12:36, 20 April 2023DeSlConverted another MAOA from Metabolite to Protein type
126300view12:35, 20 April 2023DeSlConverted MAOA from Metabolite to Protein type
124951view08:05, 7 January 2023EgonwUpgraded http->httpS in OMIM links
123757view12:29, 12 August 2022DeSlAdded legend
123756view12:27, 12 August 2022DeSlAdded alias for disorder
123755view12:25, 12 August 2022DeSlOntology Term : 'Parkinsonism' added !
123754view12:25, 12 August 2022DeSlOntology Term : 'dystonia' added !
123753view12:24, 12 August 2022DeSlOntology Term : 'Brunner Syndrome' added !
123752view12:23, 12 August 2022DeSlOntology Term : 'Segawa syndrome pathway' added !
123751view12:22, 12 August 2022DeSlOntology Term : 'tryptophan metabolic pathway' added !
123750view12:22, 12 August 2022DeSlOntology Term : 'tryptophan degradation pathway' added !
123749view12:22, 12 August 2022DeSlOntology Term : 'tyrosine degradation pathway' added !
123748view12:22, 12 August 2022DeSlOntology Term : 'tyrosine metabolic pathway' added !
123747view12:21, 12 August 2022DeSlOntology Term : 'epinephrine degradation pathway' added !
123746view12:21, 12 August 2022DeSlOntology Term : 'epinephrine metabolic pathway' added !
123745view12:21, 12 August 2022DeSlOntology Term : 'epinephrine biosynthetic pathway' added !
123744view12:21, 12 August 2022DeSlOntology Term : 'serotonin metabolic pathway' added !
123743view12:20, 12 August 2022DeSlOntology Term : 'serotonin biosynthetic pathway' added !
123742view12:20, 12 August 2022DeSlOntology Term : 'dopamine biosynthetic pathway' added !
123741view12:20, 12 August 2022DeSlOntology Term : 'dopamine metabolic pathway' added !
123740view12:20, 12 August 2022DeSlOntology Term : 'dopamine degradation pathway' added !
123739view12:19, 12 August 2022DeSlAnnotated missing metabolite 5-HIAL
123738view12:17, 12 August 2022DeSlAdding additional details from norephinephrine to VMA and MOPG conversions
123737view09:19, 12 August 2022DeSlAdded some more details on reactions, including lit. ref.
123736view09:11, 12 August 2022DeSlAdded protein complexes + cofactors to reactions starting from Tyr and Try, including lit. refs.
123735view08:52, 12 August 2022DeSlChecked full PW for Ed. 5, updated links to disorders, added transporter enzymes, added ref for full PW
120526view02:00, 11 December 2021EweitzFix case
119285view10:50, 23 June 2021FinterlyAdded ISBN for book citation
117163view09:48, 18 May 2021EweitzModified title
106196view12:09, 16 August 2019MaintBotHMDB identifier normalization
104416view06:26, 24 May 2019MaintBotRemoved the RHEA: prefix from the identifier.
104392view13:56, 23 May 2019Mkutmonfixed reference
104391view13:52, 23 May 2019Mkutmonadd Rhea identifiers
104029view17:42, 25 April 2019IreneHemelModified description
98921view05:17, 16 October 2018EgonwModified description
98251view09:36, 15 August 2018DeSlFixed layout
98250view09:34, 15 August 2018DeSlChanged layout of disease nodes
97385view03:58, 14 May 2018Khanspersdecreased board height
97384view03:57, 14 May 2018Khanspersdecreased board height
97366view10:07, 11 May 2018DeSlChanged layout, connected 5HTP as side metabolite (like chapter indicates), changed disease nodes to labels (with links).
96271view15:59, 3 March 2018EgonwFixed a datanode misclassification
96217view08:57, 1 March 2018DeSlModified description
96207view09:15, 28 February 2018AnneFriesacherModified description
96188view15:37, 23 February 2018AnneFriesacherAdded comments on diseases, added literature reference
96187view15:23, 23 February 2018AnneFriesacherEdited IDs
96186view15:05, 23 February 2018AnneFriesacher
96185view13:46, 23 February 2018DeSlAdded OMIM IDs for disease

External references

DataNodes

View all...
NameTypeDatabase referenceComment
3-MethoxytyramineMetaboliteCHEBI:1582 (ChEBI)
3-O-methyldopaMetaboliteCHEBI:133668 (ChEBI)
3-methoxy-4-hydroxyphenylglycolMetaboliteQ223097 (Wikidata)
5-Hydroxyindoleacetic acidMetaboliteCHEBI:27823 (ChEBI)
5-HydroxytryptophanMetaboliteCHEBI:17780 (ChEBI)
Aromatic L-Amino Acid Decarboxylase Deficiency
Aromatic L-amino acidMetaboliteCHEBI:33856 (ChEBI)
DBHGeneProductENSG00000123454 (Ensembl)
Dihydroxyphenylacetic acidMetaboliteCHEBI:41941 (ChEBI)
Dopamine Beta Hydroxylase Deficiency
Dopamine Transporter Deficiency
Dopamine-Serotonin Vesicular Transport Defect
DopamineMetaboliteCHEBI:1764 (ChEBI)
EpinephrineMetaboliteQ132621 (Wikidata)
Homovanillic acidMetaboliteCHEBI:5758 (ChEBI)
L-DopaMetaboliteCHEBI:1377 (ChEBI)
L-tryptophanMetaboliteCHEBI:21407 (ChEBI)
MetanephrineMetaboliteHMDB04063 (HMDB)
Monoamine Oxidase A Deficiency
Monoamine Oxidase AMetabolite4128 (Entrez Gene)
NorepinephrineMetaboliteCHEBI:1 (ChEBI)
NormetanephrineMetaboliteQ517109 (Wikidata)
SerotoninMetaboliteCHEBI:1420 (ChEBI)
Tyrosine 3-monooxygenaseProteinE7EQI0 (Uniprot-TrEMBL)
Tyrosine Hydroxylase Deficiency
TyrosineMetaboliteCHEBI:15277 (ChEBI)
Vanillactic acidMetaboliteHMDB00913 (HMDB)
Vanillylmandelic acidMetaboliteCHEBI:1573 (ChEBI)

Annotated Interactions

No annotated interactions

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