Difference between revisions of "FlyBase:Human Disease Model Report"

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Last Updated:  
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Last Updated: 15 Dec. 2017
  
Introduction
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This is a field-by-field guide to the information provided in the '''Human Disease Model Report'''.
  
 
==General Information==
 
==General Information==
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|'''FlyBase ID'''||  The Primary FlyBase identifier number of the human disease, used to uniquely identify the Human Disease Model in the database.  
 
|'''FlyBase ID'''||  The Primary FlyBase identifier number of the human disease, used to uniquely identify the Human Disease Model in the database.  
 
|-
 
|-
|'''Disease Ontology ID'''|| Links to [http://disease-ontology.org/ Disease Ontology] term report in the [http://flybase.org/static_pages/termlink/termlink.html/ Vocabularies] tool.
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|'''Disease Ontology ID'''|| Links to [http://disease-ontology.org/ Disease Ontology] term report in the [http://{{flybaseorg}}/static_pages/termlink/termlink.html Vocabularies] tool.
 
|-
 
|-
 
|'''Parent Disease '''|| Links to parent entity, which describes general and shared information for the phenotypic series. Specific (child) diseases are usually defined by a single causative human gene.
 
|'''Parent Disease '''|| Links to parent entity, which describes general and shared information for the phenotypic series. Specific (child) diseases are usually defined by a single causative human gene.
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|'''OMIM'''|| Links to relevant [http://omim.org/ OMIM] phenotype report.
 
|'''OMIM'''|| Links to relevant [http://omim.org/ OMIM] phenotype report.
 
|-
 
|-
|'''Parent Disease DOID '''|| Links to [http://disease-ontology.org/ Disease Ontology] term report for the Parent Disease in the [http://flybase.org/static_pages/termlink/termlink.html/ Vocabularies] tool.
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|'''Parent Disease DOID '''|| Links to [http://disease-ontology.org/ Disease Ontology] term report for the Parent Disease in the [http://{{flybaseorg}}/static_pages/termlink/termlink.html Vocabularies] tool.
 
|}
 
|}
  
 
==Overview==
 
==Overview==
  
The overview is a brief summary of the ''Drosophila'' human disease model, and offers a  It includes the FlyBase disease name, the human gene implicated, the ''Drosophila'' ortholog(s) of the implicated human gene, the nature of available genetic reagents, whether the human gene has been transgenically expressed, the nature of transgenically expressed human constructs, whether the human gene has been used to heterologously rescue ''Drosophila'' loss-of-function phenotypes, the kinds of experiments that have been performed, and whether therapeutic agents have been screened.
+
The Overview is a brief summary of the ''Drosophila'' human disease model. For specific disease models, it includes (1) the FlyBase disease name, any abbreviation commonly used, and the pattern of inheritance in human (e.g., autosomal dominant); (2) the human gene implicated, with a brief mention of known or postulated function and whether it is implicated in any additional diseases; (3) the Drosophila ortholog(s) of the implicated human gene, the nature of available genetic reagents for that gene, and whether other human genes are orthologous to that fly gene; (4) whether the human gene has been transgenically introduced into flies, the nature of transgenically expressed constructs, whether the human gene has been used to heterologously rescue Drosophila loss-of-function phenotypes; (5) variants implicated in human disease that have been characterized, whether in the context of a transgenic human gene or an analagous mutation in the fly gene; (6) highlights of phenotype(s) of the fly gene and whether genetic and/or physical interaction data are available. Records that do not conform to this pattern include reports for phenotypic series and for induced models (diet- or chemically-induced, for example). The Overview is date-stamped to reflect the last curator update.
  
 
==Disease Summary Information==
 
==Disease Summary Information==
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{| class="wikitable" style="width: 100%;"
 
{| class="wikitable" style="width: 100%;"
|'''OMIM report '''|| style="width: 80%;" | field text
+
|'''Symptoms and phenotype '''|| style="width: 80%;" | Describes symptoms and phenotypes shared by diseases in the relevant phenotypic series. Entry includes links to outside source, and is date-stamped as to when a FlyBase curator last consulted the source.
 +
|}
 +
 
 +
===Specific Disease Summary===
 +
 
 +
 
 +
{| class="wikitable" style="width: 100%;"
 +
|'''OMIM report '''|| style="width: 80%;" | Links to relevant [http://omim.org/ OMIM] phenotype report.
 
|-
 
|-
|'''Symptoms and phenotype '''|| field text
+
|'''Symptoms and phenotype '''|| Describes symptoms and phenotypes characteristic of the disease. Entry includes links to outside source, and is date-stamped as to when a FlyBase curator last consulted the source.
 
|-
 
|-
|'''Genetics '''|| field text
+
|'''Genetics '''|| Describes the genetics of the disease, including causative human gene, and pattern of inheritance. Entry includes links to outside source, and is date-stamped as to when a FlyBase curator last consulted the source.
 
|-
 
|-
|'''Cellular phenotype and pathology '''|| field text
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|'''Cellular phenotype and pathology '''|| Describes the cellular phenotype and pathology characteristic of the disease.  Entry includes links to outside source, and is date-stamped as to when a FlyBase curator last consulted the source.
 
|-
 
|-
|'''Molecular information '''|| field text
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|'''Molecular information '''|| Describes molecular information relevant to the disease, including information about the function of the causative gene, molecular information about mutations in the causative gene, and/or molecular information about mutant isoforms of the causative protein. Entry includes links to outside source, and is date-stamped as to when a FlyBase curator last consulted the source.
 
|-
 
|-
|'''External links '''|| field text
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|'''External links '''|| A list of links to external databases and resources providing additional background concerning the disease. These include:
 +
 
 +
[http://www.genecards.org/ Gene Cards]
 +
 
 +
[http://www.ncbi.nlm.nih.gov/books/ GeneReviews, NCBI Bookshelf]
 +
 
 +
[http://ghr.nlm.nih.gov/condition/ Genetics Home Reference (condition)]
 +
 
 +
[http://ghr.nlm.nih.gov/gene/ Genetics Home Reference (gene)]
 +
 
 +
[http://ghr.nlm.nih.gov/geneFamily/ Genetics Home Reference (geneFamily)]
 +
 
 +
[http://www.kegg.jp/kegg/pathway.html KEGG Disease Pathways]
 +
 
 +
[https://www.ncbi.nlm.nih.gov/medgen/ NCBI MedGen]
 +
 
 +
[https://www.ncbi.nlm.nih.gov/gene/ NCBI (Entrez) gene]
 +
 
 +
[http://www.gene2function.org/search/ Gene2Function (human gene)]
 +
 
 +
[http://marrvel.org MARRVEL (gene)]
 +
 
 +
[http://www.informatics.jax.org/disease/ MGI Human-Mouse Disease Connection]
 
|-
 
|-
|'''Disease synonyms '''|| field text
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|'''Disease synonyms '''|| A listing of other names, abbreviations, acronyms and terms that have been used to refer to the disease.
 
|}
 
|}
  
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{| class="wikitable" style="width: 100%;"
 
{| class="wikitable" style="width: 100%;"
|'''Related human health report(s) '''|| style="width: 80%;" | field text
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|'''Related human health report(s) '''|| style="width: 80%;" | Links to the Report(s) of disease(s) that are related to the disease that is the subject of a Human Disease Model Report, but is not a member of the same phenotypic series. For example, the diseases could be related by having the same causative human gene.
 
|}
 
|}
  
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{| class="wikitable" style="width: 100%;"
 
{| class="wikitable" style="width: 100%;"
|'''OMIM phenotypic series '''|| style="width: 80%;" | field text
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|'''OMIM phenotypic series '''|| style="width: 80%;" | Links to relevant [https://omim.org/phenotypicSeriesTitle/all OMIM phenotypic series]. An OMIM phenotypic series is a tabular view of genetic heterogeneity of similar phenotypes across the genome.
 
|}
 
|}
  
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{| class="wikitable" style="width: 100%;"
 
{| class="wikitable" style="width: 100%;"
|'''Human gene (HGNC) '''|| style="width: 80%;" | field text
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|'''Human gene (HGNC) '''|| style="width: 80%;" | Links to HUGO Gene Nomenclature Committee ([http://www.genenames.org/ HGNC]) symbol report.
 
|-
 
|-
|'''Human gene (FlyBase) '''|| field text
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|'''Human gene (FlyBase) '''|| Links to FlyBase [http://{{flybaseorg}}/wiki/FlyBase:Gene_Report Gene Report] of human gene transgenically expressed in flies.
 
|-
 
|-
|'''D. melanogaster ortholog (based on DIOPT) '''|| field text
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|'''D. melanogaster ortholog (based on DIOPT) '''|| Links to FlyBase [http://{{flybaseorg}}/wiki/FlyBase:Gene_Report Gene Report] of ''Drosophila'' gene orthologous to HGNC gene. Orthology determined by [http://www.flyrnai.org/cgi-bin/DRSC_orthologs.pl/ DIOPT] analysis resulting from the combined predictions of multiple ortholog prediction algorithms.
 
|-
 
|-
|'''Comments on ortholog(s) '''|| field text
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|'''Comments on ortholog(s) '''|| Comments on the nature of the orthology of the human to ''Drosophila'' gene(s), e.g., one to one, one to many, many to one, many to many, as defined by [http://orthodb.org/ OrthoDB] ortholog prediction.
 
|-
 
|-
|'''Other mammalian ortholog(s) used '''|| field text
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|'''Other mammalian ortholog(s) used '''|| Links to FlyBase [http://{{flybaseorg}}/wiki/FlyBase:Gene_Report Gene Report] of nonhuman mammalian gene transgenically expressed in flies.
 
|}
 
|}
  
 
==D. melanogaster Gene Information==
 
==D. melanogaster Gene Information==
 +
Drosophila gene(s) identified as model(s) of this disease.
  
field text
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{| class="wikitable" style="width: 100%;"
 +
|'''Molecular function (GO)'''|| style="width: 80%;" | A summary of the [http://geneontology.org/ Gene Ontology] [http://geneontology.org/page/molecular-function-ontology-guidelines molecular function] terms associated with the ''Drosophila'' gene orthologous to the causative human gene.
 +
|-
 +
|'''Cellular component (GO)'''|| A summary of the [http://geneontology.org/ Gene Ontology] [http://geneontology.org/page/cellular-component-ontology-guidelines cellular component] terms associated with the ''Drosophila'' gene orthologous to the causative human gene.
 +
|-
 +
|'''Comments on ortholog(s) '''|| Comments on the nature of the orthology of the ''Drosophila'' to human gene(s), e.g., one to one, one to many, many to one, many to many, as defined by [http://orthodb.org/ OrthoDB] ortholog prediction. Comment concerning protein identity and similarity between Drosophila protein and the human ortholog; alignment determined by [http://www.flyrnai.org/cgi-bin/DRSC_orthologs.pl/ DIOPT] analysis
 +
|-
 +
|'''Orthologs and Alignments from DRSC '''|| Links to [http://www.flyrnai.org/cgi-bin/DRSC_orthologs.pl/ DIOPT] tool; the H.sapiens (Human) link pre-fills the DIOPT interface with the ''Drosophila'' gene to search for its human ortholog.
 +
|}
  
 
==Synthetic Gene(s) Used==
 
==Synthetic Gene(s) Used==
  
field text
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Links to FlyBase [http://{{flybaseorg}}/wiki/FlyBase:Gene_Report Gene Report] of artificial gene transgenically expressed in flies (e.g. a CAG repeat construct or hexanucleotide repeat construct). Such genes have the feature type engineered_foreign_region.
  
 
==Experimental Findings==
 
==Experimental Findings==
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===Summary===
 
===Summary===
  
field text
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This section used only for original test-case disease model reports; for most human disease model reports this section is blank.
 
 
===Human Disease Wiki (Experimental Findings)===
 
 
 
{| class="wikitable" style="width: 100%;"
 
|'''User Contributed Commentary '''|| style="width: 80%;" | field text
 
|}
 
  
 
===Description of Experiments===
 
===Description of Experiments===
  
 
{| class="wikitable" style="width: 100%;"
 
{| class="wikitable" style="width: 100%;"
|'''Mammalian transgenics: heterologous rescue '''|| style="width: 80%;" | field text
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|'''Mammalian transgenics: heterologous rescue ''' || style="width: 80%;" | Free text description of use of human or other mammalian transgene to rescue loss-of-function phenotypes of a mutation in its orthologous ''Drosophila'' gene. A listing of genetic reagents used in experiments, linked to relevant [http://{{flybaseorg}}/wiki/FlyBase:Allele_Report Allele Reports], are appended to the end of the statement. Every statement is linked to a supporting [http://{{flybaseorg}}/wiki/FlyBase:Reference_Report Reference Report].
 +
|-
 +
|'''Mammalian transgenics: transgenic phenotype '''|| Free text description of phenotypes resulting from tissue-specific transgenic expression of human or other mammalian disease-associated protein, with a focus on disease model relevance. A listing of genetic reagents used in experiments, linked to relevant [http://{{flybaseorg}}/wiki/FlyBase:Allele_Report Allele Reports], are appended to the end of the statement. Every statement is linked to a supporting [http://{{flybaseorg}}/wiki/FlyBase:Reference_Report Reference Report].
 
|-
 
|-
|'''Mammalian transgenics: transgenic phenotype '''|| field text
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|'''Mammalian transgenics: interactions '''|| Free text description of genetic and/or physical interactions observed between transgenically expressed human or other mammalian protein and Drosophila genes/proteins and/or other transgenically expressed human or mammalian genes/proteins, with a focus on disease model relevance. A listing of genetic reagents used in experiments, linked to relevant [http://{{flybaseorg}}/wiki/FlyBase:Allele_Report Allele Reports], are appended to the end of the statement. Every statement is linked to a supporting [http://{{flybaseorg}}/wiki/FlyBase:Reference_Report Reference Report].
 
|-
 
|-
|'''Mammalian transgenics: interactions '''|| field text
 
 
|-
 
|-
|'''Mammalian transgenics: pertubations and treatments '''|| field text
+
|'''Mammalian transgenics: pertubations and treatments '''|| Free text description of the effect of chemical or environmental perturbations or treatments on the phenotypes resulting from transgenically expressed human or other mammalian protein, with a focus on disease model relevance. This field is also used to describe drug discovery and/or drug screening experiments. A listing of genetic reagents used in experiments, linked to relevant [http://{{flybaseorg}}/wiki/FlyBase:Allele_Report Allele Reports], are appended to the end of the statement. Every statement is linked to a supporting [http://{{flybaseorg}}/wiki/FlyBase:Reference_Report Reference Report].
 
|-
 
|-
|'''Drosophila genes: relevant phenotypes '''|| field text
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|'''Drosophila genes: relevant phenotypes '''|| Free text description of phenotypes resulting from mutations in or RNAi knockdown of the ''Drosophila'' ortholog of a human disease-associated gene, with a focus on disease model relevance. A listing of genetic reagents used in experiments, linked to relevant [http://{{flybaseorg}}/wiki/FlyBase:Allele_Report Allele Reports], are appended to the end of the statement. Every statement is linked to a supporting [http://{{flybaseorg}}/wiki/FlyBase:Reference_Report Reference Report].
 
|-
 
|-
|'''Drosophila genes: interactions '''|| field text
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|'''Drosophila genes: interactions '''|| Free text description of genetic and/or physical interactions observed between the ''Drosophila'' ortholog of a human disease-associated gene and Drosophila genes/proteins and/or other transgenically expressed human or mammalian genes/proteins, with a focus on disease model relevance .A listing of genetic reagents used in experiments, linked to relevant [http://{{flybaseorg}}/wiki/FlyBase:Allele_Report Allele Reports], are appended to the end of the statement. Every statement is linked to a supporting [http://{{flybaseorg}}/wiki/FlyBase:Reference_Report Reference Report].
 
|-
 
|-
|'''Drosophila genes: pertubations and treatments '''|| field text
+
|'''Drosophila genes: pertubations and treatments '''|| Free text description of the effect of chemical or environmental perturbations or treatments on the phenotypes resulting from mutations in, RNAi knockdown of, or transgenic overexpression of the ''Drosophila'' ortholog of a human disease-associated gene,, with a focus on disease model relevance. This field is also used to describe drug discovery and/or drug screening experiments. A listing of genetic reagents used in experiments, linked to relevant [http://{{flybaseorg}}/wiki/FlyBase:Allele_Report Allele Reports], are appended to the end of the statement. Every statement is linked to a supporting [http://{{flybaseorg}}/wiki/FlyBase:Reference_Report Reference Report].
 
|-
 
|-
|'''Drosophila recombinant constructs: phenotype or rescue '''|| field text
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|'''Drosophila recombinant constructs: phenotype or rescue '''|| Free text description of phenotypes resulting from transgenic overexpression of the ''Drosophila'' ortholog of a human disease-associated gene, or of the use of ''Drosophila'' transgene to rescue loss-of-function phenotypes of a mutation in the ''Drosophila'' ortholog of a human disease-associated gene. A listing of genetic reagents used in experiments, linked to relevant [http://{{flybaseorg}}/wiki/FlyBase:Allele_Report Allele Reports], are appended to the end of the statement. Every statement is linked to a supporting [http://{{flybaseorg}}/wiki/FlyBase:Reference_Report Reference Report].
 
|-
 
|-
|'''Additional information '''|| field text
+
|'''Additional information '''|| Free text descriptions of experiments that are not covered in other descriptive fields, including but not exclusive to gene expression patterns, experiments conducted in cell culture, details of protein structural domains or gene models, and experiments or observations in other organisms. Every statement is linked to a supporting [http://{{flybaseorg}}/wiki/FlyBase:Reference_Report Reference Report].
 
|-
 
|-
|'''Proposed mechanisms '''|| field text
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|'''Proposed mechanisms '''|| Free text description of key findings concerning disease mechanism that have been discovered or confirmed in ''Drosophila'' experiments. Every statement is linked to a supporting [http://{{flybaseorg}}/wiki/FlyBase:Reference_Report Reference Report].
 
|}
 
|}
  
 
==Summary of Physical Interactions==
 
==Summary of Physical Interactions==
  
field text
+
Information regarding curated physical interactions for the protein and RNA products of the gene. Currently, only interactions involving two D. melanogaster genes are reported. Only pair-wise interactions are reported. Information is imported from existing [http://{{flybaseorg}}/wiki/FlyBase:Interaction_Report Interaction Reports].
  
 
==Alleles Reported to Model Human Disease (Disease Ontology)==
 
==Alleles Reported to Model Human Disease (Disease Ontology)==
  
field text
+
 
 +
Human Disease model data curated using disease terms from the [http://disease-ontology.org/ Disease Ontology].
 +
 
 +
{| class="wikitable" style="width: 100%;"
 +
|-
 +
|'''Models''' || style="width: 80%;" | A table showing any human disease(s) that are being modelled by a given mutant or transgenic allele.  The phenotype(s) being studied must recapitulate some aspect of the human disease for the allele to be considered a model. In some cases, an allele may be expected to produce a disease phenotype but does not. These unexpectedly negative results are also shown.
 +
 
 +
The table consists of four columns
 +
 
 +
'''Allele''' - The alleles of the gene that is being used as a model.
 +
 
 +
'''Disease''' - Indicates whether or not the allele is modeling the disease ('model of' or ''''DOES NOT''' model') followed by the name of the disease (from the [http://disease-ontology.org/ Disease Ontology]).
 +
 
 +
'''Evidence''' - If the allele models the phenotype on its own 'Inferred from mutant phenotype' is displayed. If the mutant phenotype is only observed in combination with another allele 'In combination with' is displayed followed by the symbols of other allele(s), with hyperlinks to the relevant allele report pages. Note that any drivers that are required for the expression of transgenic alleles are not listed in this section.
 +
 
 +
'''References''' - lists the reference(s) that describe the model.
 +
 
 +
This information is also shown on the individual [http://{{flybaseorg}}/wiki/FlyBase:Allele_Report Allele Reports].
 +
|-
 +
|'''Interactions''' || A table showing interactions of this allele with other disease-causing allele(s)
 +
 
 +
The table consists of four columns
 +
 
 +
'''Allele''' - The alleles of the gene that is being used as a model.
 +
 
 +
'''Disease''' - the nature of the interaction ('exacerbates' or 'ameliorates' and the name of the disease (from the [http://disease-ontology.org/ Disease Ontology]). This column also indicates if the allele is not modifying a disease (prefixed with '''DOES NOT''').
 +
 
 +
'''Interaction''' - 'modeled by' followed by the symbol of the allele that is modeling the disease, with hyperlinks to the relevant allele report pages.
 +
 
 +
'''References''' - lists the reference(s) that describes the model.
 +
 
 +
This information is also shown on the individual [http://{{flybaseorg}}/wiki/FlyBase:Allele_Report Allele Reports].
 +
|}
  
 
==Genetic Tools, Stocks and Reagents==
 
==Genetic Tools, Stocks and Reagents==
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{| class="wikitable" style="width: 100%;"
 
{| class="wikitable" style="width: 100%;"
|'''Bloomington Stock Center Disease Page'''|| style="width: 80%;" | field text
+
|'''Bloomington Stock Center Disease Page'''|| style="width: 80%;" | Links to relevant [https://bdsc.indiana.edu/stocks/hd/index.html BDSC Human Disease Model page].
 
|}
 
|}
  
 
===Selected mammalian transgenes===
 
===Selected mammalian transgenes===
  
A table that consists of three columns:
+
For human or mammalian transgene(s) used to model this disease, transgenic constructs presented as a table that consists of three columns (below). If there are ten or fewer constructs, all are listed. For larger numbers, a selected sample weighted for availability of stocks, frequency of citations, and more recent citations.
  
'''Allele''' - field text
+
'''Allele''' - Links to the [http://{{flybaseorg}}/wiki/FlyBase:Allele_Report Allele Report] for the human or other mammalian transgene.
  
'''Transgene''' - field text
+
'''Transgene''' - Links to the [http://{{flybaseorg}}/wiki/FlyBase:Recombinant_Construct_Report Recombinant Construct Report] for the human or other mammalian transgene.
  
'''Publicly Available Stocks''' - field text
+
'''Publicly Available Stocks''' - Links to the [http://{{flybaseorg}}/wiki/FlyBase:Stock_Report Stock Report] for those human or mammalian transgenes available from a public stock center.
  
 
===Selected Drosophila transgenes===
 
===Selected Drosophila transgenes===
  
A table that consists of three columns:
+
For Drosophila gene(s) used to model this disease, transgenic constructs and associated alleles presented as a table that consists of three columns (below). All alleles of transgenic constructs associated with a disease ontology term are listed. Additional listings weighted for availability of stocks, frequency of citations, and more recent citations.
  
'''Allele''' - field text
+
'''Allele''' - Links to the [http://{{flybaseorg}}/wiki/FlyBase:Allele_Report Allele Report] for the ''Drosophila'' transgene.
  
'''Transgene''' - field text
+
'''Transgene''' - Links to the [http://{{flybaseorg}}/wiki/FlyBase:Recombinant_Construct_Report Recombinant Construct Report] for the ''Drosophila'' transgene.
  
'''Publicly Available Stocks''' - field text
+
'''Publicly Available Stocks''' - Links to the [http://{{flybaseorg}}/wiki/FlyBase:Stock_Report Stock Report] for those ''Drosophila'' transgenes available from a public stock center.
  
 
===RNAi constructs available===
 
===RNAi constructs available===
  
A table that consists of three columns:
+
For Drosophila gene(s) used to model this disease, all RNAi constructs; presented as a table that consists of three columns:
  
'''Allele''' - field text
+
'''Allele''' - Links to the [http://{{flybaseorg}}/wiki/FlyBase:Allele_Report Allele Report] for the RNAi construct.
  
'''Transgene''' - field text
+
'''Transgene''' - Links to the [http://{{flybaseorg}}/wiki/FlyBase:Recombinant_Construct_Report Recombinant Construct Report] for the RNAi construct.
  
'''Publicly Available Stocks''' - field text
+
'''Publicly Available Stocks''' - Links to the [http://{{flybaseorg}}/wiki/FlyBase:Stock_Report Stock Report] for those RNAi constructs available from a public stock center.
  
 
===Selected Drosophila classical alleles===
 
===Selected Drosophila classical alleles===
  
A table that consists of four columns:
+
For Drosophila gene(s) used to model this disease, alleles presented as a table that consists of four columns (below). All classical alleles associated with a disease ontology term and/or described as amorphic are listed; if no amorphic alleles have been reported, loss-of-function alleles are listed.
 
   
 
   
'''Allele''' - field text
+
'''Allele''' - Links to the [http://{{flybaseorg}}/wiki/FlyBase:Allele_Report Allele Report] for the ''Drosophila'' classical mutant.
  
'''Allele class''' - field text
+
'''Allele class''' - Lists the [http://{{flybaseorg}}/wiki/FlyBase:Controlled_vocabularies_used_by_FlyBase FlyBase CV term] for the allele class to which the allele belongs.
  
'''Mutagen''' - field text
+
'''Mutagen''' - Lists the [http://{{flybaseorg}}/wiki/FlyBase:Controlled_vocabularies_used_by_FlyBase FlyBase CV term] for the mutagen responsible for the genetic lesion causing the mutation.
  
'''Publicly Available Stocks''' - field text
+
'''Publicly Available Stocks''' - Links to the [http://{{flybaseorg}}/wiki/FlyBase:Stock_Report Stock Report] for those ''Drosophila'' classical mutants available from a public stock center.
  
 
===References===
 
===References===
  
field text
+
A list of publications that discuss the human disease model, subdivided into fields by type of publication.

Latest revision as of 20:48, 2 January 2018

Last Updated: 15 Dec. 2017

This is a field-by-field guide to the information provided in the Human Disease Model Report.

General Information

Name The valid full name that is used in FlyBase for the Human Disease Model.
FlyBase ID The Primary FlyBase identifier number of the human disease, used to uniquely identify the Human Disease Model in the database.
Disease Ontology ID Links to Disease Ontology term report in the Vocabularies tool.
Parent Disease Links to parent entity, which describes general and shared information for the phenotypic series. Specific (child) diseases are usually defined by a single causative human gene.
OMIM Links to relevant OMIM phenotype report.
Parent Disease DOID Links to Disease Ontology term report for the Parent Disease in the Vocabularies tool.

Overview

The Overview is a brief summary of the Drosophila human disease model. For specific disease models, it includes (1) the FlyBase disease name, any abbreviation commonly used, and the pattern of inheritance in human (e.g., autosomal dominant); (2) the human gene implicated, with a brief mention of known or postulated function and whether it is implicated in any additional diseases; (3) the Drosophila ortholog(s) of the implicated human gene, the nature of available genetic reagents for that gene, and whether other human genes are orthologous to that fly gene; (4) whether the human gene has been transgenically introduced into flies, the nature of transgenically expressed constructs, whether the human gene has been used to heterologously rescue Drosophila loss-of-function phenotypes; (5) variants implicated in human disease that have been characterized, whether in the context of a transgenic human gene or an analagous mutation in the fly gene; (6) highlights of phenotype(s) of the fly gene and whether genetic and/or physical interaction data are available. Records that do not conform to this pattern include reports for phenotypic series and for induced models (diet- or chemically-induced, for example). The Overview is date-stamped to reflect the last curator update.

Disease Summary Information

Parent Disease Summary

Symptoms and phenotype Describes symptoms and phenotypes shared by diseases in the relevant phenotypic series. Entry includes links to outside source, and is date-stamped as to when a FlyBase curator last consulted the source.

Specific Disease Summary

OMIM report Links to relevant OMIM phenotype report.
Symptoms and phenotype Describes symptoms and phenotypes characteristic of the disease. Entry includes links to outside source, and is date-stamped as to when a FlyBase curator last consulted the source.
Genetics Describes the genetics of the disease, including causative human gene, and pattern of inheritance. Entry includes links to outside source, and is date-stamped as to when a FlyBase curator last consulted the source.
Cellular phenotype and pathology Describes the cellular phenotype and pathology characteristic of the disease. Entry includes links to outside source, and is date-stamped as to when a FlyBase curator last consulted the source.
Molecular information Describes molecular information relevant to the disease, including information about the function of the causative gene, molecular information about mutations in the causative gene, and/or molecular information about mutant isoforms of the causative protein. Entry includes links to outside source, and is date-stamped as to when a FlyBase curator last consulted the source.
External links A list of links to external databases and resources providing additional background concerning the disease. These include:

Gene Cards

GeneReviews, NCBI Bookshelf

Genetics Home Reference (condition)

Genetics Home Reference (gene)

Genetics Home Reference (geneFamily)

KEGG Disease Pathways

NCBI MedGen

NCBI (Entrez) gene

Gene2Function (human gene)

MARRVEL (gene)

MGI Human-Mouse Disease Connection

Disease synonyms A listing of other names, abbreviations, acronyms and terms that have been used to refer to the disease.

Related Diseases

Related human health report(s) Links to the Report(s) of disease(s) that are related to the disease that is the subject of a Human Disease Model Report, but is not a member of the same phenotypic series. For example, the diseases could be related by having the same causative human gene.

Related Specific Diseases

OMIM phenotypic series Links to relevant OMIM phenotypic series. An OMIM phenotypic series is a tabular view of genetic heterogeneity of similar phenotypes across the genome.

A table that consists of four columns:

Disease - Consists of OMIM symbol, links to OMIM phenotype report.

Associated Human gene(s) - Consists of OMIM symbol, links to OMIM genotype report.

Drosophila model - Consists of valid full name that is used in FlyBase for the disease, links to Human Disease Model Report.

Human transgene in Drosophila - "y" or no entry; has the human ortholog been transgenically expressed in flies.

Ortholog Information

Human gene (HGNC) Links to HUGO Gene Nomenclature Committee (HGNC) symbol report.
Human gene (FlyBase) Links to FlyBase Gene Report of human gene transgenically expressed in flies.
D. melanogaster ortholog (based on DIOPT) Links to FlyBase Gene Report of Drosophila gene orthologous to HGNC gene. Orthology determined by DIOPT analysis resulting from the combined predictions of multiple ortholog prediction algorithms.
Comments on ortholog(s) Comments on the nature of the orthology of the human to Drosophila gene(s), e.g., one to one, one to many, many to one, many to many, as defined by OrthoDB ortholog prediction.
Other mammalian ortholog(s) used Links to FlyBase Gene Report of nonhuman mammalian gene transgenically expressed in flies.

D. melanogaster Gene Information

Drosophila gene(s) identified as model(s) of this disease.

Molecular function (GO) A summary of the Gene Ontology molecular function terms associated with the Drosophila gene orthologous to the causative human gene.
Cellular component (GO) A summary of the Gene Ontology cellular component terms associated with the Drosophila gene orthologous to the causative human gene.
Comments on ortholog(s) Comments on the nature of the orthology of the Drosophila to human gene(s), e.g., one to one, one to many, many to one, many to many, as defined by OrthoDB ortholog prediction. Comment concerning protein identity and similarity between Drosophila protein and the human ortholog; alignment determined by DIOPT analysis
Orthologs and Alignments from DRSC Links to DIOPT tool; the H.sapiens (Human) link pre-fills the DIOPT interface with the Drosophila gene to search for its human ortholog.

Synthetic Gene(s) Used

Links to FlyBase Gene Report of artificial gene transgenically expressed in flies (e.g. a CAG repeat construct or hexanucleotide repeat construct). Such genes have the feature type engineered_foreign_region.

Experimental Findings

Summary

This section used only for original test-case disease model reports; for most human disease model reports this section is blank.

Description of Experiments

Mammalian transgenics: heterologous rescue Free text description of use of human or other mammalian transgene to rescue loss-of-function phenotypes of a mutation in its orthologous Drosophila gene. A listing of genetic reagents used in experiments, linked to relevant Allele Reports, are appended to the end of the statement. Every statement is linked to a supporting Reference Report.
Mammalian transgenics: transgenic phenotype Free text description of phenotypes resulting from tissue-specific transgenic expression of human or other mammalian disease-associated protein, with a focus on disease model relevance. A listing of genetic reagents used in experiments, linked to relevant Allele Reports, are appended to the end of the statement. Every statement is linked to a supporting Reference Report.
Mammalian transgenics: interactions Free text description of genetic and/or physical interactions observed between transgenically expressed human or other mammalian protein and Drosophila genes/proteins and/or other transgenically expressed human or mammalian genes/proteins, with a focus on disease model relevance. A listing of genetic reagents used in experiments, linked to relevant Allele Reports, are appended to the end of the statement. Every statement is linked to a supporting Reference Report.
Mammalian transgenics: pertubations and treatments Free text description of the effect of chemical or environmental perturbations or treatments on the phenotypes resulting from transgenically expressed human or other mammalian protein, with a focus on disease model relevance. This field is also used to describe drug discovery and/or drug screening experiments. A listing of genetic reagents used in experiments, linked to relevant Allele Reports, are appended to the end of the statement. Every statement is linked to a supporting Reference Report.
Drosophila genes: relevant phenotypes Free text description of phenotypes resulting from mutations in or RNAi knockdown of the Drosophila ortholog of a human disease-associated gene, with a focus on disease model relevance. A listing of genetic reagents used in experiments, linked to relevant Allele Reports, are appended to the end of the statement. Every statement is linked to a supporting Reference Report.
Drosophila genes: interactions Free text description of genetic and/or physical interactions observed between the Drosophila ortholog of a human disease-associated gene and Drosophila genes/proteins and/or other transgenically expressed human or mammalian genes/proteins, with a focus on disease model relevance .A listing of genetic reagents used in experiments, linked to relevant Allele Reports, are appended to the end of the statement. Every statement is linked to a supporting Reference Report.
Drosophila genes: pertubations and treatments Free text description of the effect of chemical or environmental perturbations or treatments on the phenotypes resulting from mutations in, RNAi knockdown of, or transgenic overexpression of the Drosophila ortholog of a human disease-associated gene,, with a focus on disease model relevance. This field is also used to describe drug discovery and/or drug screening experiments. A listing of genetic reagents used in experiments, linked to relevant Allele Reports, are appended to the end of the statement. Every statement is linked to a supporting Reference Report.
Drosophila recombinant constructs: phenotype or rescue Free text description of phenotypes resulting from transgenic overexpression of the Drosophila ortholog of a human disease-associated gene, or of the use of Drosophila transgene to rescue loss-of-function phenotypes of a mutation in the Drosophila ortholog of a human disease-associated gene. A listing of genetic reagents used in experiments, linked to relevant Allele Reports, are appended to the end of the statement. Every statement is linked to a supporting Reference Report.
Additional information Free text descriptions of experiments that are not covered in other descriptive fields, including but not exclusive to gene expression patterns, experiments conducted in cell culture, details of protein structural domains or gene models, and experiments or observations in other organisms. Every statement is linked to a supporting Reference Report.
Proposed mechanisms Free text description of key findings concerning disease mechanism that have been discovered or confirmed in Drosophila experiments. Every statement is linked to a supporting Reference Report.

Summary of Physical Interactions

Information regarding curated physical interactions for the protein and RNA products of the gene. Currently, only interactions involving two D. melanogaster genes are reported. Only pair-wise interactions are reported. Information is imported from existing Interaction Reports.

Alleles Reported to Model Human Disease (Disease Ontology)

Human Disease model data curated using disease terms from the Disease Ontology.

Models A table showing any human disease(s) that are being modelled by a given mutant or transgenic allele. The phenotype(s) being studied must recapitulate some aspect of the human disease for the allele to be considered a model. In some cases, an allele may be expected to produce a disease phenotype but does not. These unexpectedly negative results are also shown.

The table consists of four columns

Allele - The alleles of the gene that is being used as a model.

Disease - Indicates whether or not the allele is modeling the disease ('model of' or 'DOES NOT model') followed by the name of the disease (from the Disease Ontology).

Evidence - If the allele models the phenotype on its own 'Inferred from mutant phenotype' is displayed. If the mutant phenotype is only observed in combination with another allele 'In combination with' is displayed followed by the symbols of other allele(s), with hyperlinks to the relevant allele report pages. Note that any drivers that are required for the expression of transgenic alleles are not listed in this section.

References - lists the reference(s) that describe the model.

This information is also shown on the individual Allele Reports.

Interactions A table showing interactions of this allele with other disease-causing allele(s)

The table consists of four columns

Allele - The alleles of the gene that is being used as a model.

Disease - the nature of the interaction ('exacerbates' or 'ameliorates' and the name of the disease (from the Disease Ontology). This column also indicates if the allele is not modifying a disease (prefixed with DOES NOT).

Interaction - 'modeled by' followed by the symbol of the allele that is modeling the disease, with hyperlinks to the relevant allele report pages.

References - lists the reference(s) that describes the model.

This information is also shown on the individual Allele Reports.

Genetic Tools, Stocks and Reagents

Sources of Stocks

Bloomington Stock Center Disease Page Links to relevant BDSC Human Disease Model page.

Selected mammalian transgenes

For human or mammalian transgene(s) used to model this disease, transgenic constructs presented as a table that consists of three columns (below). If there are ten or fewer constructs, all are listed. For larger numbers, a selected sample weighted for availability of stocks, frequency of citations, and more recent citations.

Allele - Links to the Allele Report for the human or other mammalian transgene.

Transgene - Links to the Recombinant Construct Report for the human or other mammalian transgene.

Publicly Available Stocks - Links to the Stock Report for those human or mammalian transgenes available from a public stock center.

Selected Drosophila transgenes

For Drosophila gene(s) used to model this disease, transgenic constructs and associated alleles presented as a table that consists of three columns (below). All alleles of transgenic constructs associated with a disease ontology term are listed. Additional listings weighted for availability of stocks, frequency of citations, and more recent citations.

Allele - Links to the Allele Report for the Drosophila transgene.

Transgene - Links to the Recombinant Construct Report for the Drosophila transgene.

Publicly Available Stocks - Links to the Stock Report for those Drosophila transgenes available from a public stock center.

RNAi constructs available

For Drosophila gene(s) used to model this disease, all RNAi constructs; presented as a table that consists of three columns:

Allele - Links to the Allele Report for the RNAi construct.

Transgene - Links to the Recombinant Construct Report for the RNAi construct.

Publicly Available Stocks - Links to the Stock Report for those RNAi constructs available from a public stock center.

Selected Drosophila classical alleles

For Drosophila gene(s) used to model this disease, alleles presented as a table that consists of four columns (below). All classical alleles associated with a disease ontology term and/or described as amorphic are listed; if no amorphic alleles have been reported, loss-of-function alleles are listed.

Allele - Links to the Allele Report for the Drosophila classical mutant.

Allele class - Lists the FlyBase CV term for the allele class to which the allele belongs.

Mutagen - Lists the FlyBase CV term for the mutagen responsible for the genetic lesion causing the mutation.

Publicly Available Stocks - Links to the Stock Report for those Drosophila classical mutants available from a public stock center.

References

A list of publications that discuss the human disease model, subdivided into fields by type of publication.