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Gene details
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In the results panel on the right, Gravity is adding a **Gene details** tab.

.. figure:: images/results/gene_details.png
  :figclass: align-center

General informations (1 in figure)
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The top of the *gene details* panel display the gene name and some quick links for the BioGPS, OMIM and GTEx of the gene.
Additionaly the list of pathway / gene lists to which the selected gene belong are displayed in the box below.

.. note::
  When using a GEMINI database as an input, more informations such as other names for the gene or fullname or chromosome.

Variants (2 in figure)
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Then, there is a list of all the variants carried in the gene that passes the filter set in the control panel. This list of variants can be sorted using a variable from the dropdown list just above.

For each variants, several informations are displayed:

* a sign carrying several informations
  * color: same color code as for the functional impact on the network.
  * transmission by the mother (venus), father (mars), both (mars & venus), unknown (?), *de novo* (star) (alternatively in comparison mode, A, B or both to represent the carrier)
* the HGVSp annotation when available
* genotype of the individual and of his/her parents when available
* a field reserved for the deleteriousness score used (in this documentation, see the deleteriousness part in the Settings)
* frequencies in the general population and in the current cohort

A single click on a variant will copy the position (chr:position) of the variant. A double click will open in the system default web browser a configurable link for instance a web IGV with your BAM files (in this documentation, see the BAM server part in the Settings).

Enrichment (3 in figure)
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At the bottom of this panel, there is a box plot to compare the number of variants per individual for the currently selected genes (could be multiple) accross the cohort divided into 4 categories: affected, unaffected, parents and controls. The first 3 categories are deduced from the pedigree file, the last one is optional and can be provided as a seventh column in the pedigree file (with 2 for controls, 1 for non controls, but any other value will be considered as non control).

Under the categories (other than affected) there is an indicative p-value from the *Mann-Whitney U test* betwwen the category and the affected. Those p-values are **not** corrected for multiple testing.

.. note::
  For GEMINI database a column called Control must be added to Sample table. It must have 1 for non controls, 2 for controls any other value would be considered non controls.