The IMPC applies a panel of phenotyping screens to characterise single-gene knockout mice by comparison to wild types. Click on the different tabs to visualise significant phenotypes identified by the IMPC, as well as all data that was measured.
Images submitted by IMPC centres for a selection of procedures. Each set of images is available to view in our image comparator.
The analysis uses data from IMPC, along with published data on other mouse mutants, in comparison to human disease reports in OMIM, Orphanet, and DECIPHER.
Phenotype comparisons summarize the similarity of mouse phenotypes with human disease phenotypes.
The table below shows human diseases associated to Dalrd3 by orthology or direct annotation.
The table below shows human diseases predicted to be associated to Dalrd3 by phenotypic similarity.
||Bipolar affective disorder||OMIM:152420|
|Major Affective Disorder 2||
||Bipolar affective disorder||OMIM:309200|
|Panic Disorder 1||
|Mental Retardation, Autosomal Recessive 25||
|Major Affective Disorder 1||
|Severe Primary Trimethylaminuria||
||Negative affectivity, Low self esteem, Aggressive behavior, Depression, Emotional lability, Anxiety||ORPHA:468726|
||Skin-picking, Anxiety, Depression||OMIM:164230|
|Intellectual Developmental Disorder, X-Linked 63||
|Chorea, Benign Hereditary||
||Claustrophobia, Depression, Agoraphobia, Separation insecurity, Emotional lability, Impulsivity, ...||ORPHA:66624|
|Non-Specific Early-Onset Epileptic Encephalopathy||
|Developmental And Epileptic Encephalopathy 86||
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|MGI Allele||Allele Type||Produced|