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.
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 predicted to be associated to Abhd13 by phenotypic similarity.
|Immunodeficiency 80 With Or Without Congenital Cardiomyopathy||
||T lymphocytopenia, Impaired lymphocyte transformation with phytohemagglutinin, Hypoplasia of the ...||OMIM:619313|
|Lissencephaly Syndrome, Norman-Roberts Type||
|Gracile Bone Dysplasia||
||Hypoplastic spleen, Asplenia||OMIM:602361|
||Lymphopenia, Thrombocytopenia, Anemia, Leukopenia, Hypoplastic spleen||OMIM:617053|
||Exocrine pancreatic insufficiency, Reticulocytosis, Hepatic steatosis, Macronodular cirrhosis, Ne...||ORPHA:699|
|Microphthalmia, Syndromic 9||
||Hypoplastic spleen, Multilobulated spleen||OMIM:601186|
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|MGI Allele||Allele Type||Produced|
|Abhd13tm1a(KOMP)Wtsi||KO first allele (reporter-tagged insertion with conditional potential)||Targeting vectors, ES Cells|
|Abhd13em1(IMPC)Mbp||Exon Deletion||Mice, Tissue|