Gene Summary
IMPC Data Collections
- Body Weight Measurements
- No Embryo Imaging Data
- Viability Data
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.
Phenotype | System | Allele | Zyg | Sex | Life Stage | P Value |
---|---|---|---|---|---|---|
small liver | Garem1em1(IMPC)Mbp | HOM | Early adult | 0.00 | ||
abnormal kidney morphology | Garem1em1(IMPC)Mbp | HOM | Early adult | 0.00 | ||
abnormal spleen morphology | Garem1em1(IMPC)Mbp | HOM | Early adult | 0.00 | ||
small spleen | Garem1em1(IMPC)Mbp | HOM | Early adult | 0.00 | ||
small kidney | Garem1em1(IMPC)Mbp | HOM | Early adult | 0.00 | ||
abnormal skin morphology | Garem1em1(IMPC)Mbp | HOM | Early adult | 0.00 | ||
abnormal liver morphology | Garem1em1(IMPC)Mbp | HOM | Early adult | 0.00 | ||
decreased body length | Garem1em1(IMPC)Mbp | HOM | Early adult | 2.05×10-05 |
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 Garem1 by phenotypic similarity.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Immunodeficiency 80 With Or Without Congenital Cardiomyopathy | Reduced natural killer cell count, Hypoplasia of the thymus, Impaired lymphocyte transformation w... | OMIM:619313 | |
Stormorken Syndrome | Howell-Jolly bodies, Hematuria, Thrombocytopenia, Anemia, Asplenia, Hypoplastic spleen | OMIM:185070 | |
Lissencephaly Syndrome, Norman-Roberts Type | Hypoplastic spleen | ORPHA:89844 | |
Gracile Bone Dysplasia | Micropenis, Asplenia, Hypoplastic spleen | OMIM:602361 | |
Ciliary Dyskinesia, Primary, 53 | Abdominal situs inversus, Hypoplastic spleen, Polysplenia | OMIM:620642 | |
Mirage Syndrome | Microphallus, Lymphopenia, Leukopenia, Hypoplastic spleen, Thrombocytopenia, Anemia, Hypospadias | OMIM:617053 | |
Pearson Syndrome | Pancytopenia, Hepatic steatosis, Neutropenia, Hepatomegaly, Hypoplastic spleen, Abnormality of th... | ORPHA:699 | |
Microphthalmia, Syndromic 9 | Renal hypoplasia, Multilobulated spleen, Horseshoe kidney, Hydronephrosis, Hypoplastic spleen, Pe... | OMIM:601186 |
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MGI Allele | Allele Type | Produced |
---|---|---|
Garem1tm1e(EUCOMM)Wtsi | Targeted, non-conditional allele | ES Cells |
Garem1tm1a(EUCOMM)Wtsi | KO first allele (reporter-tagged insertion with conditional potential) | Targeting vectors, ES Cells |
Garem1em1(IMPC)Mbp | Exon Deletion | Mice |
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