Not currently registered for phenotyping at IMPC
Phenotyping is currently not planned for a knockout strain of this gene.
Gene Summary
IMPC Data Collections
- No Body Weight Data
- No Embryo Imaging Data
- No Viability Data
Phenotyping is currently not planned for a knockout strain of this gene.
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 Mcpt1 by phenotypic similarity.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Myelolymphatic Insufficiency | Recurrent bacterial infections, Leukopenia, Recurrent viral infections, Hyposegmentation of neutr... | OMIM:310350 | |
Neutropenia-Monocytopenia-Deafness Syndrome | Abnormality of neutrophils, Abnormal macrophage morphology | ORPHA:2690 | |
Specific Granule Deficiency 1 | Recurrent pneumonia, Increased neutrophil mitochondria, Increased neutrophil ribosomes, Recurrent... | OMIM:245480 | |
Neutropenia, Severe Congenital, 1, Autosomal Dominant | Acute monocytic leukemia, Congenital agranulocytosis, Thrombocytosis, Increased circulating antib... | OMIM:202700 | |
Chronic Myeloid Leukemia | Abnormal granulocyte morphology, Leukocytosis, Splenomegaly, Abnormal basophil morphology, Thromb... | ORPHA:521 |
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MGI Allele | Allele Type | Produced |
---|---|---|
Mcpt1tm1a(EUCOMM)Hmgu | KO first allele (reporter-tagged insertion with conditional potential) | Targeting vectors, ES Cells |
Mcpt1tm1(KOMP)Vlcg | Reporter-tagged deletion allele (with selection cassette) | ES Cells |
Mcpt1tm212810(L1L2_Bact_P) | Reporter-tagged deletion allele (with selection cassette) | Targeting vectors |
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