Gene Summary
IMPC Data Collections
- Body Weight Measurements
- No Embryo Imaging Data
- Viability Data
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 Ift70b by phenotypic similarity.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Cephalin Lipidosis | Abnormality of the spleen | OMIM:212800 | |
Tuftsin Deficiency | Abnormality of the spleen | OMIM:191150 | |
Ceroid storage disease | Abnormality of the spleen | OMIM:214200 | |
Splenomegaly Syndrome With Splenic Germinal Center Hypoplasia And Reduced Circulating T Helper Cells | Hypersplenism, Splenomegaly, Pancytopenia, Decreased helper T cell proportion | OMIM:183350 | |
Asplenia, Isolated Congenital | Asplenia, Thrombocytosis, Howell-Jolly bodies | OMIM:271400 |
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