Slc44a1 | solute carrier family 44, member 1
Physiological systems
18 / 24 physiological systems tested
6 Significantly impacted by the knock-out
Vision/eye Nervous system Behavior/neurological Integument Skeleton Cardiovascular system
12 No significant impact
6 Not tested
Data collections
Gene metrics:12Significant phenotypes
1Associated diseases
Expression examined in:51Adult tissues
0Embryo tissues
Human diseases caused by Slc44a1 mutations
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.
External links
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