Slc6a20a | solute carrier family 6 (neurotransmitter transporter), member 20A
Physiological systems
13 / 24 physiological systems tested
13 No significant impact
11 Not tested
Data collections
Gene metrics:0Significant phenotypes
1Associated diseases
Expression examined in:0Adult tissues
0Embryo tissues
Human diseases caused by Slc6a20a 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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