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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slc6a6
solute carrier family 6 (neurotransmitter transporter, taurine), member 6
MGI:98488
21 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Slc6a6m1Btlr/Slc6a6m1Btlr
C57BL/6J-Slc6a6m1Btlr
decreased total retina thickness J:254927
Slc6a6tm1Dhau/Slc6a6tm1Dhau
involves: 129X1/SvJ * C57BL/6J
abnormal amino acid level J:74276
abnormal vision J:74276
insulin resistance J:74276
reduced female fertility J:74276
retinal degeneration J:74276
retinal photoreceptor degeneration J:74276
Slc6a6tm1Jaz/Slc6a6tm1Jaz
involves: 129S2/SvPas * C57BL/6
abnormal cardiovascular system physiology J:135159
abnormal muscle fiber morphology J:135159
abnormal myocardial fiber morphology J:135159
decreased body weight J:135159
decreased cardiac muscle contractility J:135159
decreased heart weight J:135159
decreased skeletal muscle fiber diameter J:135159
decreased skeletal muscle weight J:135159
dilated cardiomyopathy J:135159
dilated heart left ventricle J:135159
impaired exercise endurance J:135159
muscular atrophy J:135159
small myocardial fiber J:135159
thin ventricular wall J:135159

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
06/19/2018
MGI 6.12
The Jackson Laboratory