Symbol Name ID |
Slc7a8
solute carrier family 7 (cationic amino acid transporter, y+ system), member 8 MGI:1355323 |
! | Indicates phenotype varies with strain background. |
Darker colors indicate more annotations |
Mouse Phenotypes | cochlear hair cell degeneration |
abnormal spiral ligament morphology |
abnormal spiral ligament fibrocyte morphology |
abnormal strial basal cell morphology |
abnormal auditory brainstem response waveform shape |
increased or absent threshold for auditory brainstem response |
impaired hearing |
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Availability | Mouse Genotype | |||||||
Slc7a8tm1Geno/Slc7a8tm1Geno | ! | |||||||
Slc7a8tm1Geno/Slc7a8+ |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 08/02/2024 MGI 6.24 |
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