Symbol Name ID |
Pls1
plastin 1 (I-isoform) MGI:104809 |
Darker colors indicate more annotations |
Human Phenotypes | Motor delay |
Positive Romberg sign |
Disease(s) Associated with PLS1 | ||
autosomal dominant nonsyndromic deafness 76 |
Mouse Phenotypes | abnormal inner hair cell stereociliary bundle morphology |
decreased inner hair cell stereocilia number |
short inner hair cell stereocilia |
abnormal outer hair cell stereociliary bundle morphology |
fused outer hair cell stereocilia |
thin cochlear hair cell stereocilia |
abnormal hair cell mechanoelectric transduction |
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Availability | Mouse Genotype | |||||||
Pls1tm1Fri/Pls1tm1Fri |
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 09/03/2024 MGI 6.24 |
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