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Symbol
Name
ID
Pls1
plastin 1 (I-isoform)
MGI:104809
Phenotype annotations related to nervous system
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
Availability Mouse Genotype
Pls1tm1Fri/Pls1tm1Fri

Contributing Projects:
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
04/23/2024
MGI 6.23
The Jackson Laboratory