Symbol Name ID |
Ppip5k2
diphosphoinositol pentakisphosphate kinase 2 MGI:2142810 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal vestibular function |
Sensorineural hearing impairment |
Disease(s) Associated with PPIP5K2 | ||
autosomal recessive nonsyndromic deafness 100 |
Mouse Phenotypes | cochlear outer hair cell degeneration |
abnormal auditory brainstem response waveform shape |
increased or absent threshold for auditory brainstem response |
impaired hearing |
|
Availability | Mouse Genotype | ||||
Ppip5k2tm1a(EUCOMM)Wtsi/Ppip5k2tm1a(EUCOMM)Wtsi | |||||
Ppip5k2tm1a(EUCOMM)Wtsi/Ppip5k2+ |
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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