Symbol Name ID |
Pjvk
pejvakin MGI:2685847 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Sensorineural hearing impairment |
Disease(s) Associated with PJVK | |
autosomal recessive nonsyndromic deafness 59 |
Mouse Phenotypes | hearing/vestibular/ear phenotype |
abnormal auditory brainstem response |
abnormal auditory brainstem response waveform shape |
increased or absent threshold for auditory brainstem response |
|
Availability | Mouse Genotype | ||||
Pjvkem1(IMPC)J/Pjvkem1(IMPC)J | |||||
Pjvksti/Pjvksti | |||||
Pjvktm1Ugds/Pjvktm1Ugds | * |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 08/21/2024 MGI 6.24 |
![]() |
|