|
Symbol Name ID |
Syne4
spectrin repeat containing, nuclear envelope family member 4 MGI:2141950 |
| Darker colors indicate more annotations |
| Human Phenotypes | Progressive sensorineural hearing impairment |
| Disease(s) Associated with SYNE4 | |
| autosomal recessive nonsyndromic deafness 76 |
| Mouse Phenotypes | abnormal cochlear outer hair cell morphology |
cochlear outer hair cell degeneration |
increased or absent threshold for auditory brainstem response |
|
| Availability | Mouse Genotype | |||
| Syne4tm1Kare/Syne4tm1Kare | ||||
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 04/16/2024 MGI 6.23 |
|
|
|
||
Analysis Tools