Symbol Name ID |
Sox10
SRY (sex determining region Y)-box 10 MGI:98358 |
Darker colors indicate more annotations |
Human Phenotypes | Decreased fetal movement |
Abdominal pain |
Disease(s) Associated with SOX10 | ||
PCWH syndrome |
Mouse Phenotypes | unresponsive to tactile stimuli |
tremors |
impaired coordination |
abnormal limb posture |
abnormal locomotor behavior |
abnormal gait |
seizures |
sporadic seizures |
|
Availability | Mouse Genotype | ||||||||
Sox10gt/Sox10gt | |||||||||
Sox10tm1Weg/Sox10tm1Weg | |||||||||
Sox10tm7.1(Sox10)Weg/Sox10tm7.1(Sox10)Weg Tg(Dhh-cre)1Mejr/0 (conditional) |
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 |
|
|