|
Symbol Name ID |
B9d1
B9 protein domain 1 MGI:1351471 |
| Darker colors indicate more annotations |
| Human Phenotypes | Dandy-Walker malformation |
Microcephaly |
Encephalocele |
Oculomotor apraxia |
Hydrocephalus |
Aplasia/Hypoplasia of the corpus callosum |
Anencephaly |
Molar tooth sign on MRI |
Lobar holoprosencephaly |
Ataxia |
Gait ataxia |
Intellectual disability |
Global developmental delay |
| Disease(s) Associated with B9D1 | |||||||||||||
| Joubert syndrome 27 | |||||||||||||
| Meckel syndrome |
| Mouse Phenotypes | abnormal embryonic neuroepithelium morphology |
holoprosencephaly |
telencephalon hypoplasia |
abnormal nervous system development |
exencephaly |
|
| Availability | Mouse Genotype | |||||
| B9d1tm1a(EUCOMM)Wtsi/B9d1tm1a(EUCOMM)Wtsi | ||||||
| B9d1tm1d(EUCOMM)Wtsi/B9d1tm1d(EUCOMM)Wtsi | ||||||
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 04/23/2024 MGI 6.23 |
|
|
|
||
Analysis Tools