|
Symbol Name ID |
Nme5
NME/NM23 family member 5 MGI:1922783 |
| Darker colors indicate more annotations |
| Human Phenotypes | Morphological central nervous system abnormality |
Hydrocephalus |
Ventriculomegaly |
Delayed speech and language development |
| Disease(s) Associated with NME5 | ||||
| primary ciliary dyskinesia |
| Mouse Phenotypes | intraventricular hemorrhage |
hydrocephaly |
|
| Availability | Mouse Genotype | ||
| Nme5tm1Lex/Nme5tm1Lex | |||
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 05/07/2024 MGI 6.23 |
|
|
|
||
Analysis Tools