|
Symbol Name ID |
Mfsd8
major facilitator superfamily domain containing 8 MGI:1919425 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cerebral atrophy |
Cerebellar atrophy |
Neurodegeneration |
Ataxia |
EEG abnormality |
Delayed speech and language development |
Mental deterioration |
Sleep abnormality |
Global developmental delay |
Generalized myoclonic seizure |
| Disease(s) Associated with MFSD8 | ||||||||||
| neuronal ceroid lipofuscinosis 7 |
| Mouse Phenotypes | microgliosis |
CNS inflammation |
abnormal nervous system morphology |
astrocytosis |
retina photoreceptor degeneration |
|
| Availability | Mouse Genotype | |||||
| Mfsd8tm1a(EUCOMM)Hmgu/Mfsd8tm1a(EUCOMM)Hmgu | ||||||
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