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 |
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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) |
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last database update 05/28/2024 MGI 6.13 |
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