Symbol Name ID |
Sfxn4
sideroflexin 4 MGI:2137680 |
Darker colors indicate more annotations |
Human Phenotypes | Macrocytic anemia |
Hypersegmentation of neutrophil nuclei |
Disease(s) Associated with SFXN4 | ||
combined oxidative phosphorylation deficiency 18 |
Mouse Phenotypes | decreased leukocyte cell number |
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Availability | Mouse Genotype | |
Sfxn4tm1b(KOMP)Wtsi/Sfxn4tm1b(KOMP)Wtsi |
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 08/02/2024 MGI 6.24 |
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