E9Q7S3 · E9Q7S3_MOUSE
- ProteinCytochrome b-245, beta polypeptide
- GeneCybb
- StatusUniProtKB unreviewed (TrEMBL)
- Organism
- Amino acids
- Protein existenceEvidence at protein level
- Annotation score1/5
Publications for E9Q7S3
The central role of CD4(+) T cells in the antitumor immune response.
- CategoriesFunction
- SourceMGI: 88574
Use of RDA analysis of knockout mice to identify myeloid genes regulated in vivo by PU.1 and C/EBPalpha.
- CategoriesSequences, Expression
- SourceMGI: 88574
Ischemic stroke injury is reduced in mice lacking a functional NADPH oxidase.
- CategoriesFunction, Phenotypes & Variants
- SourceMGI: 88574
Mice lacking reduced nicotinamide adenine dinucleotide phosphate oxidase activity show increased susceptibility to early infection with Listeria monocytogenes.
- CategoriesFunction, Phenotypes & Variants
- SourceMGI: 88574
- PubMed
- Europe PMC
- J Immunol 158:5581-5583 ()
Mapped toRetroviral-mediated gene transfer of gp91phox into bone marrow cells rescues defect in host defense against Aspergillus fumigatus in murine X- linked chronic granulomatous disease.
- CategoriesSequences, Phenotypes & Variants
- SourceMGI: 88574
- PubMed
- Europe PMC
- Blood 89:41-48 ()
Mapped toCharacterization and mapping of the mouse NDP (Norrie disease) locus (Ndp).
- CategoriesSequences
- SourceMGI: 88574
Cloning of murine gp91phox cDNA and functional expression in a human X- linked chronic granulomatous disease cell line.
- CategoriesSequences
- SourceMGI: 88574
- PubMed
- Europe PMC
- Blood 87:2005-2010 ()
High-resolution comparative mapping of the proximal region of the mouse X chromosome.
- CategoriesSequences
- SourceMGI: 88574
Mapping of a liver phosphorylase kinase alpha-subunit gene on the mouse X chromosome.
- CategoriesSequences
- SourceMGI: 88574
Partial inversion of gene order within a homologous segment on the X chromosome.
- CategoriesSequences
- SourceMGI: 88574
Essential functions of synapsins I and II in synaptic vesicle regulation.
- CategoriesFunction, Phenotypes & Variants
- SourceMGI: 88574
Mouse model of X-linked chronic granulomatous disease, an inherited defect in phagocyte superoxide production.
- CategoriesFunction, Phenotypes & Variants
- SourceMGI: 88574
Genetic analyses of tattered, an X-linked dominant, developmental mouse mutation.
- CategoriesSequences
- SourceMGI: 88574
VEO-IBD NOX1 variant highlights a structural region essential for NOX/DUOX catalytic activity.
- CategoriesPhenotypes & Variants
- SourceMGI: 88574