Symbol Name ID |
Flnb
filamin, beta MGI:2446089 |
Darker colors indicate more annotations |
Human Phenotypes | Encephalocele |
Hypoplasia of the corpus callosum |
Spina bifida occulta |
Spinal cord compression |
Intellectual disability |
Disease(s) Associated with FLNB | |||||
atelosteogenesis | |||||
clubfoot | |||||
Larsen syndrome |
Mouse Phenotypes | abnormal middle cerebral artery morphology |
abnormal brain vasculature morphology |
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Availability | Mouse Genotype | ||
FlnbGt(BGB085)Byg/FlnbGt(BGB085)Byg |
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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