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Symbol
Name
ID

Flnb
filamin, beta
MGI:2446089

Phenotype annotations related to nervous system

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	Encephalocele	Hypoplasia of the corpus callosum	Spina bifida occulta	Spinal cord compression	Intellectual disability
atelosteogenesis
clubfoot
Larsen syndrome

Mouse Phenotypes		abnormal middle cerebral artery morphology	abnormal brain vasculature morphology
Availability	Mouse Genotype
	Flnb^{Gt(BGB085)Byg}/Flnb^{Gt(BGB085)Byg}

Contributing Projects: 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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