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Symbol
Name
ID
Lamb1
laminin B1
MGI:96743
Phenotype annotations related to nervous system
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Microcephaly
Postnatal microcephaly
Occipital encephalocele
Perivascular spaces
Hypertonia
Spasticity
Spastic paraplegia
Spastic tetraparesis
Spastic tetraplegia
Hypoplasia of the brainstem
Lissencephaly
Agyria
Pachygyria
Subcortical band heterotopia
Type II lissencephaly
Polymicrogyria
Simplified gyral pattern
Abnormality of the cerebral white matter
Agenesis of corpus callosum
Hypoplasia of the corpus callosum
Leukoencephalopathy
Porencephalic cyst
Cerebellar hypoplasia
Cerebellar vermis hypoplasia
Hydrocephalus
Ventriculomegaly
Gray matter heterotopia
Gliosis
Ataxia
Intellectual disability
Intellectual disability, profound
Intellectual disability, severe
Dysarthria
Hyperreflexia
Psychomotor retardation
Global developmental delay
Profound global developmental delay
Severe global developmental delay
Motor delay
Specific learning disability
Seizures
Disease(s) Associated with LAMB1
lissencephaly

Mouse Phenotypes
nervous system phenotype
abnormal single cell response
Availability Mouse Genotype
Lamb1Lt/Lamb1+ *

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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last database update
11/05/2019
MGI 6.14
The Jackson Laboratory