|
Symbol Name ID |
Lamb1
laminin B1 MGI:96743 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Occipital encephalocele |
Spastic paraplegia |
Hypoplasia of the brainstem |
Hydrocephalus |
Subcortical band heterotopia |
Type II lissencephaly |
Abnormal cerebral white matter morphology |
Hypoplasia of the corpus callosum |
Leukoencephalopathy |
Porencephalic cyst |
Cerebellar vermis hypoplasia |
Cerebellar hemisphere hypoplasia |
Gray matter heterotopia |
EEG abnormality |
Abnormal nonverbal communicative behavior |
Delayed speech and language development |
Lack of spontaneous play |
Impaired ability to form peer relationships |
Autism |
Inflexible adherence to routines |
Motor stereotypy |
Restrictive behavior |
Intellectual disability |
Global developmental delay |
Severe global developmental delay |
Motor delay |
Seizure |
| Disease(s) Associated with LAMB1 | |||||||||||||||||||||||||||
| autistic disorder | |||||||||||||||||||||||||||
| lissencephaly 5 |
| Mouse Phenotypes | nervous system phenotype |
abnormal single cell response |
|
| Availability | Mouse Genotype | ||
| Lamb1Lt/Lamb1+ | * | ||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/30/2024 MGI 6.23 |
|
|
|
||
Analysis Tools