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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 | Lack of spontaneous play |
Impaired ability to form peer relationships |
Autism |
Inflexible adherence to routines |
Motor stereotypy |
Restrictive behavior |
| Disease(s) Associated with LAMB1 | ||||||
| autistic disorder |
| Mouse Phenotypes | behavior/neurological phenotype |
abnormal motor capabilities/coordination/movement |
abnormal postural reflex |
limb grasping |
dystonia |
impaired coordination |
impaired swimming |
abnormal limb posture |
abnormal gait |
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| 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) |
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last database update 05/21/2024 MGI 6.23 |
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