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Symbol Name ID |
Lamb2
laminin, beta 2 MGI:99916 |
| Darker colors indicate more annotations |
| Human Phenotypes | Microcephaly |
Progressive microcephaly |
Areflexia |
Hyporeflexia |
Global developmental delay |
Motor delay |
Persistent head lag |
| Disease(s) Associated with LAMB2 | |||||||
| Pierson syndrome |
| Mouse Phenotypes | abnormal Muller cell morphology |
decreased amacrine cell number |
abnormal amacrine cell morphology |
abnormal retina photoreceptor morphology |
short photoreceptor inner segment |
short photoreceptor outer segment |
abnormal retina rod cell morphology |
abnormal neuromuscular synapse morphology |
failure of neuromuscular synapse postsynaptic differentiation |
failure of neuromuscular synapse presynaptic differentiation |
abnormal miniature endplate potential |
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| Availability | Mouse Genotype | |||||||||||
| Lamb2tm1Jrs/Lamb2tm1Jrs | ||||||||||||
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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