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Symbol
Name
ID

Lama5
laminin, alpha 5
MGI:105382

Phenotype annotations related to craniofacial

Darker colors indicate more annotations

Human Phenotypes	Decreased calvarial ossification	Relative macrocephaly	Depressed nasal bridge
Disease(s) Associated with LAMA5
bent bone dysplasia syndrome 2

Mouse Phenotypes		absent neurocranium	abnormal tooth development	lowered ear position
Availability	Mouse Genotype	absent neurocranium	abnormal tooth development	lowered ear position
	Lama5^b2b2966.1Clo/Lama5^b2b2966.1Clo
	Lama5^tm1Jhm/Lama5^tm1Jhm
	Lama5^Gt1Jhm/Lama5⁺
	Lama5^tm1Jhm/Lama5⁺

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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