Gap43 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Gap43
growth associated protein 43
MGI:95639

15 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Gap43^{tm1a(EUCOMM)Wtsi}/Gap43⁺ B6JTyr;B6N-Gap43^{tm1a(EUCOMM)Wtsi}/Wtsi	decreased body weight	J:165965
	increased body weight	J:165965
Gap43^tm1Kmr/Gap43^tm1Kmr 129/Sv-Gap43^tm1Kmr	abnormal axon extension	J:56646
	abnormal axon guidance	J:56646
	abnormal cerebral cortex morphology	J:56646
	decreased survivor rate	J:56646
	disorganized barrel cortex	J:56646
	postnatal lethality, complete penetrance	J:56646
Gap43^tm1Kmr/Gap43^tm1Kmr B6.129S1-Gap43^tm1Kmr	abnormal axon extension	J:56646
	abnormal axon guidance	J:56646
	abnormal cerebral cortex morphology	J:56646
	abnormal neuronal precursor proliferation	J:126908
	decreased survivor rate	J:56646
	disorganized barrel cortex	J:56646
	postnatal lethality, incomplete penetrance	J:56646
Gap43^tm1Mcf/Gap43^tm1Mcf involves: 129S4/SvJae * C57BL/6	abnormal axon morphology	J:110804
	abnormal optic nerve innervation	J:22966, J:110804, J:110816
	absent optic tract	J:110804, J:110816
	decreased body weight	J:22966
	increased optic chiasm size	J:22966
	postnatal lethality, incomplete penetrance	J:22966
	premature death	J:22966

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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