Lhx5 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Lhx5
LIM homeobox protein 5
MGI:107792

23 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Lhx5^{em1(IMPC)Ccpcz}/Lhx5⁺ C57BL/6N-Lhx5^{em1(IMPC)Ccpcz}/Ccpcz	abnormal heart morphology	J:211773
	abnormal seminal vesicle morphology	J:211773
	abnormal spleen morphology	J:211773
	abnormal thymus morphology	J:211773
	abnormal tooth morphology	J:211773
	enlarged heart	J:211773
	enlarged spleen	J:211773
	enlarged thymus	J:211773
	increased leukocyte cell number	J:211773
	small seminal vesicle	J:211773
Lhx5^{em1(IMPC)Ccpcz}/Lhx5^{em1(IMPC)Ccpcz} C57BL/6N-Lhx5^{em1(IMPC)Ccpcz}/Ccpcz	no spontaneous movement	J:211773
	preweaning lethality, complete penetrance	J:211773
Lhx5^tm1Lmgd/Lhx5^tm1Lmgd involves: 129S1/Sv * 129X1/SvJ * CD-1	abnormal Ammon gyrus morphology	J:55103
	abnormal axon guidance	J:55103
	abnormal hippocampus development	J:55103
	abnormal neuronal migration	J:55103
	abnormal neuronal precursor proliferation	J:55103
	absent choroid plexus	J:55103
	absent dentate gyrus	J:55103
	absent hippocampal commissure	J:55103
	absent hippocampal fimbria	J:55103
	cyanosis	J:55103
	postnatal lethality, complete penetrance	J:55103

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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