Isx Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Isx
intestine specific homeobox
MGI:1918847

10 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Isx^{em1(IMPC)Ccpcz}/Isx^{em1(IMPC)Ccpcz} C57BL/6NCrl-Isx^{em1(IMPC)Ccpcz}/Ccpcz	abnormal bone structure	J:211773
	abnormal seminal vesicle morphology	J:211773
	abnormal skin morphology	J:211773
	abnormal spleen morphology	J:211773
	abnormal thymus morphology	J:211773
	abnormal tooth color	J:211773
	enlarged seminal vesicle	J:211773
	enlarged thymus	J:211773
Isx^tm1Shiv/Isx^tm1Shiv involves: 129S6/SvEvTac	no abnormal phenotype detected	J:119560
Tg(CAG-Isx)1Sse/? Tg(CAG-cre)13Miya/? involves: C57BL/6	perinatal lethality, incomplete penetrance	J:132176

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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