Del(2Hoxd8,Hoxd9-Hoxd13)1Cx Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Del(2Hoxd8,Hoxd9-Hoxd13)1Cx
deletion, Chr 2, Cox 1
MGI:3574363

3 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Del(2Hoxd8,Hoxd9-Hoxd13)1Cx/Del(2Hoxd8,Hoxd9-Hoxd13)1Cx involves: NZW/LacJ	abnormal ventral spinal root morphology	J:103924
	hindlimb paralysis	J:103924
	muscular atrophy	J:103924

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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