Hmgn2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Hmgn2
high mobility group nucleosomal binding domain 2
MGI:96136

7 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
\Hmgn2^tm1.1Mbus/\Hmgn2^tm1.1Mbus involves: 129S4/SvJae * C57BL/6J * FVB/N	normal mortality/aging	J:211251
\Hmgn2^{tm1b(KOMP)Wtsi}/\Hmgn2^{tm1b(KOMP)Wtsi} C57BL/6N-Hmgn2^{tm1b(KOMP)Wtsi}/MbpMmucd	abnormal embryo size	J:211773
\Hmgn2^{tm1b(KOMP)Wtsi}/\Hmgn2^{tm1b(KOMP)Wtsi} C57BL/6NCrl-Hmgn2^{tm1b(KOMP)Wtsi}/MbpMmucd	preweaning lethality, incomplete penetrance	J:211773
\Tg(KRT14-Hmgn2)#Baam/0 Not Specified	abnormal enamel morphology	J:203117
	short incisors	J:203117
	short lower incisors	J:203117
	short upper incisors	J:203117

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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