Mtch2 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Mtch2
mitochondrial carrier 2
MGI:1929260

14 phenotypes from 4 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Mtch2^tm1Atgr/Mtch2^tm1Atgr involves: 129S1/Sv * 129X1/SvJ * ICR	abnormal embryo development	J:209127
	abnormal gastrulation	J:209127
	abnormal mesoderm development	J:209127
	absent amnion	J:209127
	absent chorion	J:209127
	absent mesoderm	J:209127
	decreased embryo size	J:209127
	disorganized extraembryonic tissue	J:209127
	embryonic lethality between implantation and placentation, complete penetrance	J:209127
Mtch2^{tm1b(EUCOMM)Hmgu}/Mtch2⁺ C57BL/6N-Mtch2^{tm1b(EUCOMM)Hmgu}/Cnrm	abnormal vertebrae morphology	J:211773
	increased monocyte cell number	J:211773
Mtch2^{tm1b(EUCOMM)Hmgu}/Mtch2^{tm1b(EUCOMM)Hmgu} C57BL/6N-Mtch2^{tm1b(EUCOMM)Hmgu}/Cnrm	embryonic lethality prior to tooth bud stage	J:211773
	preweaning lethality, complete penetrance	J:211773
Mtch2^tm2Atgr/Mtch2^tm2.1Atgr Speer6-ps1^{Tg(Alb-cre)21Mgn}/Speer6-ps1⁺ involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA	liver failure	J:209127

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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