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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Dhx9
DExH-box helicase 9
MGI:108177
16 phenotypes from 2 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Dhx9tm1Ehl/Dhx9tm1Ehl
involves: 129S1/Sv * Black Swiss
abnormal ectoderm development J:50931
abnormal ectoplacental cone morphology J:50931
abnormal embryo development J:50931
embryonic lethality between implantation and somite formation, complete penetrance J:50931
increased ectoderm apoptosis J:50931
Dhx9tm1Ehl/Dhx9tm1Ehl
involves: 129S1/Sv * C57BL/6
abnormal embryo development J:50931
abnormal gastrulation J:50931
abnormal parietal endoderm morphology J:50931
abnormal primitive streak formation J:50931
abnormal visceral endoderm morphology J:50931
absent amnion J:50931
absent mesoderm J:50931
delayed gastrulation J:50931
normal embryo phenotype J:50931
embryonic lethality between implantation and somite formation, complete penetrance J:50931
increased ectoderm apoptosis J:50931
increased embryonic tissue cell apoptosis J:50931
Dhx9Tn(pb-Act-RFP)1.071225026-HRAZhu/Dhx9+
involves: FVB/NJ
normal immune system phenotype J:207361
Dhx9Tn(pb-Act-RFP)1.071225026-HRAZhu/Dhx9Tn(pb-Act-RFP)1.071225026-HRAZhu
involves: FVB/NJ
prenatal lethality, complete penetrance J:207361

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory