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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Hoxa2
homeobox A2
MGI:96174
19 phenotypes from multigenic genotypes
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Hoxa1tm1Mrc/Hoxa1tm2Mrc
Hoxa2tm1Mrc/Hoxa2+
involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ
abnormal basioccipital bone morphology J:58093
abnormal cranium morphology J:58093
absent stapes J:58093
neonatal lethality, complete penetrance J:58093
respiratory failure J:58093
small ears J:58093
small middle ear ossicles J:58093
Hoxa1tm2Mrc/Hoxa1+
Hoxa2tm1Mrc/Hoxa2+
involves: 129S1/Sv * 129X1/SvJ
no abnormal phenotype detected J:58093
Hoxa1tm2Mrc/Hoxa1+
Hoxa2tm1Mrc/Hoxa2tm1Mrc
involves: 129S1/Sv * 129X1/SvJ
abnormal suckling behavior J:58093
cleft secondary palate J:58093
neonatal lethality, complete penetrance J:58093
Hoxa1tm2Mrc/Hoxa1tm2Mrc
Hoxa2tm1Mrc/Hoxa2tm1Mrc
involves: 129S1/Sv * 129X1/SvJ
abnormal hindbrain morphology J:58093
abnormal middle ear ossicle morphology J:58093
absent outer ear J:58093
neonatal lethality, complete penetrance J:58093
small middle ear ossicles J:58093
Hoxa2tm1.1Fmr/Hoxa2tm1.1Fmr
Tg(CAG-cre/ERT2)F34Fmr/0
involves: 129/Sv * C57BL/6 * CD-1
no abnormal phenotype detected J:102845
Hoxa2tm1Grid/Hoxa2tm1Grid
Satb2tm1Rug/Satb2tm1Rug
involves: 129S1/Sv
normal skeleton phenotype J:115876
Hoxa2tm1Ipc/Hoxa2tm1Ipc
Hoxb2tm1Fmr/Hoxb2tm1Fmr
involves: 129/Sv * 129S2/SvPas
abnormal rhombomere morphology J:54652
increased rhombomere 1 size J:54652
neonatal lethality, complete penetrance J:54652
Hoxa2tm2.1Fmr/Hoxa2tm2.1Fmr
Hoxb2tm2.2Fmr/Hoxb2tm2.2Fmr
involves: 129S2/SvPas * C57BL/6 * SJL
abnormal brain development J:193058
decreased oligodendrocyte progenitor number J:193058
increased oligodendrocyte progenitor number J:193058

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
04/30/2024
MGI 6.23
The Jackson Laboratory