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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Hmx1
H6 homeobox 1
MGI:107178
17 phenotypes from 3 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Hmx1dmbo/Hmx1dmbo
involves: C3HeB/FeJ * C57BL/6J
abnormal ear position J:100332
abnormal retrotympanic process morphology J:147782
normal behavior/neurological phenotype J:147782
normal craniofacial phenotype J:147782
decreased body weight J:147782
enlarged gonial bone J:147782
exencephaly J:147782
gonial bone hyperplasia J:147782
normal hearing/vestibular/ear phenotype J:147782
lowered ear position J:100332
microphthalmia J:147782
neonatal lethality, incomplete penetrance J:147782
perinatal lethality, incomplete penetrance J:147782
normal skeleton phenotype J:147782
Hmx1mpe/Hmx1mpe
C3H/HeJ-Hmx1mpe/J
abnormal ear position J:147782
decreased body size J:147782
lowered ear position J:147782
perinatal lethality, incomplete penetrance J:147782
Hmx1tm1.1Arte/Hmx1tm1.1Arte
H2az2Tg(Wnt1-cre)11Rth/H2az2+
involves: BALB/c * C57BL/6J * CBA/J
abnormal innervation J:198834
abnormal neuron differentiation J:198834

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
11/19/2024
MGI 6.24
The Jackson Laboratory